Trial Outcomes & Findings for EXPLORER PET/CT in Healthy Volunteers (NCT NCT04110743)

NCT ID: NCT04110743

Last Updated: 2024-11-21

Results Overview

To collect preliminary data regarding FDG biodistribution in the organs listed as a function of time of 12 hours. Time-activity curves will be created

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

30 participants

Primary outcome timeframe

approximatively 12 hours for Arm 1 only

Results posted on

2024-11-21

Participant Flow

Participant milestones

Participant milestones
Measure
Delayed Imaging Acquisition
10 mCi of 18F fluorodeoxyglucose (FDG) will be injected through the IV and a 60-minute dynamic scan will begin on EXPLORER. The IV line will be removed after dynamic acquisition. The dynamic scan will be preceded by ultra low-dose (1.298 mSv) CT scan to provide information for attenuation correction for the PET data. At 90 minutes, 3-, 6-, 9- and 12-hours, a static whole-body scan for 20 minutes will be acquired on EXPLORER. Prior to the 90-minute scan a low-dose CT (7.44 mSv) will be obtained both for anatomic localization and for attenuation correction purposes. Prior to each of the later time-points (3-, 6-, 9- and 12-hours), an ultra low-dose (1.298 mSv) CT scan will be acquired. This scan will be for attenuation correction purposes only. Following the 12-hour scan, the participant's study visit will be completed. MRI Brain will be also obtained after PET/CT scanning for anatomic correlation. EXPLORER PET/CT: Intervention: PET/CT using different protocols
Low FDG Dose Imaging
0.5 mCi of 18F-FDG (1/20th of the standard dose) will be hand injected through the IV and a 60-minute dynamic scan will begin on EXPLORER. The dynamic scan will be preceded by an ultra-low-dose CT scan (1.298 mSv) for attenuation correction. The standard 20-minute EXPLORER scan obtained at 90 minutes will be obtained after a low dose CT (7.44 mSv) for attenuation and co-localization. The standard 20-minute EXPLORER scan obtained at 3 hours will be preceded by an ultra-low-dose CT scan (1.298 mSv) for attenuation correction only. MRI Brain will be also obtained after PET/CT scanning for anatomic correlation. EXPLORER PET/CT: Intervention: PET/CT using different protocols
Comparison PET Images Reconstructed Using CT-based Attenuation
10 mCi of 18F-FDG will be hand injected through the IV and a 60-minute dynamic scan will begin on EXPLORER. Prior to the dynamic scan, an ultra-low-dose CT scan (1.298 mSv) will be acquired for attenuation correction purposes only. At 90 mins, a low dose non contrast enhancement CT (7.44 mSv) will be acquired vertex to toes. Iodinated contrast (150 cc of iodine Omnipaque 350) will then be intravenously injected (through the same IV placed to inject FDG) at 3 ml/sec while the patient remains still on the scanner and a second low-dose CT will be acquired. Finally, a 20-minute PET acquisition will be performed. The IV line will be removed after completion of the study. MRI Brain will be also obtained after PET/CT scanning for anatomic correlation. EXPLORER PET/CT: Intervention: PET/CT using different protocols
Overall Study
STARTED
15
15
0
Overall Study
COMPLETED
15
15
0
Overall Study
NOT COMPLETED
0
0
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

EXPLORER PET/CT in Healthy Volunteers

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Delayed Imaging Acquisition
n=15 Participants
10 mCi of 18F fluorodeoxyglucose (FDG) will be injected through the IV and a 60-minute dynamic scan will begin on EXPLORER. The IV line will be removed after dynamic acquisition. The dynamic scan will be preceded by ultra low-dose (1.298 mSv) CT scan to provide information for attenuation correction for the PET data. At 90 minutes, 3-, 6-, 9- and 12-hours, a static whole-body scan for 20 minutes will be acquired on EXPLORER. Prior to the 90-minute scan a low-dose CT (7.44 mSv) will be obtained both for anatomic localization and for attenuation correction purposes. Prior to each of the later time-points (3-, 6-, 9- and 12-hours), an ultra low-dose (1.298 mSv) CT scan will be acquired. This scan will be for attenuation correction purposes only. Following the 12-hour scan, the participant's study visit will be completed. MRI Brain will be also obtained after PET/CT scanning for anatomic correlation. EXPLORER PET/CT: Intervention: PET/CT using different protocols
Low FDG Dose Imaging
n=15 Participants
0.5 mCi of 18F-FDG (1/20th of the standard dose) will be hand injected through the IV and a 60-minute dynamic scan will begin on EXPLORER. The dynamic scan will be preceded by an ultra-low-dose CT scan (1.298 mSv) for attenuation correction. The standard 20-minute EXPLORER scan obtained at 90 minutes will be obtained after a low dose CT (7.44 mSv) for attenuation and co-localization. The standard 20-minute EXPLORER scan obtained at 3 hours will be preceded by an ultra-low-dose CT scan (1.298 mSv) for attenuation correction only. MRI Brain will be also obtained after PET/CT scanning for anatomic correlation. EXPLORER PET/CT: Intervention: PET/CT using different protocols
Comparison PET Images Reconstructed Using CT-based Attenuation
10 mCi of 18F-FDG will be hand injected through the IV and a 60-minute dynamic scan will begin on EXPLORER. Prior to the dynamic scan, an ultra-low-dose CT scan (1.298 mSv) will be acquired for attenuation correction purposes only. At 90 mins, a low dose non contrast enhancement CT (7.44 mSv) will be acquired vertex to toes. Iodinated contrast (150 cc of iodine Omnipaque 350) will then be intravenously injected (through the same IV placed to inject FDG) at 3 ml/sec while the patient remains still on the scanner and a second low-dose CT will be acquired. Finally, a 20-minute PET acquisition will be performed. The IV line will be removed after completion of the study. MRI Brain will be also obtained after PET/CT scanning for anatomic correlation. EXPLORER PET/CT: Intervention: PET/CT using different protocols
Total
n=30 Participants
Total of all reporting groups
Age, Categorical
<=18 years
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=7 Participants
Age, Categorical
Between 18 and 65 years
14 Participants
n=99 Participants
15 Participants
n=107 Participants
29 Participants
n=7 Participants
Age, Categorical
>=65 years
1 Participants
n=99 Participants
0 Participants
n=107 Participants
1 Participants
n=7 Participants
Age, Continuous
49.5 YEARS
n=99 Participants
45.3 YEARS
n=107 Participants
47.4 YEARS
n=7 Participants
Sex: Female, Male
Female
9 Participants
n=99 Participants
7 Participants
n=107 Participants
16 Participants
n=7 Participants
Sex: Female, Male
Male
6 Participants
n=99 Participants
8 Participants
n=107 Participants
14 Participants
n=7 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=7 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=7 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
15 Participants
n=99 Participants
15 Participants
n=107 Participants
30 Participants
n=7 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=7 Participants
Race (NIH/OMB)
Asian
0 Participants
n=99 Participants
1 Participants
n=107 Participants
1 Participants
n=7 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=7 Participants
Race (NIH/OMB)
Black or African American
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=7 Participants
Race (NIH/OMB)
White
7 Participants
n=99 Participants
10 Participants
n=107 Participants
17 Participants
n=7 Participants
Race (NIH/OMB)
More than one race
0 Participants
n=99 Participants
0 Participants
n=107 Participants
0 Participants
n=7 Participants
Race (NIH/OMB)
Unknown or Not Reported
8 Participants
n=99 Participants
4 Participants
n=107 Participants
12 Participants
n=7 Participants
Region of Enrollment
United States
15 participants
n=99 Participants
15 participants
n=107 Participants
30 participants
n=7 Participants

PRIMARY outcome

Timeframe: approximatively 12 hours for Arm 1 only

To collect preliminary data regarding FDG biodistribution in the organs listed as a function of time of 12 hours. Time-activity curves will be created

Outcome measures

Outcome measures
Measure
Delayed Imaging Acquisition
n=15 Participants
10 mCi of 18F fluorodeoxyglucose (FDG) will be injected through the IV and a 60-minute dynamic scan will begin on EXPLORER. The IV line will be removed after dynamic acquisition. The dynamic scan will be preceded by ultra low-dose (1.298 mSv) CT scan to provide information for attenuation correction for the PET data. At 90 minutes, 3-, 6-, 9- and 12-hours, a static whole-body scan for 20 minutes will be acquired on EXPLORER. Prior to the 90-minute scan a low-dose CT (7.44 mSv) will be obtained both for anatomic localization and for attenuation correction purposes. Prior to each of the later time-points (3-, 6-, 9- and 12-hours), an ultra low-dose (1.298 mSv) CT scan will be acquired. This scan will be for attenuation correction purposes only. Following the 12-hour scan, the participant's study visit will be completed. MRI Brain will be also obtained after PET/CT scanning for anatomic correlation. EXPLORER PET/CT: Intervention: PET/CT using different protocols
Arm 2
Average SUV mean at 90 minutes
Standardized Uptake Value SUV(t)= C(t)/ID/BW; C(t) is Radioactivity Measured at the Time t, Decay Corrected to t=0 and Converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; W= Body Weight; SUV is Correct UM
Aorta
0.83 SUV
Standard Deviation 0.47
Standardized Uptake Value SUV(t)= C(t)/ID/BW; C(t) is Radioactivity Measured at the Time t, Decay Corrected to t=0 and Converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; W= Body Weight; SUV is Correct UM
Lungs
0.48 SUV
Standard Deviation 0.44
Standardized Uptake Value SUV(t)= C(t)/ID/BW; C(t) is Radioactivity Measured at the Time t, Decay Corrected to t=0 and Converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; W= Body Weight; SUV is Correct UM
Liver
1.68 SUV
Standard Deviation 0.51
Standardized Uptake Value SUV(t)= C(t)/ID/BW; C(t) is Radioactivity Measured at the Time t, Decay Corrected to t=0 and Converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; W= Body Weight; SUV is Correct UM
Spleen
2.01 SUV
Standard Deviation 0.49
Standardized Uptake Value SUV(t)= C(t)/ID/BW; C(t) is Radioactivity Measured at the Time t, Decay Corrected to t=0 and Converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; W= Body Weight; SUV is Correct UM
Kidneys
1.91 SUV
Standard Deviation 0.83
Standardized Uptake Value SUV(t)= C(t)/ID/BW; C(t) is Radioactivity Measured at the Time t, Decay Corrected to t=0 and Converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; W= Body Weight; SUV is Correct UM
Bone Marrow
3.44 SUV
Standard Deviation 0.85
Standardized Uptake Value SUV(t)= C(t)/ID/BW; C(t) is Radioactivity Measured at the Time t, Decay Corrected to t=0 and Converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; W= Body Weight; SUV is Correct UM
Skeletal Muscles
1.23 SUV
Standard Deviation 0.44
Standardized Uptake Value SUV(t)= C(t)/ID/BW; C(t) is Radioactivity Measured at the Time t, Decay Corrected to t=0 and Converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; W= Body Weight; SUV is Correct UM
Subcutaneous Fat
0.25 SUV
Standard Deviation 0.21
Standardized Uptake Value SUV(t)= C(t)/ID/BW; C(t) is Radioactivity Measured at the Time t, Decay Corrected to t=0 and Converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; W= Body Weight; SUV is Correct UM
Whole Brain
5.81 SUV
Standard Deviation 1.87
Standardized Uptake Value SUV(t)= C(t)/ID/BW; C(t) is Radioactivity Measured at the Time t, Decay Corrected to t=0 and Converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; W= Body Weight; SUV is Correct UM
Myocardium
14.0 SUV
Standard Deviation 6.93

PRIMARY outcome

Timeframe: approximatively 6 hours for Arm 1 only

To obtain preliminary data regarding low dose EXPLORER noise level

Outcome measures

Outcome measures
Measure
Delayed Imaging Acquisition
n=15 Participants
10 mCi of 18F fluorodeoxyglucose (FDG) will be injected through the IV and a 60-minute dynamic scan will begin on EXPLORER. The IV line will be removed after dynamic acquisition. The dynamic scan will be preceded by ultra low-dose (1.298 mSv) CT scan to provide information for attenuation correction for the PET data. At 90 minutes, 3-, 6-, 9- and 12-hours, a static whole-body scan for 20 minutes will be acquired on EXPLORER. Prior to the 90-minute scan a low-dose CT (7.44 mSv) will be obtained both for anatomic localization and for attenuation correction purposes. Prior to each of the later time-points (3-, 6-, 9- and 12-hours), an ultra low-dose (1.298 mSv) CT scan will be acquired. This scan will be for attenuation correction purposes only. Following the 12-hour scan, the participant's study visit will be completed. MRI Brain will be also obtained after PET/CT scanning for anatomic correlation. EXPLORER PET/CT: Intervention: PET/CT using different protocols
Arm 2
Average SUV mean at 90 minutes
Coefficient of Variation. SD/Mean (Standard Deviation Divided by Mean Value)
Aorta
60.5 coefficient
Standard Deviation 14.8
Coefficient of Variation. SD/Mean (Standard Deviation Divided by Mean Value)
Lungs
140.1 coefficient
Standard Deviation 8.1
Coefficient of Variation. SD/Mean (Standard Deviation Divided by Mean Value)
Liver
32.2 coefficient
Standard Deviation 9.0
Coefficient of Variation. SD/Mean (Standard Deviation Divided by Mean Value)
Spleen
31.4 coefficient
Standard Deviation 9.3
Coefficient of Variation. SD/Mean (Standard Deviation Divided by Mean Value)
Kidneys
64.4 coefficient
Standard Deviation 18.4
Coefficient of Variation. SD/Mean (Standard Deviation Divided by Mean Value)
Bone Marrow
40.8 coefficient
Standard Deviation 11.8
Coefficient of Variation. SD/Mean (Standard Deviation Divided by Mean Value)
Skeletal Muscles
53.0 coefficient
Standard Deviation 18.8
Coefficient of Variation. SD/Mean (Standard Deviation Divided by Mean Value)
Subcutaneous Fat
88.6 coefficient
Standard Deviation 24.8
Coefficient of Variation. SD/Mean (Standard Deviation Divided by Mean Value)
Whole Brain
54.5 coefficient
Standard Deviation 8.1
Coefficient of Variation. SD/Mean (Standard Deviation Divided by Mean Value)
Myocardium
63.0 coefficient
Standard Deviation 16.7

PRIMARY outcome

Timeframe: approximatively 90 minutes

To collect preliminary data about total body FDG perfusion and early biodistribution. Time-activity curves will be created

Outcome measures

Outcome measures
Measure
Delayed Imaging Acquisition
n=15 Participants
10 mCi of 18F fluorodeoxyglucose (FDG) will be injected through the IV and a 60-minute dynamic scan will begin on EXPLORER. The IV line will be removed after dynamic acquisition. The dynamic scan will be preceded by ultra low-dose (1.298 mSv) CT scan to provide information for attenuation correction for the PET data. At 90 minutes, 3-, 6-, 9- and 12-hours, a static whole-body scan for 20 minutes will be acquired on EXPLORER. Prior to the 90-minute scan a low-dose CT (7.44 mSv) will be obtained both for anatomic localization and for attenuation correction purposes. Prior to each of the later time-points (3-, 6-, 9- and 12-hours), an ultra low-dose (1.298 mSv) CT scan will be acquired. This scan will be for attenuation correction purposes only. Following the 12-hour scan, the participant's study visit will be completed. MRI Brain will be also obtained after PET/CT scanning for anatomic correlation. EXPLORER PET/CT: Intervention: PET/CT using different protocols
Arm 2
n=15 Participants
Average SUV mean at 90 minutes
Standardized Uptake Value
Lungs
0.62 SUV
Standard Deviation 0.37
0.32 SUV
Standard Deviation 0.06
Standardized Uptake Value
Aorta
1.75 SUV
Standard Deviation 0.34
0.88 SUV
Standard Deviation 0.17
Standardized Uptake Value
Liver
2.49 SUV
Standard Deviation 0.44
1.02 SUV
Standard Deviation 0.19
Standardized Uptake Value
Spleen
2.15 SUV
Standard Deviation 0.40
0.83 SUV
Standard Deviation 0.15
Standardized Uptake Value
Kidneys
3.65 SUV
Standard Deviation 1.85
1.45 SUV
Standard Deviation 0.23
Standardized Uptake Value
Bone Marrow
2.51 SUV
Standard Deviation 0.44
0.73 SUV
Standard Deviation 0.15
Standardized Uptake Value
Skeletal Muscles
0.70 SUV
Standard Deviation 0.19
0.37 SUV
Standard Deviation 0.06
Standardized Uptake Value
Subcutaneous Fat
0.19 SUV
Standard Deviation 0.05
0.19 SUV
Standard Deviation 0.04
Standardized Uptake Value
Whole Brain
9.88 SUV
Standard Deviation 2.63
4.95 SUV
Standard Deviation 1.36
Standardized Uptake Value
Myocardium
10.73 SUV
Standard Deviation 4.92
1.20 SUV
Standard Deviation 0.80

PRIMARY outcome

Timeframe: approximatively 3 hours

To obtain preliminary data to understand whether intravenous iodinated contrast agent produce a significant change in quantification of FDG uptake levels. Time/activity curves will be generated.

Outcome measures

Outcome measures
Measure
Delayed Imaging Acquisition
n=15 Participants
10 mCi of 18F fluorodeoxyglucose (FDG) will be injected through the IV and a 60-minute dynamic scan will begin on EXPLORER. The IV line will be removed after dynamic acquisition. The dynamic scan will be preceded by ultra low-dose (1.298 mSv) CT scan to provide information for attenuation correction for the PET data. At 90 minutes, 3-, 6-, 9- and 12-hours, a static whole-body scan for 20 minutes will be acquired on EXPLORER. Prior to the 90-minute scan a low-dose CT (7.44 mSv) will be obtained both for anatomic localization and for attenuation correction purposes. Prior to each of the later time-points (3-, 6-, 9- and 12-hours), an ultra low-dose (1.298 mSv) CT scan will be acquired. This scan will be for attenuation correction purposes only. Following the 12-hour scan, the participant's study visit will be completed. MRI Brain will be also obtained after PET/CT scanning for anatomic correlation. EXPLORER PET/CT: Intervention: PET/CT using different protocols
Arm 2
n=15 Participants
Average SUV mean at 90 minutes
Standardized Uptake Value SUV(t)= C(t)/(ID/BW); C(t) is Radioactivity Measured From at Time t, Decay Corrected to t=0-converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; BW= Body Weight; SUV is Correct UM
Subcutaneous Fat
0.16 SUV
Standard Deviation 0.05
0.07 SUV
Standard Deviation 0.02
Standardized Uptake Value SUV(t)= C(t)/(ID/BW); C(t) is Radioactivity Measured From at Time t, Decay Corrected to t=0-converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; BW= Body Weight; SUV is Correct UM
Aorta
1.18 SUV
Standard Deviation 0.30
0.39 SUV
Standard Deviation 0.08
Standardized Uptake Value SUV(t)= C(t)/(ID/BW); C(t) is Radioactivity Measured From at Time t, Decay Corrected to t=0-converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; BW= Body Weight; SUV is Correct UM
Lungs
0.52 SUV
Standard Deviation 0.53
0.15 SUV
Standard Deviation 0.04
Standardized Uptake Value SUV(t)= C(t)/(ID/BW); C(t) is Radioactivity Measured From at Time t, Decay Corrected to t=0-converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; BW= Body Weight; SUV is Correct UM
Liver
2.11 SUV
Standard Deviation 0.42
0.50 SUV
Standard Deviation 0.10
Standardized Uptake Value SUV(t)= C(t)/(ID/BW); C(t) is Radioactivity Measured From at Time t, Decay Corrected to t=0-converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; BW= Body Weight; SUV is Correct UM
Spleen
2.09 SUV
Standard Deviation 0.41
0.43 SUV
Standard Deviation 0.08
Standardized Uptake Value SUV(t)= C(t)/(ID/BW); C(t) is Radioactivity Measured From at Time t, Decay Corrected to t=0-converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; BW= Body Weight; SUV is Correct UM
Kidneys
3.30 SUV
Standard Deviation 1.34
0.66 SUV
Standard Deviation 0.12
Standardized Uptake Value SUV(t)= C(t)/(ID/BW); C(t) is Radioactivity Measured From at Time t, Decay Corrected to t=0-converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; BW= Body Weight; SUV is Correct UM
Bone Marrow
2.92 SUV
Standard Deviation 0.56
0.44 SUV
Standard Deviation 0.09
Standardized Uptake Value SUV(t)= C(t)/(ID/BW); C(t) is Radioactivity Measured From at Time t, Decay Corrected to t=0-converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; BW= Body Weight; SUV is Correct UM
Skeletal Muscles
0.82 SUV
Standard Deviation 0.21
0.21 SUV
Standard Deviation 0.04
Standardized Uptake Value SUV(t)= C(t)/(ID/BW); C(t) is Radioactivity Measured From at Time t, Decay Corrected to t=0-converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; BW= Body Weight; SUV is Correct UM
Whole Brain
10.39 SUV
Standard Deviation 3.02
2.97 SUV
Standard Deviation 0.86
Standardized Uptake Value SUV(t)= C(t)/(ID/BW); C(t) is Radioactivity Measured From at Time t, Decay Corrected to t=0-converted From a Volume to a Mass Based Unit Via the Factor 1/(1 g/mL); ID: the Injected Dose at t=0; BW= Body Weight; SUV is Correct UM
Myocardium
11.60 SUV
Standard Deviation 5.92
0.68 SUV
Standard Deviation 0.59

Adverse Events

Delayed Imaging Acquisition

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Low FDG Dose Imaging

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Comparison PET Images Reconstructed Using CT-based Attenuation

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Dr. Lorenzo Nardo

University of California Davis

Phone: 916-731-9004

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place