Pilot Evaluation of the StarGuide Next Generation SPECT/CT System
NCT07272161 · Status: ENROLLING_BY_INVITATION · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100
Last updated 2026-04-06
Summary
The goal of this pilot study is to evaluate capabilities of the StarGuide NextGen SPECT/CT system to inform future clinical use of this technology.
Conditions
- Nuclear Medicine
Interventions
- DEVICE
-
StarGuide NextGen SPECT/CT system
Within 1 hour of the participant receiving a scheduled clinical nuclear medicine procedure, a research scan will be performed with the StarGuide NextGen SPECT/CT system for detection of radiopharmaceutical uptake in the patient body. The total time for the scan will range from 20 - 60 minutes.
Sponsors & Collaborators
-
GE Healthcare
collaborator INDUSTRY - lead OTHER
Principal Investigators
-
Carrie B. Hruska, PhD · Mayo Clinic
Study Design
- Allocation
- NA
- Purpose
- DIAGNOSTIC
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-03-25
- Primary Completion
- 2027-01-31
- Completion
- 2027-01-31
- FDA Device
- Yes
Countries
- United States
Study Locations
More Related Trials
-
Clinical Data Collection On Advanced CT System
NCT05835284 ·Status: COMPLETED
-
Clinical Study of CT 5400 RT for System Validation
NCT06466577 ·Status: COMPLETED ·Phase: NA
-
Clinical Evaluation of the Carestream PRO 3543 and PRO 3543C Digital Detectors
NCT02383420 ·Status: COMPLETED ·Phase: NA
-
Investigational MRI Clinical Software and Hardware
NCT05215132 ·Status: RECRUITING ·Phase: PHASE4
-
Effectiveness and Safety of CT-guided Needle Placement in the Liver With the Aid of the ActiSight Needle Guidance System
NCT01367392 ·Status: COMPLETED ·Phase: PHASE4
-
Clinical Evaluation of the Next Generation Venue Ultrasound System, Components, and Accessories - Canada
NCT03653572 ·Status: COMPLETED ·Phase: NA
-
Prospective Use of Philips iSuite for Interventional Procedures
NCT03432936 ·Status: ENROLLING_BY_INVITATION ·Phase: NA
-
Safety of the PET-512MC Transesophageal Transducer
NCT01186380 ·Status: COMPLETED
-
Clinical Evaluation of DRX Plus 3543 and DRX Plus 3543C Digital Detectors
NCT02337959 ·Status: COMPLETED ·Phase: NA
-
Evaluation Of The GE Monitor Product Line
NCT00730119 ·Status: WITHDRAWN
-
Evaluation of the Spectra Optia PMN Cell Collection Procedure
NCT01805180 ·Status: COMPLETED ·Phase: NA
-
Monitoring of 5% Treatment Naïve Intravenous Immunoglobulin (IVIg) Primary Immunodeficiency Disease (PIDD) Patients Using the CareExchange® System: A Pilot Study Using 5% Gammaplex® IVIg in the Home Setting
NCT02176239 ·Status: COMPLETED
-
Implementing Myocardial Computed Tomographic Perfusion in a Community Hospital Setting
NCT02756234 ·Status: COMPLETED
-
Investigation of the Usability of Neutrocheck Amongst Healthy Volunteers and Healthcare Professionals.
NCT05852249 ·Status: UNKNOWN
-
Usability, Adherence and Diagnostic Performance of PointCheck in Pediatric Population
NCT04889937 ·Status: COMPLETED
-
StatStrip Lactate, Hemoglobin, and Hematocrit Meter in Whole Blood
NCT05118048 ·Status: TERMINATED
-
Effectiveness of ActiSight™ Needle Guidance System in Patients Undergoing CT-Guided Procedures
NCT01148706 ·Status: COMPLETED ·Phase: PHASE4
-
Clinical Investigation of the Safety of the MediSieve Magnetic Haemofiltration System in Healthy Volunteers
NCT05713188 ·Status: COMPLETED ·Phase: PHASE1
-
QStat Pilot Reference Range Study
NCT04490759 ·Status: COMPLETED
-
Study to Test the Usability of a New Injector to Administer Contrast Media Into Humans for Diagnostic Purposes
NCT03875469 ·Status: COMPLETED ·Phase: NA
-
Multicenter Performance Study of TriQuik Invitro Diagnostic Device
NCT05293821 ·Status: UNKNOWN
-
Evaluation of the Clinical Performance of the Quantra System With the QStat Cartridge
NCT03912545 ·Status: COMPLETED
-
Reference Range Study for the Quantra QStat System
NCT04219371 ·Status: COMPLETED
-
Evaluation of the Clinical Performance of the Quantra System With the QStat Cartridge in Trauma
NCT03934983 ·Status: COMPLETED
-
Comparative Evaluation of the FINDER Instrument and FINDER G6PD Cartridge in Adults and Neonates
NCT04146246 ·Status: COMPLETED