Trial Outcomes & Findings for Efficacy Evaluation of Using Finger Stick Peripheral Blood for Point of Care Pregnancy Testing (NCT NCT06747598)
NCT ID: NCT06747598
Last Updated: 2026-05-12
Results Overview
A peripheral serum sample was collected through a finger stick point-of-care (POC) test to assess pregnancy in 30 women with previously confirmed pregnancies. The results were reported as either positive or negative.
COMPLETED
30 participants
One time test at time of enrollment
2026-05-12
Participant Flow
Participant milestones
| Measure |
POC Serum Pregnancy Test Arm
Enrolled participants will provide a peripheral serum specimen for POC pregnancy testing
|
|---|---|
|
Overall Study
STARTED
|
30
|
|
Overall Study
COMPLETED
|
30
|
|
Overall Study
NOT COMPLETED
|
0
|
Reasons for withdrawal
Withdrawal data not reported
Baseline Characteristics
specific patient age not collected, only confirmed age was 19 yrs or older
Baseline characteristics by cohort
| Measure |
POC Serum Pregnancy Test Arm
n=30 Participants
Enrolled participants will provide a peripheral serum specimen for POC pregnancy testing
|
|---|---|
|
Age, Customized
Age
|
30 Participants
n=30 Participants • specific patient age not collected, only confirmed age was 19 yrs or older
|
|
Sex/Gender, Customized
Female
|
30 Participants
n=30 Participants
|
PRIMARY outcome
Timeframe: One time test at time of enrollmentPopulation: All 30 peripheral serum specimens tested positive for pregnancy.
A peripheral serum sample was collected through a finger stick point-of-care (POC) test to assess pregnancy in 30 women with previously confirmed pregnancies. The results were reported as either positive or negative.
Outcome measures
| Measure |
POC Serum Pregnancy Test Arm
n=30 Participants
Enrolled participants will provide a peripheral serum specimen for POC pregnancy testing
|
|---|---|
|
Number of Participants With Positive POC Serum Pregnancy Test
|
30 Participants
|
Adverse Events
POC Serum Pregnancy Test Arm
Serious adverse events
Adverse event data not reported
Other adverse events
Adverse event data not reported
Additional Information
Results disclosure agreements
- Principal investigator is a sponsor employee
- Publication restrictions are in place