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Comparison of Beta-hCG Levels When Using Venous Puncture Blood and Peripheral Finger Stick Blood

Comparison of Beta-hCG Levels When Using Venous Puncture Blood and Peripheral Finger Stick Blood

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07493720
Acronym
P-Beta-H
Enrollment
40
Registered
2026-03-25
Start date
2026-07-01
Completion date
2026-12-01
Last updated
2026-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy

Keywords

pregnancy

Brief summary

The objective of his study is to quantitatively evaluate a patient's pregnancy status using their beta-hCG levels when using venipuncture blood vs peripheral blood.

Detailed description

The objective of his study is to quantitatively evaluate a patient's pregnancy status using their beta-hCG levels when using venipuncture blood vs peripheral blood. This data will help the investigator compare trending levels of beta-hCG levels in pregnant patients between venous blood vs peripheral blood which may help determine levels at which the peripheral blood may no longer be detectable on a POC pregnancy test.

Interventions

DIAGNOSTIC_TESTBeta-hCG

Enrolled participants will provide 2 serum specimens (venipuncture and peripheral finger stick) for beta-hCG testing

Sponsors

University of Nebraska
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

19 years of age, positive pregnant status recorded in EMR, presenting to Nebraska Medicine OB/GYN clinic -

Exclusion criteria

No meeting the inclusion criteria \-

Design outcomes

Primary

MeasureTime frameDescription
Beta-hCG valueOnce on date of enrollmentVenipuncture and peripheral finger stick serum will be tested for beta-hCG levels.

Countries

United States

Contacts

CONTACTThanh Nguyen, PhD
thang.nguyen@unmc.edu14025597884

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 26, 2026