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NCT03340701 · ClinicalTrials.gov registry record · Phase 1

Pharmacokinetics of Progesterone in Pregnancy

A Phase 1 study, sponsored by Thomas Jefferson University.

Completed
Registry status
Phase 1
Development phase
6
Enrollment target

NCT03340701: Completed Phase 1 study, sponsored by Thomas Jefferson University.

NCT03340701 is a Phase 1 study that has completed, run by Thomas Jefferson University. The registered enrollment target is 6 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03340701, a Phase 1 study, has completed, sponsored by Thomas Jefferson University.

COMPLETED
Registry status
Phase 1
Development phase
6 participants
Enrollment target

Study Summary

Pharmacokinetic analysis of 200mg vaginal progesterone suppository in women with singleton pregnancies between 18 0/7- 23 6/7 weeks' gestation

Primary Outcome

Plasma concentration time profile of vaginal progesterone in pregnant women.

Interventions

  • DRUG vaginal progesterone suppository

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2017-11-06
Est. Completion 2018-06-30
Phase Phase 1
Thomas Jefferson University

292 total trials

What the finished NCT03340701 record still lists

NCT03340701 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 6 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 1 intervention - of which vaginal progesterone suppository is the first listed.

NCT03340701 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03340701 about?

NCT03340701 is a clinical study titled "Pharmacokinetics of Progesterone in Pregnancy". Pharmacokinetic analysis of 200mg vaginal progesterone suppository in women with singleton pregnancies between 18 0/7- 23 6/7 weeks' gestation

What is the current status of trial NCT03340701?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 6 participants. The study started on 2017-11-06. Estimated completion is 2018-06-30.

What interventions are being tested in trial NCT03340701?

The interventions under investigation include: vaginal progesterone suppository (DRUG).

Who is sponsoring clinical trial NCT03340701?

This trial is sponsored by Thomas Jefferson University, which has 292 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03340701's enrollment target sits among peer trials

6 1974th of 2000 higher than 12 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03340701, the US trial registry maintained by the National Library of Medicine. NCT03340701 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.