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NCT05216952 · ClinicalTrials.gov registry record · Phase 2

Ulipristal Acetate for Use in Early Pregnancy Loss

A Phase 2 study, sponsored by University of North Carolina, Chapel Hill.

Completed
Registry status
Phase 2
Development phase
3
Enrollment target

NCT05216952: Completed Phase 2 study, sponsored by University of North Carolina, Chapel Hill.

NCT05216952 is a Phase 2 study that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 3 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05216952, a Phase 2 study, has completed, sponsored by University of North Carolina, Chapel Hill.

COMPLETED
Registry status
Phase 2
Development phase
3 participants
Enrollment target

Study Summary

The investigators will study the feasibility of using 90mg ulipristal acetate, a selective progesterone receptor agonist, as an adjunct to 800mcg vaginal misoprostol for the medical management of early pregnancy loss. Patients will be followed to assess effective treatment of early pregnancy loss, additional interventions needed, side effects, adverse events and patient acceptability.

Primary Outcome

Measured as number of participants enrolled in study divided by number of patients screened for participation in study

Interventions

  • DRUG Ulipristal Acetate Tablets
  • DRUG Misoprostol Pill

Trial Details

FieldValue
Enrollment Target 3 participants
Start Date 2022-05-11
Est. Completion 2023-04-30
Phase Phase 2

What the finished NCT05216952 record still lists

NCT05216952 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 3 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which Ulipristal Acetate Tablets is the first listed.

NCT05216952 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05216952 about?

NCT05216952 is a clinical study titled "Ulipristal Acetate for Use in Early Pregnancy Loss". The investigators will study the feasibility of using 90mg ulipristal acetate, a selective progesterone receptor agonist, as an adjunct to 800mcg vaginal misoprostol for the medical management of early pregnancy loss. Patients will be followed to assess effective treatment of early pregnancy loss, a...

What is the current status of trial NCT05216952?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 3 participants. The study started on 2022-05-11. Estimated completion is 2023-04-30.

What interventions are being tested in trial NCT05216952?

The interventions under investigation include: Ulipristal Acetate Tablets (DRUG), Misoprostol Pill (DRUG).

Who is sponsoring clinical trial NCT05216952?

This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05216952's enrollment target sits among peer trials

3 2001st of 2000 the lowest of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT05216952, the US trial registry maintained by the National Library of Medicine. NCT05216952 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.