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NCT05099991 · ClinicalTrials.gov registry record · NA

Transcervical Balloon Compared to Osmotic Dilators Prior to Surgical Abortion

A NA study, sponsored by Stanford University.

Completed
Registry status
NA
Development phase
32
Enrollment target

NCT05099991: Completed NA study, sponsored by Stanford University.

NCT05099991 is a NA study that has completed, run by Stanford University. The registered enrollment target is 32 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT05099991, a NA study, has completed, sponsored by Stanford University.

COMPLETED
Registry status
NA
Development phase
32 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether a Foley balloon is similar to osmotic dilators for preparing the cervix prior to a second trimester abortion. Procedure time will be used to compare the two different methods of cervical preparation, reflecting the ease at which the surgeon can perform through a prepared cervix. The aim is to expand effective options for cervical preparation that will can accommodate for varying patient characteristics and provider experiences.

Primary Outcome

Time to speculum in to speculum out

Interventions

  • DEVICE Dilapan-S
  • DEVICE Single Foley Balloon

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 2022-02-08
Est. Completion 2023-04-28
Phase NA
Stanford University

1,744 total trials

What the finished NCT05099991 record still lists

NCT05099991 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 32 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).

The record links to 0 conditions, and to 2 interventions - of which Dilapan-S is the first listed.

NCT05099991 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05099991 about?

NCT05099991 is a clinical study titled "Transcervical Balloon Compared to Osmotic Dilators Prior to Surgical Abortion". The purpose of this study is to determine whether a Foley balloon is similar to osmotic dilators for preparing the cervix prior to a second trimester abortion. Procedure time will be used to compare the two different methods of cervical preparation, reflecting the ease at which the surgeon can perfo...

What is the current status of trial NCT05099991?

This trial is currently completed. It is a NA study. The enrollment target is 32 participants. The study started on 2022-02-08. Estimated completion is 2023-04-28.

What interventions are being tested in trial NCT05099991?

The interventions under investigation include: Dilapan-S (DEVICE), Single Foley Balloon (DEVICE).

Who is sponsoring clinical trial NCT05099991?

This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05099991's enrollment target sits among peer trials

32 1578th of 2000 higher than 409 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT05099991, the US trial registry maintained by the National Library of Medicine. NCT05099991 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.