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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. According to ClinicalTrials.gov, the official US trial registry.

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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.

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

Sponsor

Stanford University

1,744 total trials

What the Registry Record Tells You About NCT05099991

The ClinicalTrials.gov registry entry for NCT05099991 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 32 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Stanford University, which has 1,744 total studies on file at ClinicalTrials.gov.

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

NCT05099991 reports 0 study locations.

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.