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NCT03682822 · ClinicalTrials.gov registry record · NA

Routine Early vs Delayed Amniotomy for Preterm Pregnancies: A Randomized Open Label Trial

A NA study, sponsored by The University of Texas Health Science Center, Houston.

Terminated
Registry status
NA
Development phase
104
Enrollment target

NCT03682822 is a NA study that was terminated before completion, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 104 participants.

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The verdict

NCT03682822, a NA study, was terminated before completion, sponsored by The University of Texas Health Science Center, Houston.

TERMINATED
Registry status
NA
Development phase
104 participants
Enrollment target

Study Summary

To compare the duration of preterm induction of labor in women undergoing early vs. late or no artificial rupture of membranes (AROM). Maternal and neonatal outcomes will also be compared between the two groups.

Interventions

  • PROCEDURE Early Artificial rupture of membranes
  • PROCEDURE Delayed Artificial rupture of membranes

Trial Details

FieldValue
Enrollment Target 104 participants
Start Date 2018-11-01
Est. Completion 2020-02-24
Phase NA

What the Registry Record Tells You About NCT03682822

The ClinicalTrials.gov registry entry for NCT03682822 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 104 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Early Artificial rupture of membranes is the first listed.

NCT03682822 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03682822 about?

NCT03682822 is a clinical study titled "Routine Early vs Delayed Amniotomy for Preterm Pregnancies: A Randomized Open Label Trial". To compare the duration of preterm induction of labor in women undergoing early vs. late or no artificial rupture of membranes (AROM). Maternal and neonatal outcomes will also be compared between the two groups.

What is the current status of trial NCT03682822?

This trial is currently terminated. It is a NA study. The enrollment target is 104 participants. The study started on 2018-11-01. Estimated completion is 2020-02-24.

What interventions are being tested in trial NCT03682822?

The interventions under investigation include: Early Artificial rupture of membranes (PROCEDURE), Delayed Artificial rupture of membranes (PROCEDURE).

Who is sponsoring clinical trial NCT03682822?

This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.

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

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, or report a data error.