Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT00442663 · ClinicalTrials.gov registry record · NA
Trial of Foley Catheter With and Without Extra-Amniotic Saline Infusion for Labor Induction
A NA study, sponsored by University of Alabama at Birmingham.
- Completed
- Registry status
- NA
- Development phase
- 170
- Enrollment target
NCT00442663 is a NA study that has completed, run by University of Alabama at Birmingham. The registered enrollment target is 170 participants.
The verdict
NCT00442663, a NA study, has completed, sponsored by University of Alabama at Birmingham.
- COMPLETED
- Registry status
- NA
- Development phase
- 170 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the efficacy of a transcervical Foley catheter with and without extra-amniotic saline infusion (EASI) for priming the cervix for labor.
Interventions
- DEVICE Transcervical Foley Catheter
- DEVICE Transcervical Foley Catheter with an EASI
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 170 participants |
| Start Date | 2003-06 |
| Est. Completion | 2005-12 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00442663
The ClinicalTrials.gov registry entry for NCT00442663 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 170 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Alabama at Birmingham, which has 1,160 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Transcervical Foley Catheter is the first listed.
NCT00442663 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00442663 about?
NCT00442663 is a clinical study titled "Trial of Foley Catheter With and Without Extra-Amniotic Saline Infusion for Labor Induction". The purpose of this study is to compare the efficacy of a transcervical Foley catheter with and without extra-amniotic saline infusion (EASI) for priming the cervix for labor.
What is the current status of trial NCT00442663?
This trial is currently completed. It is a NA study. The enrollment target is 170 participants. The study started on 2003-06. Estimated completion is 2005-12.
What interventions are being tested in trial NCT00442663?
The interventions under investigation include: Transcervical Foley Catheter (DEVICE), Transcervical Foley Catheter with an EASI (DEVICE).
Who is sponsoring clinical trial NCT00442663?
This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
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.