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NCT00565383 · ClinicalTrials.gov registry record · NA

The Effect of Combined Spinal-Epidural Analgesia on the Success of External Cephalic Version (ECV) for Breech Position

A NA study, sponsored by Northwestern University.

Completed
Registry status
NA
Development phase
101
Enrollment target

NCT00565383 is a NA study that has completed, run by Northwestern University. The registered enrollment target is 101 participants.

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The verdict

NCT00565383, a NA study, has completed, sponsored by Northwestern University.

COMPLETED
Registry status
NA
Development phase
101 participants
Enrollment target

Study Summary

We aim to answer the clinical question: Does combined spinal-epidural analgesia improve the success rate of external cephalic version? We hypothesize that neuraxial analgesia (spinal or epidural analgesia) during version for breech presentation increases successful fetal rotation and decreases the incidence of Cesarean delivery for malpresentation.

Interventions

  • PROCEDURE Combined spinal-epidural analgesia
  • PROCEDURE Intravenous fentanyl (50mcg)

Trial Details

FieldValue
Enrollment Target 101 participants
Start Date 2002-08
Est. Completion 2006-06
Phase NA

Sponsor

Northwestern University

1,209 total trials

What the Registry Record Tells You About NCT00565383

The ClinicalTrials.gov registry entry for NCT00565383 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 101 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Northwestern University, which has 1,209 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Combined spinal-epidural analgesia is the first listed.

NCT00565383 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00565383 about?

NCT00565383 is a clinical study titled "The Effect of Combined Spinal-Epidural Analgesia on the Success of External Cephalic Version (ECV) for Breech Position". We aim to answer the clinical question: Does combined spinal-epidural analgesia improve the success rate of external cephalic version? We hypothesize that neuraxial analgesia (spinal or epidural analgesia) during version for breech presentation increases successful fetal rotation and decreases the i...

What is the current status of trial NCT00565383?

This trial is currently completed. It is a NA study. The enrollment target is 101 participants. The study started on 2002-08. Estimated completion is 2006-06.

What interventions are being tested in trial NCT00565383?

The interventions under investigation include: Combined spinal-epidural analgesia (PROCEDURE), Intravenous fentanyl (50mcg) (PROCEDURE).

Who is sponsoring clinical trial NCT00565383?

This trial is sponsored by Northwestern University, which has 1,209 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, or report a data error.