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NCT00638274 · ClinicalTrials.gov registry record · Phase 2

Comparison of Loss of Resistance Techniques

A Phase 2 study, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
Phase 2
Development phase
356
Enrollment target

NCT00638274 is a Phase 2 study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 356 participants.

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The verdict

NCT00638274, a Phase 2 study, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
Phase 2
Development phase
356 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether there is a difference in success outcome of the combined spinal epidural labor analgesia between air versus saline when used to identify the epidural space.

Interventions

  • PROCEDURE Air
  • PROCEDURE Saline

Trial Details

FieldValue
Enrollment Target 356 participants
Start Date 2005-07
Est. Completion 2008-05
Phase Phase 2

Sponsor

Wake Forest University Health Sciences

1,140 total trials

What the Registry Record Tells You About NCT00638274

The ClinicalTrials.gov registry entry for NCT00638274 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 356 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.

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

NCT00638274 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00638274 about?

NCT00638274 is a clinical study titled "Comparison of Loss of Resistance Techniques". The purpose of this study is to determine whether there is a difference in success outcome of the combined spinal epidural labor analgesia between air versus saline when used to identify the epidural space.

What is the current status of trial NCT00638274?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 356 participants. The study started on 2005-07. Estimated completion is 2008-05.

What interventions are being tested in trial NCT00638274?

The interventions under investigation include: Air (PROCEDURE), Saline (PROCEDURE).

Who is sponsoring clinical trial NCT00638274?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 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.