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NCT00654641 · ClinicalTrials.gov registry record · NA

Prevention of Wound Complications After Cesarean Delivery in Obese Women Utilizing Negative Pressure Wound Therapy

A NA study, sponsored by West Virginia University.

Terminated
Registry status
NA
Development phase
54
Enrollment target

NCT00654641 is a NA study that was terminated before completion, run by West Virginia University. The registered enrollment target is 54 participants.

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The verdict

NCT00654641, a NA study, was terminated before completion, sponsored by West Virginia University.

TERMINATED
Registry status
NA
Development phase
54 participants
Enrollment target

Study Summary

Wound complications after Cesarean section (C-section) are common in obese women. Approximately 25% of obese women having a C-section will have a wound complication. This research study is designed to assess whether applying a source of vacuum (suction) to the wound can reduce the risk of wound complications. The investigators plan to enroll 220 women into the study. Women will be randomly selected to receive standard stitching and stapling of the incision (cut on the abdomen) or closure with stitches, staples and wound suction. Subjects will be seen for follow-up visits in 7-14 days and again at 4-6 weeks after surgery. The number of wound complications in each group will be compared. If the wound suction technique is successful in preventing wound complications, this may substantially reduce pain and suffering in a large number of women undergoing C-section for delivery.

Interventions

  • PROCEDURE Negative pressure wound closure
  • PROCEDURE Standard wound closure

Trial Details

FieldValue
Enrollment Target 54 participants
Start Date 2007-09
Est. Completion 2010-02
Phase NA

Sponsor

West Virginia University

122 total trials

What the Registry Record Tells You About NCT00654641

The ClinicalTrials.gov registry entry for NCT00654641 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 54 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is West Virginia University, which has 122 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Negative pressure wound closure is the first listed.

NCT00654641 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00654641 about?

NCT00654641 is a clinical study titled "Prevention of Wound Complications After Cesarean Delivery in Obese Women Utilizing Negative Pressure Wound Therapy". Wound complications after Cesarean section (C-section) are common in obese women. Approximately 25% of obese women having a C-section will have a wound complication. This research study is designed to assess whether applying a source of vacuum (suction) to the wound can reduce the risk of wound comp...

What is the current status of trial NCT00654641?

This trial is currently terminated. It is a NA study. The enrollment target is 54 participants. The study started on 2007-09. Estimated completion is 2010-02.

What interventions are being tested in trial NCT00654641?

The interventions under investigation include: Negative pressure wound closure (PROCEDURE), Standard wound closure (PROCEDURE).

Who is sponsoring clinical trial NCT00654641?

This trial is sponsored by West Virginia University, which has 122 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.