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NCT03887299 · ClinicalTrials.gov registry record · Phase 4

Antimicrobial Dressing Versus Standard Dressing in Obese Women Undergoing Cesarean Delivery

A Phase 4 study, sponsored by The University of Texas Medical Branch, Galveston.

Completed
Registry status
Phase 4
Development phase
154
Enrollment target

NCT03887299 is a Phase 4 study that has completed, run by The University of Texas Medical Branch, Galveston. The registered enrollment target is 154 participants.

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The verdict

NCT03887299, a Phase 4 study, has completed, sponsored by The University of Texas Medical Branch, Galveston.

COMPLETED
Registry status
Phase 4
Development phase
154 participants
Enrollment target

Study Summary

This will be an open label pilot randomized controlled clinical trial. Women undergoing cesarean delivery will be randomized to have standard wound dressing care or chlorohexidine gluconate (CHG) impregnated wound dressing (ReliaTect™ Post-Op Dressing).

Interventions

  • COMBINATION_PRODUCT ReliaTect™ Post-Op Dressing (contains chlorohexidine gluconate or CHG)
  • OTHER Standard Wound Care

Trial Details

FieldValue
Enrollment Target 154 participants
Start Date 2019-04-18
Est. Completion 2020-02-28
Phase Phase 4

What the Registry Record Tells You About NCT03887299

The ClinicalTrials.gov registry entry for NCT03887299 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 154 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Medical Branch, Galveston, which has 203 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which ReliaTect™ Post-Op Dressing (contains chlorohexidine gluconate or CHG) is the first listed.

NCT03887299 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03887299 about?

NCT03887299 is a clinical study titled "Antimicrobial Dressing Versus Standard Dressing in Obese Women Undergoing Cesarean Delivery". This will be an open label pilot randomized controlled clinical trial. Women undergoing cesarean delivery will be randomized to have standard wound dressing care or chlorohexidine gluconate (CHG) impregnated wound dressing (ReliaTect™ Post-Op Dressing).

What is the current status of trial NCT03887299?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 154 participants. The study started on 2019-04-18. Estimated completion is 2020-02-28.

What interventions are being tested in trial NCT03887299?

The interventions under investigation include: ReliaTect™ Post-Op Dressing (contains chlorohexidine gluconate or CHG) (COMBINATION_PRODUCT), Standard Wound Care (OTHER).

Who is sponsoring clinical trial NCT03887299?

This trial is sponsored by The University of Texas Medical Branch, Galveston, which has 203 total clinical trials registered on ClinicalTrials.gov.

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

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