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NCT03184077 · ClinicalTrials.gov registry record · NA

Rapidly Absorbing Polyglactin 910 Versus Poliglecaprone 25 for Laceration Repair

A NA study, sponsored by Virginia Commonwealth University.

Completed
Registry status
NA
Development phase
318
Enrollment target

NCT03184077 is a NA study that has completed, run by Virginia Commonwealth University. The registered enrollment target is 318 participants.

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The verdict

NCT03184077, a NA study, has completed, sponsored by Virginia Commonwealth University.

COMPLETED
Registry status
NA
Development phase
318 participants
Enrollment target

Study Summary

To evaluate the rates of dyspareunia with rapidly absorbing polyglactin 910 compared to poliglecaprone 25 using a validated sexual function questionnaire. To assess maternal satisfaction with the laceration repair and suture material. To assess overall perineal pain using a visual analog scale. To assess the rate of wound breakdown and the need for suture removal.

Interventions

  • PROCEDURE Laceration Repair with Polyglactin 910
  • PROCEDURE Laceration Repair with poliglecaprone 25

Trial Details

FieldValue
Enrollment Target 318 participants
Start Date 2014-09-02
Est. Completion 2017-08-27
Phase NA

Sponsor

Virginia Commonwealth University

558 total trials

What the Registry Record Tells You About NCT03184077

The ClinicalTrials.gov registry entry for NCT03184077 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 318 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Virginia Commonwealth University, which has 558 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Laceration Repair with Polyglactin 910 is the first listed.

NCT03184077 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT03184077 about?

NCT03184077 is a clinical study titled "Rapidly Absorbing Polyglactin 910 Versus Poliglecaprone 25 for Laceration Repair". To evaluate the rates of dyspareunia with rapidly absorbing polyglactin 910 compared to poliglecaprone 25 using a validated sexual function questionnaire. To assess maternal satisfaction with the laceration repair and suture material. To assess overall perineal pain using a visual analog scale. T...

What is the current status of trial NCT03184077?

This trial is currently completed. It is a NA study. The enrollment target is 318 participants. The study started on 2014-09-02. Estimated completion is 2017-08-27.

What interventions are being tested in trial NCT03184077?

The interventions under investigation include: Laceration Repair with Polyglactin 910 (PROCEDURE), Laceration Repair with poliglecaprone 25 (PROCEDURE).

Who is sponsoring clinical trial NCT03184077?

This trial is sponsored by Virginia Commonwealth University, which has 558 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.