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NCT00727025 · ClinicalTrials.gov registry record · NA

Randomized Controlled Trial of Subcuticular Skin Closure Versus Steri-strip S Closure

A NA study, sponsored by Dartmouth-Hitchcock Medical Center.

Completed
Registry status
NA
Development phase
51
Enrollment target

NCT00727025 is a NA study that has completed, run by Dartmouth-Hitchcock Medical Center. The registered enrollment target is 51 participants.

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The verdict

NCT00727025, a NA study, has completed, sponsored by Dartmouth-Hitchcock Medical Center.

COMPLETED
Registry status
NA
Development phase
51 participants
Enrollment target

Study Summary

Purpose: The aims of this randomized clinical trial are: 1. to assess scar quality from the patient and surgeon perspectives 2. to assess patient comfort in the days immediately following surgery 3. to assess the time taken to complete closure in the operating room. 4. the financial benefit or cost for the institution of using Steri Strip S will also be estimated. Two closure methods will be compared, a new coaptive film device (Steri Strip S) versus standard subcuticular sutures. The linear incisions will include the standard incision segments utilized for an inverted-T closure for bilateral breast reduction and the transabdominal incision segments utilized for abdominoplasty or TRAM flap harvest. Our hypothesis is that incisions segments closed with Steri Strip S compared to standard subcuticular closure, will yield scars of better cosmetic quality, in shorter time to closure, with novice and expert surgeons, for both bilateral breast reduction and abdominoplasty surgical procedures.

Interventions

  • DEVICE wound closure device (Steri-Strip™)

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2005-07
Est. Completion 2008-03
Phase NA

Sponsor

Dartmouth-Hitchcock Medical Center

427 total trials

What the Registry Record Tells You About NCT00727025

The ClinicalTrials.gov registry entry for NCT00727025 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 51 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Dartmouth-Hitchcock Medical Center, which has 427 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which wound closure device (Steri-Strip™) is the first listed.

NCT00727025 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00727025 about?

NCT00727025 is a clinical study titled "Randomized Controlled Trial of Subcuticular Skin Closure Versus Steri-strip S Closure". Purpose: The aims of this randomized clinical trial are: 1. to assess scar quality from the patient and surgeon perspectives 2. to assess patient comfort in the days immediately following surgery 3. to assess the time taken to complete closure in the operating room. 4. the financial benefit or cost...

What is the current status of trial NCT00727025?

This trial is currently completed. It is a NA study. The enrollment target is 51 participants. The study started on 2005-07. Estimated completion is 2008-03.

What interventions are being tested in trial NCT00727025?

The interventions under investigation include: wound closure device (Steri-Strip™) (DEVICE).

Who is sponsoring clinical trial NCT00727025?

This trial is sponsored by Dartmouth-Hitchcock Medical Center, which has 427 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.