Dermabond Skin Adhesives vs Skin Staples for Closure of Repeat Cesarean Section Skin Incisions

ClinicalTrials.gov ID: NCT00505856

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Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The use of dermabond skin adhesive vs. skin staples for the closure of repeat c-section incisions.

Study identification

NCT ID: NCT00505856
Recruitment status: Terminated
Study type: Observational
Phase: Not listed
Lead sponsor: Texas Tech University Health Sciences Center; Other
Enrollment: 50 participants

Conditions and interventions

Conditions

Pregnancy

Interventions

Not listed

Eligibility (public fields only)

Age range: 18 Years to 50 Years
Sex: Female
Healthy volunteers: Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date: Jul 2007 (Type not available)
Primary completion: Not listed
Completion: Dec 2007 (Actual)
Last update posted: Dec 12, 2008

2007

United States locations

U.S. sites: 1
U.S. states: 1
U.S. cities: 1

Facility	City	State	ZIP	Site status
Texas Tech University HSC Dept OB/GYN	Lubbock	Texas	79403	—

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows: Public field values for ClinicalTrials.gov record NCT00505856, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do: No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from: Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh: Last update posted Dec 12, 2008 · Synced Nov 15, 2026