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Not listed Not applicable Interventional Accepts healthy volunteers

Skin Incisions and Wound Complication Rates for C-sections in Obese Women

ClinicalTrials.gov ID: NCT02685761

Public ClinicalTrials.gov record NCT02685761. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 18, 2026, 6:54 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Randomized Controlled Trial of Wound Complication Rates Between Low Transverse, Midline Vertical, and High Transverse Skin Incisions in Women With a BMI of 40 or Above Undergoing a Cesarean Section for Delivery

Brief summary

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

It is the purpose of this study to evaluate the relationship between a low transverse, vertical midline, and supra-panicular high transverse skin incisions and the rate of wound complications in women with a BMI of 40 or greater undergoing a cesarean section for delivery. So far, the choice of incision for the morbidly obese is based only on case reports. No randomized controlled trials have been done up to date comparing these methods. It is our hope that a high transverse incision will have all of the benefits of a low transverse skin incision, with the added benefit of better exposure offered by a vertical midline incision, without the added increased risk of subjecting the woman to a vertical hysterotomy.

Study identification

NCT ID
NCT02685761
Recruitment status
Not listed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Albany Medical College
Other
Enrollment
309 participants

Conditions and interventions

Eligibility (public fields only)

Age range
Not listed
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
Aug 31, 2015
Primary completion
Aug 31, 2020
Completion
Aug 31, 2021
Last update posted
Sep 12, 2016

2015 – 2021

United States locations

U.S. sites
6
U.S. states
1
U.S. cities
5
Facility City State ZIP Site status
Albany Medical Center Obstetrics and Gynecology Albany New York 12208 Recruiting
Albany Medical Center Albany New York 12208 Recruiting
Albany Medical Center Obstetrics and Gynecology Ballston Spa New York 12020 Recruiting
Albany Medical Center Obstetrics and Gynecology Clifton Park New York 12065 Recruiting
Albany Medical Center Obstetrics and Gynecology Delmar New York 12054 Recruiting
Albany Medical Center Obstetrics and Gynecology Latham New York 12110 Recruiting

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 NCT02685761, 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 Sep 12, 2016 · Synced Sep 18, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02685761 live on ClinicalTrials.gov.

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