CompletedNot Applicable

Comparison of Staples Versus Subcuticular Suture in Class III Obese Women Undergoing Cesarean Delivery

United States238 participantsStarted 2015-06

Plain-language summary

The purpose of this study is to determine the optimal skin closure technique (staples versus subcuticular suture) at the time of cesarean delivery in Class III obese women with body mass index (BMI) of \>/= 40kg/m2.

Who can participate

Age range

18 Years – 65 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Women \> 18 years old undergoing cesarean delivery (CD)
. BMI of \>/= 40 kg/m2 as determined by height and weight reported during their admission
. Live gestation 23 weeks or greater
. Women who are able to follow-up 7-14 days after hospital discharge for a visual wound check.

Exclusion criteria

. Active lupus flare
. HIV/AIDS
. Current treatment for cancer or h/o radiation to the abdomen/pelvis
. Hypersensitivity to steri-strips

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Composite Wound Complication at Hospital Discharge and 2 Weeks Postpartum

Timeframe: At hospital discharge, at 2 weeks postpartum and at 6 weeks postpartum

Trial details

NCT IDNCT02466776

SponsorMemorialCare Health System

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2015-10

Results submitted2023-01-18

View on ClinicalTrials.gov More Obesity, Severe trials