Skin Adhesive Plus Intra-cuticular Suture Versus Suture Alone for Cesarean Skin Closure
Recruiting
N/A
Interventional Study
Surgical Site Infection (SSI)
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 240 (estimated)
- Sponsor
- Doron Kabiri · Other
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About This Trial
The goal of this randomized control trial is to compare two skin closure techniques after cesarean section. Both techniques are currently in wide use but no comparison between the two was reasserted yet. The two techniques are- First technique is intracuticular suture using monofilament suture, Second technique is intracuticular suture and biological adhesive material. The investigators' primary o…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients undergoing elective cesarean section at Hadassa medical center
* Patients undergoing elective cesarean section btween 37+0/7 and 41+6/7 weeks of gestation
Exclusion Criteria:
* Patients undergoing emergency cesarean section
* patients undergoing cesarean section bef…
Contacts