Actively Recruiting
Subcutaneous Lavage in Cesarean Section
Led by Hadassah Medical Organization · Updated on 2025-03-19
600
Participants Needed
1
Research Sites
218 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn if antiseptic washing prior to skin closure during cesarean section reduces rates of surgical site infection. intraoperative washing is a common practice in other surgical fields and several studies have shown efficacy in reducing postoperative infection rates. no randomized control trial has tested this intervention during cesarean section. The main questions we aim to answer are: Does subcutaneous antiseptic washing reduce the rates of surgical site infection? Does antiseptic washing improve scar healing? Does antiseptic washing reduce hospital stay, postpartum fever rates and readmission cases? Researchers will compare subcutaneous antiseptic washing to no intervention to see if surgical site infection rates reduce Participants will: consent to participate in the trial Visit the postpartum clinic 30 days after surgery
CONDITIONS
Official Title
Subcutaneous Lavage in Cesarean Section
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant women undergoing cesarean delivery
You will not qualify if you...
- Pregnant women undergoing vaginal delivery
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Hadassah Medical Organization
Jerusalem, Israel
Actively Recruiting
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
2
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