Clinical Trials Directory

Trials / Completed

CompletedNCT04220294

Subcutaneous Continuous Versus Interrupted Sutures During Cesarean Section.

Surgical Site Infection Rate After Subcutaneous Continuous Versus Interrupted Sutures During Cesarean Section.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
1,238 (actual)
Sponsor
Rambam Health Care Campus · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

A comparison of the rate of surgical site infections after cesarean section depending on the type of suture used for subcutaneous closure-continuous versus interrupted.

Detailed description

Patients at term that are candidates for elective cesarean section will receive an explanation regarding the study and sign informed consent. Patients will then be divided randomly to one of 2 treatment groups based on the type of subcutaneous tissue closure: 1. Interrupted sutures. 2. Continuous sutures. Information regarding medical and obstetric history will be collected for each patient.

Conditions

Interventions

TypeNameDescription
PROCEDURESubcutaneous tissue closureSubcutaneous tissue closure with 2-0 vicryl suture.

Timeline

Start date
2020-01-10
Primary completion
2022-04-30
Completion
2022-10-20
First posted
2020-01-07
Last updated
2023-02-21

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT04220294. Inclusion in this directory is not an endorsement.