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Clinical Trial 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.


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04220294
Study type Interventional
Source Rambam Health Care Campus
Contact
Status Completed
Phase N/A
Start date January 10, 2020
Completion date October 20, 2022

See also
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