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Clinical Trial Summary

In this study the investigators want to asses the effect of peritonisation at c-section on postoperative vital signs which was thought to be an indirect finding secondary to increased sympathetic activity originated from pain caused by stretched peritoneum.


Clinical Trial Description

At c-section subject will be randomised into four groups:

Group1: Only visceral peritoneum will be closed

Group 2: Only parietal peritoneum will be closed

Group 3: Both of them will be closed

Group 4: None of them will be closed

During the postoperative period all patients will undergo vital sign screening including urine output, blood pressure measurement, pulse rate and VAS score will be determined at post operative 6th hour and 24th hour. ;


Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Screening


Related Conditions & MeSH terms


NCT number NCT02581293
Study type Interventional
Source Zeynep Kamil Maternity and Pediatric Research and Training Hospital
Contact Meryem Kurek EKEN, MD
Phone +905305104468
Email meryemkurek@yahoo.com
Status Recruiting
Phase Phase 1
Start date March 2015
Completion date February 2016

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