Sharp Versus Blunt Fascial Incision at Caesarean Section

Status Completed

Clinical Trial Summary

The purpose of this study is to compare sharp and blunt fascial entry during caesarean section on the same patient. The study is performed on woman having cesarean section for the first time and who have not previously had lower abdominal surgery done. The following parameters are registered:

1. The preferred side evaluated by the patient 3 months postoperatively.

2. The patient evaluated difference in pain on the right vs. left side 1, 3 and 7 days and 1 and 3 months postoperatively.

3. The rate and side of infection.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Cesarean Section

Clinical Trial Details

NCT number	NCT01297725
Study type	Interventional
Source	Holbaek Sygehus
Contact
Status	Completed
Phase	N/A
Start date	January 2011
Completion date	October 2011

View Details

See also
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