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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02679365
Other study ID # 2476ASU
Secondary ID
Status Completed
Phase N/A
First received February 7, 2016
Last updated July 30, 2017
Start date March 2016
Est. completion date July 2017

Study information

Verified date July 2017
Source Ain Shams Maternity Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this trial we compare the effect of 2 closure techniques of the rectus sheath during cesarean sections on postoperative pain. One closure technique is double lock technique and the other is the conventional continuous non-locking technique.


Recruitment information / eligibility

Status Completed
Enrollment 150
Est. completion date July 2017
Est. primary completion date July 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria:

- first cesarean section

Exclusion Criteria:

- urgent cesarean section

- previous abdominal surgery

- previous cesarean section

- obstetric and medical complications

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
lower segment cesarean section and double lock closure of rectus sheath

lower segment cesarean section and continuous non-locking closure of rectus sheath


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams Maternity Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary postoperative pain evaluated by VAS first week postoperative
Secondary operative time intraoperative
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