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NCT03261765 Clinical Trial

Effect of Multiple Repeat Cesarean Sections on Intra-abdominal Adhesions

Cesarean Section Complications Clinical Trial

Official title:
Effect of Multiple Repeat Cesarean Sections on Intra-abdominal Adhesions

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03261765
Other study ID # CSIAA
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 1, 2018
Est. completion date November 2018

Study information
Verified date June 2018
Source Assiut University
Contact Ahmed Abbas
Phone 01003385183
Email bmr90@hotmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The rate of cesarean section deliveries has increased dramatically worldwide in the last decades. While the cesarean birth rate was 4.5% in the USA in 1965, it was 31.8% according to 2007 data and is thought to be over 50% at present. The reasons for this include advanced age of primigravida, a wide range of indications, patient requests, the frequency of women with previous cesareans, women's rejections to offers of sterilization, and the common usage of assisted reproductive techniques

Recruitment information / eligibility
Status Recruiting
Enrollment 160
Est. completion date November 2018
Est. primary completion date August 2018
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

1. Women with at least previous one cesarean section.

2. Women accepted to participate in the study.

Exclusion Criteria:

1. Previous abdominopelvic surgery other than cesarean section.

2. History of Pelvic inflammatory disease.

3. Women refuse to participate in the study.

4. Intrauterine fetal death

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Assessment of adhesions
Modified Nair scoring system

Locations
Country Name City State
Egypt Ahmed Abbas Assiut Cairo

Sponsors (1)
Lead Sponsor Collaborator
Assiut University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Rate of abdominal adhesions 30 minutes
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