- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03261765
Effect of Multiple Repeat Cesarean Sections on Intra-abdominal Adhesions
June 26, 2018 updated by: Ahmed Mohamed Abbas, Assiut University
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
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
160
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Cairo
-
Assiut, Cairo, Egypt, 002
- Recruiting
- Ahmed Abbas
-
Contact:
- ahmed abbas
- Email: bmr90@hotmail.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 50 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Sampling Method
Probability Sample
Study Population
All women with repeated cesarean section
Description
Inclusion Criteria:
- Women with at least previous one cesarean section.
- Women accepted to participate in the study.
Exclusion Criteria:
- Previous abdominopelvic surgery other than cesarean section.
- History of Pelvic inflammatory disease.
- Women refuse to participate in the study.
- Intrauterine fetal death
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Multiple repeat cesarean (four or more)
|
Modified Nair scoring system
|
Fewer repeat cesarean (two-three)
|
Modified Nair scoring system
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Rate of abdominal adhesions
Time Frame: 30 minutes
|
30 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
June 1, 2018
Primary Completion (Anticipated)
August 1, 2018
Study Completion (Anticipated)
November 1, 2018
Study Registration Dates
First Submitted
August 23, 2017
First Submitted That Met QC Criteria
August 23, 2017
First Posted (Actual)
August 25, 2017
Study Record Updates
Last Update Posted (Actual)
June 27, 2018
Last Update Submitted That Met QC Criteria
June 26, 2018
Last Verified
June 1, 2018
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CSIAA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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