- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06788899
Clinical Audit on Uterine Closure During Caesarean Section in Assiut Women's Health Hospital
January 17, 2025 updated by: Lobna Hassan Ahmed AbdelRhman, Assiut University
Auditing of closure of uterine incision in Caesarean section in Assiut Women's Health Hospital.
Study Overview
Status
Not yet recruiting
Conditions
Study Type
Observational
Enrollment (Estimated)
300
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Lobna Hassan AbdelRhman, Graduate
- Phone Number: 0201146398546
- Email: hassanlobna368@gmail.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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
All elective Caeserean sections with no medical or obestetric disorder
Description
Inclusion Criteria:
- all elective Caesarean section
Exclusion Criteria:
- Placenta previa
- Chorioamionitis
- PROM
- Diabetic women
- Immunocompromised women
- Women with heart disease
- Women with renal or liver disease
- Women on corticosteroids therapy
- Preeclampsia
- Women with hypertensive disorders
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Improve performance of closure of Caesarean section. in Assiut Women health hospital according to NICE guidelines and National Library of Medicine
Time Frame: Through study completion an average of one year
|
Questionaire
|
Through study completion an average of one year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Decrease complications of caeserean section
Time Frame: Through study completion an average of one year
|
Questionaire
|
Through study completion an average of one year
|
|
Training of university staff
Time Frame: Through study completion an average of one year
|
Questionaire
|
Through study completion an average of one year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Principles of Methodological Design of Clinical Audit. Arch Med Vol No:10 Iss No:2:2(1)
- 1-Morrell C and Harvey G (1999) The Clinical Audit Handbook. Improving the quality of health care. London: Bailliere Tindall.(1)
- Hauth JC, Owen J, Davis RO. Transverse uterine incision closure: one versus two layers. Am J Obstet Gynecol. 1992 Oct;167(4 Pt 1):1108-11. doi: 10.1016/s0002-9378(12)80048-2.
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 (Estimated)
January 1, 2025
Primary Completion (Estimated)
January 1, 2026
Study Completion (Estimated)
May 1, 2026
Study Registration Dates
First Submitted
December 22, 2024
First Submitted That Met QC Criteria
January 17, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
January 17, 2025
Last Verified
December 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- Uterus closure
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
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.
Clinical Trials on Uterine Closure in Caesarean Section
-
University Hospital, GhentTerminatedCaesarean Section | Learning Curve | Intra-uterine DeviceBelgium
-
Ankara City Hospital BilkentRecruitingCaesarean Section | Clinical Outcomes | Myometrial Thickness | Cesarean Scar Closure | Cesarean Scar Defect (Isthmococele) | Postpartum ComplicationsTurkey (Türkiye)
-
Ashulia Women and Children HospitalCompleted
-
Assiut UniversityCompletedCaesarean SectionEgypt
-
Taipei Medical University WanFang HospitalCompletedCaesarean SectionTaiwan
-
South Tees Hospitals NHS Foundation TrustCompletedCaesarean Section | Caesarean Section; InfectionUnited Kingdom
-
Sichuan Provincial People's HospitalNot yet recruiting
-
Shanghai First Maternity and Infant HospitalUnknownCaesarean SectionChina
-
Karamanoğlu Mehmetbey UniversityRecruitingCaesarean SectionTurkey (Türkiye)