Actively Recruiting
Niche Investigated: Closure of Hysterotomy & Evaluation of 3 Suturing Techniques (Running, Interrupted, and Locked)
Led by Cairo University · Updated on 2024-11-19
225
Participants Needed
5
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to explore the impact of three different suturing techniques (Running, Interrupted \& Locked) that used to close the uterine incision at the cesarean section on the formation of a cesarean scar niche
CONDITIONS
Official Title
Niche Investigated: Closure of Hysterotomy & Evaluation of 3 Suturing Techniques (Running, Interrupted, and Locked)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women with a singleton pregnancy scheduled for elective cesarean section
- Gestational age at cesarean section between 38 and 40 weeks
- Willingness to participate in the study and provide informed consent
- Age between 18 and 35 years old
- Body mass index (BMI) less than 30
You will not qualify if you...
- Known uterine anomalies or previous uterine surgery such as myomectomy or uterine septum resection
- Medical conditions that prevent cesarean delivery or affect uterine healing, including anemia and diabetes
- Current smokers
- Fetus in a non-cephalic (not head-down) position
- Low-lying anterior wall placenta or placenta previa
- Inability to provide informed consent due to cognitive issues or language barriers
- Any condition that poses a risk to the participant or study integrity, such as needing excessive suturing or uterine artery ligation
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 5 locations
1
Cairo University
Cairo, Egypt
Actively Recruiting
2
Cairo University
Cairo, Egypt
Actively Recruiting
3
Cairo University
Cairo, Egypt
Actively Recruiting
4
Cairo University
Cairo, Egypt
Actively Recruiting
5
Cairo University
Cairo, Egypt
Actively Recruiting
Research Team
A
Abdalla Moussa
CONTACT
S
Sally Collins
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
3
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