Kanuni SSRTH
Istanbul, 34303, Turkey (Türkiye)
NCT Number: NCT03701048
During Cesarean section in Group 1 rectus muscle will be closed with interrupted sutures. In group 2 rectus muscle will not be closed. Postoperative pain scores, distance between the rectus muscles and bowel functions will be evaluated.
Looking for future studies?
Notify Me18 year–40 year
Female
Interventional
Not applicable
Istanbul, 34303, Turkey (Türkiye)
Pfannenstiel incision will be done under general or spinal anesthesia. The abdomen will be opened and fetus and placenta will be delivered. Then the abdomen will be closed. In Group 1 rectus muscle will be closed with interrupted sutures. In group 2 rectus muscle will not be closed. Postoperative pain scores, distance between the rectus muscles and bowel functions will be evaluated.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Pfnannenstiel incision will be done under general or spinal anaesthesia. The abdomen will be opened and fetus and plasenta will be delivered. Then abdomen will be closed.
Time frame: 24 hours after the procedure
Visual Analog Scores, minimum score is 0, maximum score is 10. Score 10 represents highest pain score.
Time frame: 6 weeks after the procedure
Distance between the margins of the rectus muscles in centimeters will be measured with ultrasonography
Looking for future studies?
Notify MeKanuni Sultan Suleyman Training and Research Hospital
Other
Intraoperative and Postoperative Results of Rectus Musle Reapproximation During Cesarean Section
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06242756
Cesarean Section Complications
Calgary, Alberta, Canada
View Trial DetailsNCT06669156
Cesarean Section Complications, Cesarean Section Pain
Viborg, Region Midt, Denmark
View Trial DetailsNCT05840367
Cesarean Section Complications
Kolding, Denmark
View Trial DetailsNCT06970483
Cesarean Section Complications, Delivery Complication
Ankara, Turkey (Türkiye)
View Trial Details