Clinical Trials Logo

Clinical Trial Summary

The first group patients underwent double layer closure with split thickness with vicryl 2/0, in continuous, non- locked, 1 cm apart sutures, study group, and the second group, women underwent double layer closure with split thickness with vicryl 1, in continuous, non- locked, 1 cm apart sutures, control group. Then, all women in the study were followed up for development of niche within 1 to 6 weeks. The assessment after one week postpartum was with using trans-abdominal Ultrasound, then after two to six weeks postpartum with transvaginal Ultrasound


Clinical Trial Description

Caesarean section rates have increased worldwide over the past decades from 6.7 to 19.1%, with a current European CS rate of 25% of all births. CS is considered to be a safe procedure that can be life saving for both mother and child but the increasing trend draws more attention to adverse outcomes related to CSs. A relatively new long-term sequela is the niche in the uterine caesarean scar. A niche is defined as "an indentation at the site of the uterine caesarean scar with a depth of at least 2 mm on ultrasound" and is present in 56-84% of women after one or more CSs . It is realized that almost all of the increase in cesarean section rate is due to the increase in repeat operations, and primary cesarean deliveries for dystocia and fetal distress. These can be attributed to obstetric factors as increased primary cesarean delivery rate, failed induction. Maternal factors as Increased proportion of women > age 35, increased nulliparous women, increased elective primary cesarean deliveries and factors relating to the physician as Malpractice litigation concerns . The hypotheses can be divided into surgery-related factors and patient related factors. In their paper they focused on surgery-related factors since these could be easily modified and studied in future RCTs . These surgical-related factors include low (cervical) location of the uterine incision during a CS, Incomplete closure of the uterine wall, due to single-layer, endometrial saving closure technique or use of locking sutures and Surgical activities that may induce adhesion formation (i.e., non-closure of peritoneum, inadequate hemostasis, applied sutures, use of adhesion barriers). Without questions, the uterine niche presents a pathology that requires evaluation and intervention to mitigate its prevalence. The aim of this study is to compare between closures of uterine incision with Vicryl 2/0 versus Vicryl 1 in developing a uterine niche. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05770115
Study type Interventional
Source Cairo University
Contact
Status Completed
Phase N/A
Start date November 1, 2020
Completion date February 10, 2023

See also
  Status Clinical Trial Phase
Completed NCT01890720 - Incisional Negative Pressure Wound Therapy for Prevention of Postoperative Infections Following Caesarean Section N/A
Completed NCT04076904 - Cesarean Niche Examination by Transvaginal us
Completed NCT05948150 - The Effect of Breastfeeding Pillow on Breastfeeding Self-Efficacy and Postpartum Comfort in Women Who Had Cesarean N/A
Completed NCT02369133 - Preemptive Analgesia With Intravenous Paracetamol for Post-cesarean Section Pain Control Phase 4
Completed NCT01891006 - Intervention for Postpartum Infections Following Caesarean Section N/A
Recruiting NCT05206682 - Comparison of the Therapeutic Effects of Vaginal Repair With Leuprorelin and Vaginal Repair in the Treatment of Cesarean Section Scar Defect N/A
Completed NCT03498339 - The Effect of Cesarean Operative Technique on the Occurrence of Large Hysterotomy Scar Defects N/A
Recruiting NCT05590104 - Hysteroscopic Isthmocele Repair on IVF Outcome N/A
Completed NCT04046783 - Patch With Onion Extract and Allantoin for C-section Scar
Withdrawn NCT05363735 - Ultrasound Elastography Application in Cesarean Section Scar Defect
Recruiting NCT03936309 - A Comparison of Scar Infiltration, Scar Deactivation, and Standard of Care for the Treatment of Chronic, Post-Surgical Pain After Cesarean Section N/A
Recruiting NCT03140683 - Predictors of Scar Dehiscence in Patients With Previous Caesarean Section
Completed NCT03257514 - Effect of Alpha Lipoic Acid on Uterine Scar Healing After Cesarean Section Phase 2
Completed NCT03859258 - Ultrasound Based Study For Niche Development In The Uterine Cesarean Section Scar
Recruiting NCT03829774 - To Study and Evaluate the Effectiveness of Treatment by Percutaneous Electrical NeuroStimulation (PENS) for Post-operative Pain in Cesarean Section Patients Using Primary Relief v 2.0 N/A
Completed NCT06256822 - Technology-Based Breastfeeding Training After Cesarean
Completed NCT04070118 - Lower Uterine Segment Thickness and Term Pain,Previous Cesarean Section
Completed NCT03130387 - Prevalence of Cesarean Section Niche in Women With Unexplained Abnormal Uterine Bleeding N/A
Recruiting NCT03471858 - Mechanical Dilation of the Cervix in a Scarred Uterus N/A
Recruiting NCT05536869 - Study Comparing a Cohort of Women Having a Classic Caesarean to a Cohort of Women Having a FAUCS Caesarean (FAUCS) N/A