Clinical trials: Cesarean Resection
Wound Disruption, Wound Infection
Early Bandage Removal Post-Cesarean Delivery
Women undergoing their first second or third cesarean section will be randomized into two groups. One group will have the abdominal bandage removed at 6 hours post-surgery and the other group will have the bandage removed at 24…
- Trial name
- NCT01867567
- Testing
- abdominal bandage
- Where
- Israel
- Volunteers
- 320 people
- Sponsor
- Ziv Hospital
Cesarean Section; Wound, Infection (Following Delivery)
Removal of Surgical Staples After Cesarean Delivery. Randomized Control Trial.
The optimal choice of skin closure at cesarean delivery has not yet been determined. This study aim to study the wound complications and scar healing after Surgical staples removal at postoperative day 4 and day 8 .
- Trial name
- ROCD (NCT03063853)
- Testing
- Removal of surgical clips at day 4 post operative vs day 8 post operative, Elective cesarean delivery
- Where
- Israel
- Volunteers
- 104 people, healthy volunteers welcome
- Sponsor
- Wolfson Medical Center
Surgical Site Infection
The Effect of Timing of Removal of Wound Dressing on Surgical Site Infection Rate After Cesarean Delivery
A randomized controlled trial measuring surgical site infection rate as a function of timing of wound dressing removal.
- Trial name
- NCT02902419
- Testing
- Wound dressing removal.
- Where
- 2 sites in United States
- Volunteers
- 602 people
- Sponsor
- Albany Medical College
Quality of Life, Sexual Activity
Quality of Life and Sexual Function of Vaginal Operation in The Treatment Of Previous Cesarean Scar Defect
The aim of this study is to further demonstrate the safety , validity and quality of (sexual)life of vaginal operation for previous cesarean scar defect resection.
- Trial name
- PCSD (NCT01978067)
- Testing
- transvaginal resection of Uterine Scar
- Where
- China
- Volunteers
- 60 people
- Sponsor
- Shu-Qin Chen
Pregnancy, Labor; Forced or Induced, Affecting Fetus or Newborn
Outpatient Labor Induction With the Transcervical Foley Balloon
This study represents the first randomized trial comparing traditional inpatient induction with a transcervical foley catheter versus outpatient induction with immediate removal of a transcervical foley catheter.
- Trial name
- NCT02210598
- Testing
- inpatient Foley balloon induction, outpatient Foley balloon induction, Oxytocin
- Where
- United States
- Volunteers
- 64 people
- Sponsor
- University of Southern California
Cesarean Section Complications, Scar Niche
Uterine Scar Resection During Repeat Cesarean Delivery to Prevent Uterine Niche Formation
The purpose of the study is to evaluate whether resection of the previous cesarean scar at repeat cesarean delivery reduces uterine niche formation and related morbidity without increasing operative risks.
- Conditions
- Cesarean Section Complications, Scar Niche, Scarred Uterus
- Trial name
- NCT07228858
- Testing
- Repeated cesarean section with previous uterine cesarean section scar resection, Repeated cesarean section without uterine scar resection, Saline-infusion Sonohysterography
- Where
- Egypt
- Volunteers
- 170 people
- Sponsor
- Benha University
Postpartum Hemorrhage, Cesarean Section Complications
Placental Removal Method And Uterine Massage On Preventing Postpartum Hemorrhage
Postpartum hemorrhage is the leading cause of maternal deaths in all over the world, especially in developing and underdeveloped countries. Medical and surgical methods exist for management of bleeding.
- Conditions
- Postpartum Hemorrhage, Cesarean Section Complications, Uterine Atony
- Trial name
- NCT06192836
- Testing
- Manual Removal 1, Manual Removal 2, Controlled Cord Traction 1
- Where
- Turkey (Türkiye)
- Volunteers
- 361 people
- Sponsor
- Busra Lekesiz
Scar Niche, Abnormal Uterine Bleeding
Sublingual Misoprostol Versus No Cervical Priming Before Hysteroscopic Resection of Symptomatic Uterine Niches
The purpose of the study is to evaluated whether preoperative sublingual misoprostol can enhance the effectiveness and safety of niche resection in patients with symptomatic uterine niche.
- Conditions
- Scar Niche, Abnormal Uterine Bleeding, Cesarean Section Complications
- Trial name
- NCT07271056
- Testing
- Misoprostol 200mcg Tab, Hysteroscopic resection of uterine niche, Saline-infusion Sonohysterography
- Where
- Egypt
- Volunteers
- 56 people
- Sponsor
- Benha University
Wound Complications, Obesity
Early Versus Delayed Skin Staple Removal Following Cesarean Delivery in the Obese Patient
Whenever a person has a cesarean section there is a risk that there will be a problem with healing of the wound. The most common type of wound healing problem is separation and opening of the skin and fatty tissue just beneath…
- Trial name
- NCT01114451
- Testing
- Removal of surgical skin staples
- Where
- United States
- Volunteers
- 292 people, healthy volunteers welcome
- Sponsor
- Prisma Health-Upstate