Clinical trials: Cesarean
Abnormal Uterine Bleeding, Cesarean Section Complications
Oral Contraceptive Pills Versus Levonorgestrel-Releasing Intrauterine System for Niche-Related Abnormal Uterine Bleeding
The purpose of the study is to compare the clinical efficacy and niche morphological changes following treatment with combined oral contraceptive pills (OCPs) versus a levonorgestrel-releasing intrauterine system (LNG-IUS) in…
- Conditions
- Abnormal Uterine Bleeding, Cesarean Section Complications, Uterine Scar
- Trial name
- NCT07229209
- Testing
- transvaginal ultrasonography, monophasic combined oral contraceptive pill, 52 mg levonorgestrel-releasing intrauterine system
- Where
- Egypt
- Volunteers
- 166 people
- Sponsor
- Benha University
Infertility Due to Nonimplantation, Infertility Secondary
Inflammation Markers in Fluid Aspirate From a Scarred Uterine vs. a Normal Uterine Cavity
A prospective study that will take place in the hydrosonography clinic, comparing patients with an intact uterus to those who had a caesarean section.
- Conditions
- Infertility Due to Nonimplantation, Infertility Secondary, Cesarean Section Complications
- Trial name
- NCT06322498
- Testing
- Uterine lavage
- Where
- Israel
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Hadassah Medical Organization
Cesarean Section, Complication
A Skin Glue Versus Subcuticular Suture for Cesarean Closure Study
The aim of this study is to compare cesarean incision outcomes between patients with incision closed with the Dermabond Prineo system compared to standard subcuticular suture.
- Conditions
- Cesarean Section, Complication, Wound
- Trial name
- NCT05903547
- Testing
- Dermabond Prineo, Suture
- Where
- United States
- Volunteers
- 151 people
- Sponsor
- Columbia University
Light Color Temperature
Effect of Reduced Light Color Temperature on Postpartum Mothers' Well-being, Breastfeeding Motivation, and Psychological Well-being After Cesarean Section
The aim of this study is to determine the effects of reduced light color temperature on postpartum mothers' well-being, breastfeeding motivation, and psychological well-being after cesarean section.
- Trial name
- NCT07104045
- Testing
- Reduced light color temperature
- Volunteers
- 80 people, healthy volunteers welcome
- Sponsor
- Emine Yıldırım
Anesthesia, Spinal
Intrathecal Dexmedetomidine With Bupivacaine for Spinal Anesthesia in Cesarean Section
A Randomized, Controlled, Double blind study aiming to evaluate the analgesic potentials and side effect profile of different dose levels of Dexmedetomidine added to subarachnoid bupivacaine in full-term pregnant women undergoing…
- Trial name
- NCT02365857
- Testing
- Dexmedetomidine & Bupivacaine., Bupivacaine Only.
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Cairo University
Cesarean Section, Obesity
Comparison of Tissue Retractors During Cesarean Delivery in Obese Women
This is a randomized controlled trial comparing the use of the Mobius™ retractor to the use of traditional metal retraction instruments in non-urgent cesarean deliveries of obese women.
- Trial name
- NCT00358592
- Testing
- Mobius™ retractor, traditional metal retraction instruments
- Where
- United States
- Volunteers
- 60 people
- Sponsor
- Thomas Jefferson University
Cesarean Section Complications, Hypothermia
The Effect of Forced Air Warming During Caseraen Section on Maternal Hypothermia: Randomized Controlled Trial
During the cesarean section; Hypothermia can be seen due to reasons such as anesthesia, premedication drugs, cold operating room environment, exposure of tissues and organs, and use of cold intravenous fluids.
- Trial name
- NCT04667000
- Testing
- Forced Air Warming
- Where
- Turkey (Türkiye)
- Volunteers
- 35 people, healthy volunteers welcome
- Sponsor
- Hacettepe University
Postoperative Pain
Abdominal Wall Local Anesthesia to Maximize Postoperative Pain Control After Cesarean Delivery
This study has been designed to determine if women undergoing cesarean delivery with spinal anesthesia and routine pain management who also have an additional ultrasound guided transversus abdominis plane (TAP)block using…
- Trial name
- NCT01261637
- Testing
- Ropivicaine
- Where
- Canada
- Volunteers
- 86 people, healthy volunteers welcome
- Sponsor
- IWK Health Centre
Cesarean Section, Pain, Postoperative
Deep Tissue Massage on Pain and Comfort After Cesarean
The aim of this study to determine the effect of deep tissue massage applied to the back on pain and comfort after cesarean section.
- Conditions
- Cesarean Section, Pain, Postoperative, Massage, Comfort
- Trial name
- NCT04457921
- Testing
- deep tissue massage
- Where
- Turkey (Türkiye)
- Volunteers
- 81 people, healthy volunteers welcome
- Sponsor
- Inonu University
IUD Insertion
Sub Lingual Misoprostol Before IUD Insertion in Women With Only Previous Cesarean Section
The aim of the work is to evaluate the efficacy of the sub lingual prostaglandin E1 synthetic analogue (misoprostol) before IUD insertion to facilitate the procedure in patients delivered before only by cesarean section.
- Trial name
- NCT02141321
- Testing
- Misoprostol
- Where
- Egypt
- Volunteers
- 124 people, healthy volunteers welcome
- Sponsor
- Ain Shams University
Quality of Life, Breastfeeding
Quality of Recovery in Parturients Consumed Preoperative Carbohydrate Fluid for Elective Cesarean Delivery
The establishment of the Enhanced Recovery After Cesarean protocols resulted in to the production of specific care pathways with the aim of optimizing recovery after cesarean delivery (CD) and to reduce the costs to the health…
- Conditions
- Quality of Life, Breastfeeding, Postoperative Pain, Postoperative Nausea
- Trial name
- QoR-10 (NCT05841693)
- Testing
- Carbohydrate
- Where
- Turkey (Türkiye)
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Karamanoğlu Mehmetbey University
Preoperative Anxiety, Postpartum Pain
QR Code-Based Preoperative Education for Cesarean Birth: Anxiety, Pain, and Comfort
This study aims to evaluate the effect of QR code-based preoperative education on anxiety, postpartum pain, and comfort levels in women undergoing cesarean birth.
- Conditions
- Preoperative Anxiety, Postpartum Pain, Maternal Comfort, Cesarean Birth
- Trial name
- NCT07368387
- Testing
- QR Code-Based Preoperative Education
- Volunteers
- 88 people, healthy volunteers welcome
- Sponsor
- Karabuk University
Post-operative Pain, Opioid Use
RCT of Counseling Intervention on Post-op Opiate Use
This study is a randomized controlled trial to investigate the effect of a simple counseling intervention on post-operative narcotic requirements, with the hypothesis that women receiving this intervention will use fewer…
- Conditions
- Post-operative Pain, Opioid Use, Cesarean Section
- Trial name
- NCT03359798
- Testing
- Narcotic counseling script, Post-partum depression counseling script
- Volunteers
- healthy volunteers welcome
- Sponsor
- Brigham and Women's Hospital
Blood Loss, Repeat Cesarean Section
Cesarean Scar Pregnancy and Clinical Outcomes
This study is a prospective cohort study, led by Prof. Zhao Yangyu, from the Department of Gynecology \& Obstetrics, Peking University Third Hospital.
- Conditions
- Blood Loss, Repeat Cesarean Section, Maternal Transmission, Hysterectomy
- Trial name
- NCT05481606
- Volunteers
- 500 people, healthy volunteers welcome
- Sponsor
- Peking University Third Hospital
Elective Cesarean Section, Preeclampsia
Ultrasonography for Fluid Assessment in Parturients With Preeclampsia Undergoing Cesarean Section
Preeclampsia is a multifocal syndrome reported in 2-8 % of pregnancies. It is diagnosed in the second half of pregnancy by two separate measurements of systolic blood pressure ≥140 mmHg and/or a diastolic blood pressure ≥ 90 mmHg…
- Trial name
- NCT04370847
- Testing
- Spinal Anesthesia, Intrathecal Bupivacaine, Intrathecal Fentanyl
- Where
- Egypt
- Volunteers
- 100 people
- Sponsor
- Mansoura University
Ssc, Cesarean Birth
Evaluation of the Effect of Immediate and Early Skin-to-Skin Contact After Cesarean on Maternal and Neonatal Parameters in the First 24 Hours: A Quasi-Experimental Study
This study was carried out as a quasi-experimental study to determine the effects of immediate and early skin-to-skin contact (SSC) applied between mother and newborn after cesarean on breastfeeding, anxiety, bleeding and newborn…
- Conditions
- Ssc, Cesarean Birth, Neonate, Breastfeeding
- Trial name
- SSC (NCT07531758)
- Testing
- skin to skin contact
- Where
- Turkey (Türkiye)
- Volunteers
- 92 people, healthy volunteers welcome
- Sponsor
- Çankırı Karatekin University
Quality of Recovery, Cesarean Section
Relationship Between Analgesia Techniques and Post-cesarean Recovery Quality
The question remains whether the patients in whom USG-guided regional anesthesia and analgesia techniques are applied have a better recovery score than subarachnoid morphine administration, which is considered the gold standard.
- Trial name
- NCT05181358
- Where
- Turkey (Türkiye)
- Volunteers
- 180 people, healthy volunteers welcome
- Sponsor
- Konya Meram State Hospital
Myofascial Release, Deep Friction Massage
Effect of Myofascial Release Versus Deep Friction Massage on Abdominal Recovery and Scar After Cesarean Section
This study was done to compare the effect of myofascial release versus deep friction massage on abdominal recovery and scar after cesarean section.
- Conditions
- Myofascial Release, Deep Friction Massage, Cesarean Section Complications, Scar
- Trial name
- NCT07130747
- Testing
- Myofascial release, Deep friction massage, Routine daily scar care advices
- Where
- Egypt
- Volunteers
- 36 people
- Sponsor
- Cairo University
Cesarean Delivery; Neuraxial Opioids
Respiratory Rate After Cesarean Delivery
The study proposal summarizes aspects related to respiratory rate in women who undergo spinal anesthesia for cesarean delivery who receive or do not receive neuraxial opioids
- Trial name
- NCT04250233
- Testing
- Respiratory Monitor
- Where
- Israel
- Volunteers
- 80 people
- Sponsor
- Tel-Aviv Sourasky Medical Center
Placenta Previa
17-Alpha-Hydroxyprogesterone Caproate in Pregnant Women With Placenta Previa
Purpose to evaluate the effects of intramuscular 17-Alpha-Hydroxyprogesterone Caproate (17-OHPC) for prevention of Emergent Cesarean Delivery in symptomatic Pregnant Women with Placenta Previa
- Trial name
- NCT03779438
- Testing
- 17-OHPC
- Where
- Egypt
- Volunteers
- 300 people
- Sponsor
- Aswan University Hospital