Clinical trials: Cesarean Delivery Procedures
Cesarean Section
Sensory Block Onset: Epidural vs Dural Puncture Epidural in Cesarean Section
The goal of this clinical trial is to compare the onset of sensory block between epidural anesthesia and dural puncture epidural (DPE) in patients undergoing elective cesarean delivery.
- Trial name
- NCT07349082
- Testing
- Dural Puncture Epidural (DPE) Anesthesia, epidural anesthesia
- Where
- 2 sites in Indonesia
- Volunteers
- 72 people
- Sponsor
- Gadjah Mada University
Decrease Maternal Morbidity
Prediction of Pelvic Adhesions at Repeat Cesarean Delivery
Several methods have been used to predict adhesions after abdominal operations. High-resolution ultrasonography, magnetic resonance imaging and scar healing properties were the methods that were evaluated in the English…
- Trial name
- NCT02943148
- Testing
- Davey score for striae gravidarum
- Where
- Egypt
- Volunteers
- 300 people
- Sponsor
- Assiut University
Pregnancy Related, Delivery Complication
Hand Forceps vs. Conventional One-hand Technique for Fetal Head Extraction During Cesarean Section
The aim of the study is to assess the efficacy and safety of an innovative two-hand (hand forceps) fetal head extraction technique during the transverse cesarean sections (LTCS) by comparing with the conventional one-hand…
- Conditions
- Pregnancy Related, Delivery Complication, Cesarean Delivery Affecting Fetus
- Trial name
- Hand forceps (NCT04159857)
- Testing
- Fetal head extraction technique during the cesarean section
- Where
- United States
- Volunteers
- 52 people
- Sponsor
- The Reading Hospital and Medical Center
Cesarean Delivery
The Effectiveness of a Care Bundle to Prevent Postpartum Hemorrhage After Cesarean Delivery
Delays in the detection or inconsistent use of effective interventions of postpartum hemorrhage can result in complications or death.
- Trial name
- RE-TEAM (NCT06684080)
- Testing
- A care bundle
- Volunteers
- 52,000 people
- Sponsor
- Dunjin Chen
Cesarean Section Complications, Postpartum Hemorrhage
Obstetric Comorbidity Index in Postpartum Hemorrhage
The objective of this study is to examine the predictive capability of the Obstetric comorbidity index in the identification of severe maternal morbidity associated with postpartum hemorrhage in patients undergoing cesarean…
- Conditions
- Cesarean Section Complications, Postpartum Hemorrhage, Morbidity;Perinatal
- Trial name
- NCT06431204
- Testing
- Obstetric comorbidity index
- Where
- Thailand
- Volunteers
- 583 people
- Sponsor
- Mahidol University
Pain Management, Opioid Use
Understanding the Postpartum Pain Experience in Women of Minority Race/Ethnicity
This study will evaluate women's experiences with pain management and perceived attitudes regarding opioid use for postpartum pain management and examine differences by race/ ethnicity.
- Conditions
- Pain Management, Opioid Use, Postpartum Health, Cesarean Delivery
- Trial name
- NCT04601246
- Where
- United States
- Volunteers
- 49 people
- Sponsor
- Northwestern University
Infant, Newborn, Gut -Microbiota
Infant Microbiota Restoration With Maternal Microbes
The goal of this clinical trial is to test the ability of different bacterial products in restoring natural gut microbiota in C-section born infants.
- Conditions
- Infant, Newborn, Gut -Microbiota, Gut Dysbiosis, Cesarean Delivery Affecting Newborn
- Trial name
- MaMi (NCT07212361)
- Testing
- Probiotic
- Where
- 2 sites in Finland
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- University of Helsinki
Cesarean Section Rates
Reducing Cesarean Section Rates and Enhancing Vaginal Delivery in Greece: a Stepped-Wedge Randomized Controlled Trial
It is becoming increasingly apparent that there is an urgent need to systematically investigate the rising cesarean section (CS) rates in Greece and develop interventions to substantially reduce these rates.
- Trial name
- ENGAGE (NCT04504500)
- Testing
- HSOG guidelines application, Interactive workshops and courses, Feedback through follow-up meetings
- Where
- Greece
- Volunteers
- 6,029 people, healthy volunteers welcome
- Sponsor
- Hellenic Society of Obstetrics and Gynecology
Cesarean Delivery Affecting Fetus, Preterm Labor
Baby Smell Visual Stimulus Program Cortical and Breast Oxygenation Milk Amount Mother-Infant Attachment
In this study, the effect of infant odor and visual stimulus program applied to mothers who had delivered by cesarean section and whose babies were taken to the NICU on cortical and breast oxygenation (rSO2), amount of breast…
- Trial name
- NCT06058208
- Testing
- Olfactory stimulation, Visual stimulation
- Where
- Turkey (Türkiye)
- Volunteers
- 54 people, healthy volunteers welcome
- Sponsor
- Selcuk University
Cesarean Delivery Procedures
Randomized Controlled Trial of Bladder Flap vs.None
Objective: To compare outcomes in cesarean section patients undergoing bladder flap versus none. Hypotheses: Operative time will be reduced with the elimination of a bladder flap during cesarean delivery and intra-operative and…
- Trial name
- NCT00470288
- Testing
- bladder flap during cesarean section
- Where
- United States
- Volunteers
- 123 people, healthy volunteers welcome
- Sponsor
- Mountain Area Health Organization Center
Postpartum Hemorrhage
The Impact of "Natural" Cesarean Delivery on Peripartum Maternal Blood Loss.
Throughout the history, the neonate was dependent on maternal touch and care for survival. In modern obstetrics, with hospital care the neonates are seldom separated from their mothers after delivery.
- Trial name
- NCT02768142
- Testing
- Natural cesarean delivery, Standard cesarean delivery
- Where
- Israel
- Volunteers
- 214 people
- Sponsor
- Raed Salim
Neurodevelopmental Disorders
5-Year Follow-up of Children and Mother After Expectant Management Versus Induction of Labor in Low-risk Nulliparous Women at 39 Weeks of Gestation
In France, the rate of labor induction has markedly increased in recent years, partly following the ARRIVE trial suggesting short-term benefits of elective induction at 39 weeks in low-risk nulliparous women.
- Trial name
- FAMILY-FA (NCT07330336)
- Testing
- Questionnaires
- Where
- France
- Volunteers
- 4,200 people
- Sponsor
- University Hospital, Bordeaux
Wound
Staples Versus Suture for Cesarean Wound Closure
The objective of this randomized controlled trial is to compare wound morbidity (including disruption and infection) in surgical staples versus absorbable subcuticular suture for wound closure in cesarean deliveries.
- Trial name
- SVS (NCT01008449)
- Testing
- Surgical staples, Absorbable Surgical Suture
- Where
- United States
- Volunteers
- 398 people
- Sponsor
- University of Alabama at Birmingham
Postpartum Hemorrhage
Comparison of IV Ergonovine With IM Carboprost, With Oxytocin IV, During Cesarean Section for Failure to Progress
Patients having Cesarean section after they have been in labor for many hours bleed much more, in average twice as much, as compared with patients having an elective Cesarean section.
- Trial name
- NCT01869556
- Testing
- Oxytocin, Ergot, Carboprost
- Where
- Canada
- Volunteers
- 105 people, healthy volunteers welcome
- Sponsor
- Samuel Lunenfeld Research Institute, Mount Sinai Hospital
Cesarean Delivery, Postpartum Comfort
Post-cesarean Analgesia: Comparing Effectiveness of Staggered v. Simultaneous Therapies
Cesarean delivery is a commonly performed surgical procedure associated with worse postpartum pain when compared to vaginal birth. Uncontrolled postpartum pain is associated with increased neonatal and maternal risks.
- Conditions
- Cesarean Delivery, Postpartum Comfort, Postpartum Pain, Post-operative Pain
- Trial name
- PACESS (NCT07102641)
- Testing
- Acetaminophen, NSAID (Ketorolac/Ibuprofen)
- Where
- United States
- Volunteers
- 825 people
- Sponsor
- Thomas Jefferson University
Cesarean Section
A Study Comparing Two Different Techniques for Closing the Skin After a Cesarean Delivery
We hypothesize that the use of absorbable staples to close cesarean skin incisions will cause less pain, have better long-term cosmetic results, and result in improved patient satisfaction over standard metal staples.
- Trial name
- NCT00293683
- Testing
- Insorb absorbable skin staple
- Where
- United States
- Volunteers
- 120 people
- Sponsor
- Thomas Jefferson University
Cesarean Delivery Affecting Newborn, Obesity, Childhood
Vaginal Microbiome Seeding and Health Outcomes in Cesarean-delivered Neonates.
Neonates delivered by scheduled Cesarean Section will be randomized to receive vaginal seeding (exposing the infant to Mother's vaginal flora) or sham.
- Conditions
- Cesarean Delivery Affecting Newborn, Obesity, Childhood, Intestinal Microbiome, Microbiota
- Trial name
- NCT03298334
- Testing
- Vaginal Seeding, No Vaginal Seeding
- Where
- United States
- Volunteers
- 600 people, healthy volunteers welcome
- Sponsor
- National Institute of Allergy and Infectious Diseases (NIAID)
Pregnant Woman With Twins After 22 Weeks 0 Days of Gestation
National Prospective and Comparative Study on the Mode of Delivery of Twins
The purpose of this study is to determine the best obstetrical practices for twin delivery.
- Trial name
- JUMODA (NCT01987063)
- Where
- France
- Volunteers
- 8,979 people
- Sponsor
- Assistance Publique - Hôpitaux de Paris
Surgical Site Infection Following Cesarean Delivery, Cesarean Section Complications
Evaluation of an mHealth-CHW Tool for Post-c-section Follow-up in Rural Rwanda
Cesarean sections (c-sections) are one of the most common surgical procedures done globally. However, there has been an increase in the number of c-section related complications.
- Trial name
- NCT07369700
- Testing
- mHealth Community Health Worker Intervention for post-cesarean follow up
- Where
- Rwanda
- Volunteers
- 1,350 people
- Sponsor
- University of North Carolina, Chapel Hill
Pregnancy
Active Management Of Risk In Pregnancy At Term to Reduce Rate of Cesarean Deliveries
This is a prospective randomized cohort study of obstetric patients from Paley clinic at AEMC and from other affiliated obstetric clinics.
- Trial name
- NCT00598260
- Testing
- induction of labor
- Where
- United States
- Volunteers
- 222 people, healthy volunteers welcome
- Sponsor
- Albert Einstein Healthcare Network