Clinical trials: Emergency Caesarean
Pain
The Evaluation of Postoperative Pain After Caesarean Section
The aim of this study is to determine the effect of surgical priority either emergency or elective on postoperative pain in caesarean section operations.
- Trial name
- NCT02332395
- Where
- Turkey (Türkiye)
- Volunteers
- 115 people
- Sponsor
- Tokat Gaziosmanpasa University
Post-traumatic Stress Disorder (PTSD), Postpartum Mental Health
A Computer Game for Postpartum Mental Health After Emergency Cesarean Birth
This study aims to explore whether playing the computer game Tetris can reduce PTSD symptoms in women who have undergone emergency caesarean births.
- Trial name
- NCT07290127
- Testing
- implementation of a brief computer-based intervention "Tetris"
- Where
- Japan
- Volunteers
- 120 people, healthy volunteers welcome
- Sponsor
- Kyoto University, Graduate School of Medicine
Caesarean Section
Sensitivity of Hyomental Distance Ratio as a Single Predictor of Difficult Intubation in Obstetrics
This is a study to detect the sensitivity of thyromental distance ratio as a single predictor for difficult intubation in patients undergoing cesarean section under general anesthesia.
- Trial name
- HMDR (NCT00916812)
- Where
- United Arab Emirates
- Volunteers
- 188 people
- Sponsor
- King Khaled Eye Specialist Hospital
Caesarean Section
Ropivacaine 0.75% Versus Levobupivacaine 0.5% for Conversion of Labour Epidural
The aim of this trial is to compare the local anaesthetic ropivacaine to local anaesthetic levobupivacaine in converting the standard patient controlled labour epidural to provide anaesthesia for an emergency Caesarean section.
- Trial name
- RoLe (NCT01160965)
- Testing
- 0.5% levobupivacaine, 0.75% Ropivacaine
- Where
- United Kingdom
- Sponsor
- Guy's and St Thomas' NHS Foundation Trust
Surgical Wound, Surgical Wound Infection
Caesarean Wound Dressing Removal Study
An open labelled randomised trial on the timing of wound dressing removal for emergency caesarean delivery in labour.
- Conditions
- Surgical Wound, Surgical Wound Infection, Cesarean Section Complications
- Trial name
- Cesarean (NCT05458518)
- Testing
- Cesarean wound dressing removal
- Where
- Malaysia
- Volunteers
- 294 people, healthy volunteers welcome
- Sponsor
- Hospital Kemaman
Nonreassuring Fetal Status
Acute Tocolysis With Terbutaline for Suspected Fetal Distress
The trial was to determine the effect of administrating subcutaneous terbutaline prior to emergency caesarean delivery for suspected fetal distress
- Trial name
- NCT05326269
- Testing
- Terbutaline
- Where
- Malaysia
- Volunteers
- 100 people, healthy volunteers welcome
- Sponsor
- Hospital Kemaman
Postpartum Hemorrhage (Primary)
Carbetocin Versus Oxytocin for the Prevention of Postpartum Hemorrhage in Emergency Caesarean Delivery
Postpartum haemorrhage keeps to be the leading cause of maternal mortality in middle and low-income countries, including Iraq. Much advancement had been made in the field of treatment for postpartum haemorrhage but no much…
- Trial name
- NCT03755531
- Testing
- Carbetocin, Oxytocin
- Where
- Iraq
- Volunteers
- 300 people
- Sponsor
- Al-Kindy College of Medicine
Pregnancy Related
Enhanced Recovery After Surgery for Emergency Caesarean Deliveries
Caesarean section (CS) constitutes a large proportion of the total surgical volume in low-income countries. This rate comes with challenges including surgical complications, shortage of beds, and consequently long waiting time…
- Trial name
- ERAS-Mbarara (NCT03518463)
- Testing
- Enhanced recovery after surgery (ERAS)
- Where
- Uganda
- Volunteers
- 160 people
- Sponsor
- Mbarara University of Science and Technology
Cesarean Wound Disruption, Cesarean Section; Infection
Delayed Primary Closure of Skin in Emergency Caesarean Section
Pregnant mothers requiring emergency cs with history of ruptured membranes would be allocated randomly into two groups in an aim to study the comparative outcome of different methods of skin closure namely primary and delayed…
- Trial name
- NCT04587960
- Testing
- Delayed primary closure of skin incision in Caesarean section in experimental group, Primary closure of skin incision in Caesarean section in active comparator group
- Where
- India
- Volunteers
- 70 people
- Sponsor
- Dr.Jhuma Biswas
Pregnancy, Anaesthesia
Audit of the Response Time of the Anaesthetic and Surgical Techniques for Crash Caesarean Section
A decision-to-delivery interval of 30 minutes for category-1 Caesarean section deliveries is the standard of practice recommended by clinical guidelines.
- Trial name
- Crash (NCT02314078)
- Where
- Singapore
- Volunteers
- 390 people
- Sponsor
- KK Women's and Children's Hospital
Postpartum Hemorrhage \(PPH\)
Comparison of the Effect of Carbetocin Versus Oxytocin in the Prevention of Postpartum Hemorrhage After Emergency Caesarean Section in Antenatal Low-risk Patients
This study will be conducted to compare the effects of pabal and oxytocin administered to prevent postpartum hemorrhage in patients who were followed in the delivery room due to vaginal labor but underwent cesarean section due to…
- Trial name
- EMERGE-CS (NCT07380529)
- Testing
- Carbetocin, Oxytocin
- Where
- 2 sites in Turkey (Türkiye)
- Volunteers
- 300 people, healthy volunteers welcome
- Sponsor
- Ankara Etlik City Hospital
Anesthesia; Adverse Effect, Newborn Morbidity
Does the Mode of Anesthesia Affect the Feto-maternal Outcome in Category-1 Caesarean Section
Spinal anesthesia (SA) has become the standard technique in elective cesarean section (CS) as it results in less maternal and neonatal morbidity than general anesthesia (GA) (Grade-A recommendation, NICE).
- Trial name
- NCT04634981
- Testing
- anesthesia of emergency cesarean section
- Where
- Egypt
- Volunteers
- 74 people
- Sponsor
- Benha University
Emergency Caesarean
Bicarbonate Epidural Injection in Emergency Caesarian
During labor, pain is systematic. In France, epidural analgesia is the gold standard to fight pain. Sometimes, emergency situations involve the maternal or fetal prognosis and require an emergency fetal extraction by caesarean.
- Trial name
- BiEpIC (NCT04255121)
- Testing
- 2% adrenaline lidocaine associated with 4.2% sodium bicarbonate, 2% adrenaline lidocaine
- Where
- France
- Volunteers
- 400 people
- Sponsor
- CHU de Reims
Neonatal Distress
Caesarean and Corticotherapy
Comparison of two randomized group : caesarean section planned at 38 weeks after 2 antenatal injections of 12 mg of betamethasone 48 h before. caesarean section planned at 39 weeks without corticosteroid.
- Trial name
- NCT00446953
- Testing
- betamethasone
- Where
- 5 sites in France
- Volunteers
- 200 people
- Sponsor
- University Hospital, Strasbourg, France