Clinical trials: Complications; Cesarean Section
Pregnancy, Multiple
Perineal Consequences of Twin Pregnancies According to Mode of Delivery
This is an ancillary study to the "JUMODA" (National Prospective and Comparative Study on the Mode of Delivery of Twins) study: please see NCT01987063.
- Trial name
- JUMODA-CP (NCT02059746)
- Testing
- Questionnaires sent by mail
- Where
- 2 sites in France
- Volunteers
- 3,039 people
- Sponsor
- Centre Hospitalier Universitaire de Nīmes
High Risk Pregnancy, Cesarean Wound Disruption With Postnatal Complication
Negative Pressure Wound Therapy to Prevent Wound Complications Following Cesarean Section in High Risk Patients
This is a randomized controlled trial. Patients with a condition that increases their risk of a wound complication will be approached for inclusion in the trial.
- Trial name
- NCT03082664
- Testing
- PICO Single Use Negative Pressure Wound Therapy
- Where
- United States
- Volunteers
- 154 people
- Sponsor
- University of Arizona
Cesarean Section Complications, ERAS
Outcomes of Enhanced Recovery After Cesarean (ERAC) Protocol
In recent years, a set of evidence-based recommendations called Enhanced Recovery After Surgery (ERAS) is being applied for care of cesarean sections.
- Trial name
- NCT05786352
- Testing
- ERAS protocol
- Where
- Turkey (Türkiye)
- Volunteers
- 1,200 people
- Sponsor
- Zeynep Kamil Maternity and Pediatric Research and Training Hospital
Cesarean Section; Infection, Surgical Site Infection
Vaginal Preparation With Chlorhexidine-alcohol vs. Povidine-iodine vs. Saline
The purpose of this study is to see whether chlorhexidine is superior to povidine-iodine vaginal antisepsis at reducing bacteria colony counts in pregnant women by comparing three groups: vaginal washing with…
- Trial name
- NCT03640507
- Testing
- Chlorhexidine-alcohol, Povidine-iodine, Sterile saline
- Where
- United States
- Volunteers
- 30 people
- Sponsor
- Columbia University
Post Operative Pain, Caesarean Section
Naldebain® Extended-release Injection After Cesarean Section in Pain Management
Cesarean section is one of the surgeries most commonly leading to postoperative severe acute pain. It was reported that the mean worst pain intensity reached to 6.14 one day after cesarean section in Germany.
- Conditions
- Post Operative Pain, Caesarean Section, Analgesia
- Trial name
- NCT05446311
- Testing
- Dinalbuphine sebacate
- Volunteers
- 20 people
- Sponsor
- Tri-Service General Hospital (TSGH)
Midazolam, Pre-eclampsia
Midazolam Efficacy/Safety in Pre-Eclamptic C-Section Sedation
This study will compare four different doses of midazolam (0 mg/kg, 0.01 mg/kg, 0.02 mg/kg, and 0.03 mg/kg) administered intravenously to women with pre-eclampsia undergoing cesarean section.
- Conditions
- Midazolam, Pre-eclampsia, Cesarean Section, Efficacy
- Trial name
- NCT07021521
- Testing
- 0 mg/kg Midazolam (Control Group), 0.01 mg/kg Midazolam Group, 0.02 mg/kg Midazolam Group
- Where
- China
- Volunteers
- 124 people
- Sponsor
- Zhuji People's Hospital of Zhejiang Province
Post-operative Pain, Acute, Cesarean Section
Management of Postoperative Pain After Cesarean Delivery Using Bridge Auricular Percutaneous Nerve Field Stimulator
Post-cesarean section (CS) pain is commonly treated with acetaminophen, ibuprofen, and opioid medications as needed following delivery.
- Conditions
- Post-operative Pain, Acute, Cesarean Section, Opioid Use Disorder, Opioids; Harmful Use
- Trial name
- NCT06434714
- Testing
- Auricular percutaneous nerve field stimulator
- Where
- United States
- Volunteers
- healthy volunteers welcome
- Sponsor
- Inova Health Care Services
Maternal Complications After Oral Anticoagulation When Initiated Early and Late After Caesarean Section Done for Patients With Mechanical Heart Valve Prosthesis
Early Versus Late Post Caesarean Section Oral Anticoagulation Initiation and Risk of Maternal Complications in Patients With Mechanical Heart Valve Prosthesis
A randomized cohort study applied to patients with mechanical heart valve prosthesis who will be delivered by caesarean section at or after 28 weeks of gestation .
- Trial name
- NCT04855110
- Testing
- Warfarin Sodium started on Day 2 after caesarean section (in a dose that achieves a therapeutic level as indicated by the cardiology consultant), Warfarin Sodium started on day 5 after caesarean section (in a dose that achieves a therapeutic level as indicated by the cardiology consultant)
- Where
- Egypt
- Volunteers
- 114 people
- Sponsor
- Cairo University
Postanesthetic Excitement, Cesarean Section
Dexmedetomidine Compared to Ondansetron for Postanaesthetic Shivering in Patients Undergoing a Cesarean Section
Evaluate the efficiency of management with intravenous dexmedetomidine compared to intravenous ondansetron to achieve the disappearance of post-anesthetic shivering in a shorter time in the obstetric patient undergoing cesarean…
- Trial name
- NCT06289335
- Testing
- saline solution
- Where
- Mexico
- Volunteers
- 40 people
- Sponsor
- Hospital Central "Dr. Ignacio Morones Prieto"
Cesarean Section Complications
The Efficacy of Transversus Abdominis Plane Block Versus Wound Infiltration for Analgesia After Cesarean Delivery:
This study aimed to compare bilateral ultrasound-guided TAP block with single-shot local anesthetic wound infiltration for analgesia after cesarean delivery performed under spinal anesthesia
- Trial name
- TAPBLOCK (NCT04874168)
- Testing
- TAP block
- Where
- Egypt
- Volunteers
- 210 people
- Sponsor
- Ain Shams University
Post Partum Hemorrhage
Can Tranexamic Acid Reduce Bleeding After Post Partum Hemorrhage in Cesarean Section Delivery
The purpose of this study was to evaluate the effect of early administration of tranexamic acid (TXA) on post partum hemorrhage caused by uterine atony after cesarean section delivery.
- Trial name
- NCT01599468
- Testing
- Tranexamic Acid, saline serum
- Where
- Tunisia
- Volunteers
- 74 people
- Sponsor
- Hédi Chaker Hospital
Complication of Anaesthesia During Labour and Delivery
Plethysmographic Variability Index in Post Spinal Anesthesia Hypotension in Cesarean Section
Full term pregnant female patients presented for elective C.S for single viable fetus will be included in this study. Before anesthesia, the patient will be attached to a monitor of: ECG , heart rate, non invasive blood pressure…
- Trial name
- NCT04010318
- Testing
- Spinal Anesthesia
- Where
- 2 sites in Egypt
- Volunteers
- 100 people
- Sponsor
- Tanta University
Surgical Site Infection (SSI)
A Randomized Controlled Trial Comparing the Incidence of Surgical Site Infections in Cesarean Section With and Without Subcutaneous Drain Placement at Queen Savang Vadhana Memorial Hospital
To study and compare the incidence of surgical site infection after cesarean section in pregnant women with subcutaneous wound drainage and those without subcutaneous wound drainage at Queen Savang Vadhana Memorial Hospital…
- Trial name
- NCT07395518
- Testing
- Radivac drain
- Where
- Thailand
- Volunteers
- 86 people
- Sponsor
- Queen Savang Vadhana Memorial Hospital, Thailand
Intraoperative Awareness
Effect of Remifentanil on the Bispectral Index in Women Undergoing Caesarean Delivery Under General Anaesthesia
Patients undergoing caesarean delivery under inhalation anaesthesia are at a high risk of awareness, especially in the period before delivery.
- Trial name
- NCT03508102
- Testing
- remifentanil
- Volunteers
- 60 people
- Sponsor
- West China Second University Hospital
Hypotension During Cesarean Delivery, Postoperative Nausea and Vomiting (PONV)
Dexamethasone to Prevent Side Effects of Spinal Anesthesia in Cesarean Delivery
The goal of this clinical trial is to evaluate the effectiveness of intravenous dexamethasone in preventing adverse effects of spinal anesthesia and prolonging postoperative analgesia in parturients undergoing elective cesarean…
- Conditions
- Hypotension During Cesarean Delivery, Postoperative Nausea and Vomiting (PONV), Pain, Postoperative
- Trial name
- NCT07615595
- Testing
- Dexamethasone
- Where
- Vietnam
- Volunteers
- 176 people
- Sponsor
- University Medical Center Ho Chi Minh City (UMC)
Post Operative Hemorrhage
Mechanical Dilatation of the Cervix at Elective Caesarean Section to Reduce Post-Operative Blood Loss
obstetric hemorrhage remains one of the major causes of maternal death in both developed and developing countries. Because of its importance as a leading cause of maternal mortality and morbidity, and because of evidence of…
- Trial name
- NCT03444792
- Testing
- mechanical dilatation of the cervix
- Where
- Egypt
- Volunteers
- 774 people
- Sponsor
- Cairo University
Complications; Cesarean Section
Oxytocin to Decrease Blood Loss During Cesarean Section
The goal of this study is to determine the best dose of a drug called oxytocin, that is usually used to stop bleeding during a delivery, when used during a cesarean delivery.
- Trial name
- NCT00891150
- Testing
- Oxytocin
- Where
- Lebanon
- Volunteers
- 200 people, healthy volunteers welcome
- Sponsor
- American University of Beirut Medical Center
Cesarean Section Complications, Hypotension
Noninvasive Continuous Blood Pressure Monitoring for Cesarean Delivery
Noninvasive continuous blood pressure monitoring for preventing post-spinal hypotension during cesarean delivery: A randomized controlled trial
- Trial name
- NCT04752904
- Testing
- ClearSight System
- Where
- South Korea
- Volunteers
- 154 people
- Sponsor
- Seoul National University Hospital
Post Operative Pain, Cesarean Section Complications
Quercetin Effect on Post-ceserean Pain
The cesarean section is a common gynecological surgery, requiring effective pain management to prevent complications and immobility.
- Trial name
- NCT06650891
- Testing
- Quercetin
- Where
- Egypt
- Volunteers
- 80 people
- Sponsor
- Future University in Egypt
Complications of Pregnancy, Childbirth and the Puerperium
Non-Invasive Hemoglobin Monitoring of Women Undergoing Cesarean Delivery
The purpose of this study is to determine the normal hemoglobin curve during cesarean delivery and for the first 24 hours after surgery to aid in the creation of an algorithm to detect life-threatening bleeding earlier.
- Trial name
- NCT02275507
- Testing
- Masimo Rainbow Sensor
- Where
- United States
- Volunteers
- 50 people, healthy volunteers welcome
- Sponsor
- Stony Brook University
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