Clinical trials: Cesarian Section
Pregnancy, Cesarean Section
A Comparison of Manual vs. Spontaneous Removal of the Placenta at Cesarean Section
The purpose of this study is to determine if there are differences in operative blood loss with manual vs. spontaneous removal of the placenta during cesarean section.
- Trial name
- NCT00375986
- Testing
- Manual placental removal at Cesarean delivery, Spontaneous placental removal at Cesarean delivery
- Where
- United States
- Volunteers
- 150 people
- Sponsor
- University of Rochester
Cesarean Section
Effects of Back Massage After Cesarean Section
The aim of this study is to examine the effect of back massage application after cesarean section on women's pain, anxiety, sleep, breastfeeding, comfort, uterine involution process and physiological parameters.
- Trial name
- NCT06162156
- Testing
- Back massage
- Where
- Turkey (Türkiye)
- Volunteers
- 78 people, healthy volunteers welcome
- Sponsor
- Ordu University
Caesarean Sections, Augmentation With Oxytocin
The Labour Progression Study, a Cluster Randomised Trial on Labour Progression for First Time Mothers
The purpose of this study is to evaluate if the rate of emergency caesarean section can be reduced if adhering to a dynamic labour progression curve compared to a static progression curve for first time mothers without…
- Conditions
- Caesarean Sections, Augmentation With Oxytocin, Labour Dystocia
- Trial name
- LAPS (NCT02221427)
- Testing
- Dynamic progression curve, Static labour progression curve (F)
- Where
- Norway
- Volunteers
- 6,582 people, healthy volunteers welcome
- Sponsor
- Ostfold Hospital Trust
Communication
Placebo Versus Nocebo: Effects on Pain and Anxiety During Local Anaesthetic Infiltration in Parturient Undergoing Elective Caesarean Delivery
This randomized trial compared placebo and nocebo effect over anaesthetist-patient communication on pain and anxiety score during local anaesthetic (LA) skin infiltration in parturient undergoing caesarean delivery under regional…
- Trial name
- NCT04975659
- Where
- Malaysia
- Volunteers
- 76 people
- Sponsor
- Universiti Kebangsaan Malaysia Medical Centre
Cesarean Section
The Effect of Pre-Cesarean Section Guided Imagery
The aim of this study is to evaluate the effect of guided imagery applied before cesarean section on preoperative anxiety, fear and physiological parameters. The study will be carried out in two different groups.
- Trial name
- NCT05790954
- Testing
- Guided imagery
- Where
- Turkey (Türkiye)
- Volunteers
- 60 people, healthy volunteers welcome
- Sponsor
- Menekşe Nazlı AKER
Cesarean Birth
The Cesarean Study: Optimizing Cesarean Sections and Improving Patient-Healthcare Provider Trust Using Evidence Informed Recommendations
Cesarean section (CS) rates have rapidly increased worldwide, with projections suggesting that by 2030, one in every three births will be by CS (1).
- Trial name
- CS (NCT07759622)
- Testing
- Cesarean Bundle
- Where
- Sweden
- Volunteers
- 260 people, healthy volunteers welcome
- Sponsor
- Lund University
Hypothermia, Newborn
Influence of Duration Since Birth Until Admission to Well-baby Nursery on Neonatal Temperature at Admission
The investigators will collect the time interval from birth to arrival to WBN or NICU, the time interval from arrival to nurse admission, the first measured temperature, and the week of birth.
- Trial name
- NCT05505903
- Testing
- Temerature measurement
- Where
- Israel
- Volunteers
- 2,412 people, healthy volunteers welcome
- Sponsor
- Hillel Yaffe Medical Center
Haemorrhage
Comparing Blood Loss During Caesarean Section Between Manual Separation of Placenta & Conservative Management
to compare the blood loss during caesarean section between two different methods of separating the placenta after fetal extraction, keeping in mind that most blood loss occurs after placental separation.
- Trial name
- NCT02480556
- Testing
- manual seperation of the placenta, Conservative separation of placenta
- Where
- Egypt
- Volunteers
- 838 people, healthy volunteers welcome
- Sponsor
- Kasr El Aini Hospital
Postpartum Hemorrhage
Oxytocin Administration During Cesarean Section
Cesarean delivery is defined as fetal birth through incisions in the abdominal wall and the uterine wall. This definition does not include removal of the fetus from the abdominal cavity in the case of uterine rupture or in the…
- Trial name
- NCT03344302
- Testing
- Oxytocin
- Where
- Egypt
- Volunteers
- 200 people
- Sponsor
- Assiut University
Pregnancy Complications, Hemorrhage
Tranexamic Acid to Reduce Blood Loss in Hemorrhagic Caesarean Delivery
TRACES trial is a multicenter randomized double blind placebo control therapeutic and pharmaco-biological dose ranging study to measure the effect on blood loss reduction of a single intravenous infusion of two doses regimens…
- Trial name
- TRACES (NCT02797119)
- Testing
- tranexamic acid 1 g (TA1), tranexamic acid 0.5 g (TA1/2), Saline Solution (TA0)
- Where
- 5 sites in France
- Volunteers
- 225 people, healthy volunteers welcome
- Sponsor
- University Hospital, Lille
Cesarean Section Complications
Tranexamic Acid for the Control of Blood Loss at Elective Cesarean Section
The aim of the study is to determine, out of two doses (a standard and a low dose) compared to placebo, the optimal and minimal dose of an intravenously administered single bolus of tranexamic acid(TA) to reduce blood loss when…
- Trial name
- NCT03710330
- Testing
- normal saline, 1gm tranexamic acid, 0.5 gm tranexamic acid
- Where
- Egypt
- Volunteers
- 360 people
- Sponsor
- Aswan University Hospital
Morbid Obesity
The Ultrasound Guided Versus Land-mark Location Method for Performing Spinal Anesthesia in Obese Parturients
This study will be investigated whether an ultrasound-assisted technique is better than a classical land-mark technique to facilitate spinal anesthesia in the lateral position in morbidly obese pregnant women with BMI ≥ 40 who…
- Trial name
- NCT05342922
- Testing
- Ultrasound group, Landmark group
- Where
- Turkey (Türkiye)
- Volunteers
- 80 people, healthy volunteers welcome
- Sponsor
- Karaman Training and Research Hospital
Postoperative Pain
Intrathecal Morphine for Cesarean Delivery
This is a randomized double blinded non-inferiority study comparing the duration of pain relief when patients receive one of three doses of spinal morphine.
- Trial name
- NCT05069012
- Testing
- Morphine Sulfate
- Where
- United States
- Volunteers
- 72 people
- Sponsor
- Beth Israel Deaconess Medical Center
Pain, Postoperative
Effect of Adding Hyaluronidase to Bupivacaine in Transversus Abdominis Plane Block for Cesarean Section
Since TAP block needs to affect several nerves in single tissue plane with a single prick, hyaluronidase is expected to aid greatly in the spread of the LA and help the block.
- Trial name
- NCT05671172
- Testing
- Hyaluronidase, Bupivacaine Injection
- Where
- Egypt
- Volunteers
- 114 people
- Sponsor
- Benha University
Anesthesia
Impact of Sub-anesthetic Dose of Ketamine on Post Spinal Hypotension in Caesarean Delivery
The purpose of this study is to evaluate the effect of sub anesthetic dose of ketamine on vasopressor (Ephedrine) requirement to prevent maternal hypotension after spinal anesthesia in caesarean section.
- Trial name
- NCT03624166
- Testing
- Ketamine, isotonic saline
- Where
- Egypt
- Volunteers
- 80 people
- Sponsor
- Ain Shams University
Postpartum Complication
Multiparas Attitude to Outpatient Cesarean Section
The main purpose of this study is to explore multiparas attitude to outpatient care after a planned cesarean section.
- Trial name
- NCT05024370
- Where
- Denmark
- Volunteers
- 10 people, healthy volunteers welcome
- Sponsor
- Herning Hospital
Infection, Cesarean Delivery
Serum and Tissue Cefazolin Concentrations in Normal Weight Patients Undergoing Cesarean Delivery.
Patients undergoing Cesarean delivery (C-Section) with a body mass index of 30 or less will be given either 2 grams or 4 grams of an antibiotic before surgery. The antibiotic is intended to prevent infection from the surgery.
- Conditions
- Infection, Cesarean Delivery, Antibiotic Prophylaxis
- Trial name
- NCT01880112
- Testing
- Cefazolin
- Where
- United States
- Sponsor
- West Virginia University
Infection Control / Methods, Surgical Site Infection (SSI)
Preoperative Clindamycin Vaginal Cream Versus Vaginal Cleansing With Povidone-iodine on Postoperative Infections After Cesarean Section
To evaluate the effects of preoperative prophylactic administration of clindamycin vaginal cream compared to preoperative vaginal cleansing using a 10% povidone-iodine solution on postpartum infectious morbidity.
- Trial name
- SSI (NCT07474194)
- Testing
- Clindamycin vaginal cream, Vaginal preparation with povidone- iodide solution 10 %
- Where
- Egypt
- Volunteers
- 150 people
- Sponsor
- Beni-Suef University
Surgical Site Infection Following Cesarean Delivery
Comparison of Surgical Skin Preps During Cesarean Deliveries
In women that undergo non-emergency cesarean delivery, we are comparing the skin preparation solutions for best outcome of surgical site infection.
- Trial name
- NCT01870583
- Testing
- Iodine povidone, Chlorhexidine, Combination iodine and chlorhexidine
- Where
- 2 sites in United States
- Volunteers
- 1,404 people
- Sponsor
- Montefiore Medical Center
EPO Teqnique in Fetal Head Extraction
External Pop Out cs vs Conventional Method for Fetal Head Extraction in Repeatedcaesarean Section.
To establish feasibility and safety of the use of external pop out as a novel technique for foetal head delivery during c s, the effect of application of this method on a previously scarred uterus will be studied as a better way…
- Trial name
- EPO (NCT04968340)
- Testing
- conventional cs, external pop out teqnique
- Where
- Egypt
- Volunteers
- 600 people, healthy volunteers welcome
- Sponsor
- Assiut University
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