Cesarean Clinical Trials

104 recruitingLast updated: July 25, 2026

There are 104 actively recruiting cesarean clinical trials across 27 countries. Studies span Not Applicable, Phase 4, Phase 2, Phase 3, Early Phase 1, Phase 1. Top locations include Philadelphia, Pennsylvania, United States, Cairo, Egypt, Chicago, Illinois, United States. Updated daily from ClinicalTrials.gov.


Cesarean Trials at a Glance

104 actively recruiting trials for cesarean are listed on ClinicalTrialsFinder across 6 cities in 27 countries. The largest study group is Not Applicable with 65 trials, with the heaviest enrollment activity in Philadelphia, Cairo, and Chicago. Lead sponsors running cesarean studies include Bursa City Hospital, Cairo University, and Benha University.

Browse cesarean trials by phase

Treatments under study

About Cesarean Clinical Trials

Looking for clinical trials for Cesarean? There are currently 1 studies actively recruiting participants. Clinical trials offer access to new treatments before they are widely available, and every approved therapy in use today was first tested through a clinical trial.

Below you can browse trials, sign up for alerts when new Cesarean trials open, and view eligibility criteria for each study. Each listing includes the study phase, locations, and enrollment details.

Frequently Asked Questions

Common questions about Cesarean clinical trials

A clinical trial is a carefully designed research study that tests new medical treatments, drugs, devices, or approaches in human volunteers. Every approved medication and treatment available today was proven safe and effective through clinical trials.

All clinical trials are reviewed and approved by Institutional Review Boards (IRBs) — independent committees that evaluate patient safety. Trials follow strict protocols, and your health is monitored closely throughout. You can withdraw at any time.

Not necessarily. Many trials compare the new treatment against the current standard of care, meaning all participants receive active treatment. When placebos are used, they are typically combined with standard treatment, not given alone. The trial description will always specify the design.

Under the Affordable Care Act, most private insurers are required to cover routine patient care costs during a clinical trial. The sponsor typically covers the investigational treatment itself. Medicare also covers routine costs for qualifying trials.

Yes. Participation is completely voluntary. You can withdraw at any time, for any reason, without it affecting your access to standard medical care.

Each trial has specific eligibility criteria — including age, diagnosis, disease stage, prior treatments, and general health. Browse the trials listed above and check their eligibility sections. You can also contact the trial site directly to discuss your situation.

Showing 120 of 104 trials

Recruiting

Development of a Patient-Centered Assessment Tool for Pain During Cesarean Delivery

Elective Cesarean Delivery
University Hospital, Basel, Switzerland12 enrolled1 locationNCT07409012
Recruiting
Not Applicable

Health Outcomes in C-Section Infants With Fecal Microbiota Transplantation

Fecal Microbiota TransplantationOverweight and ObesityCesarean Section
Oulu University Hospital460 enrolled1 locationNCT06282952
Recruiting
Not Applicable

Administration Of Calcium Gluconate for The Reduction of Blood Loss During Elective Cesarean Delivery

Elective Cesarean Delivery
Rambam Health Care Campus1,180 enrolled4 locationsNCT06235749
Recruiting
Phase 2

Oxytocin Pharmacokinetics and Pharmacodynamics

blood lossPost Partum HemorrhageCesarean Section Complications
University of Chicago100 enrolled2 locationsNCT05488457
Recruiting
Early Phase 1

Topical Tranexamic Acid to Reduce Blood Loss During Cesarean Delivery

cesarean deliveryHemostasisPostpartum Hemorrhage (PPH)+1 more
Wolfson Medical Center112 enrolled4 locationsNCT07362992
Recruiting
Not Applicable

Steri-Strip Application Versus Standard Wound Closure for Cesarean Section Incisions

SeromaSurgical Site InfectionCesarean Section+1 more
Riverside University Health System Medical Center610 enrolled1 locationNCT07686913
Recruiting
Not Applicable

Ondansetron Lozenge Versus Intravenous for Prevention of Shivering in Cesarean Section

PreventionShiveringCesarean Section+3 more
Tanta University90 enrolled1 locationNCT07511491
Recruiting

The Treatment Outcomes of Cesarean Scar Pregnancy

Cesarean Scar Pregnancy
Women's Hospital School Of Medicine Zhejiang University82 enrolled1 locationNCT07608094
Recruiting
Not Applicable

Analgesic Efficacy of Surgeon-administered Transversus Abdominis Plane Blocks for Caesarean Section.

Pain, PostoperativeCesarean Section Complications
University of Calgary80 enrolled1 locationNCT06324942
Recruiting
Not Applicable

Early General Anesthesia to Limit Experiences of Trauma During Cesarean Section-Pilot Study

Cesarean SectionDelivery; Trauma
University of Pennsylvania600 enrolled1 locationNCT07334418
Recruiting
Not Applicable

Wound Irrigation With Saline Versus Hypodilute-chlorhexidine After Cesarean Section (WISHES Study)

Cesarean Section ComplicationsCesarean Section; Infection
Loma Linda University400 enrolled1 locationNCT06339203
Recruiting

The Society for Obstetric Anesthesia and Perinatology Research Network General Anesthesia Registry

cesarean deliveryGeneral Anesthesia
Yale University5,000 enrolled35 locationsNCT06030063
Recruiting
Not Applicable

Obstetric Risk Assessment & Cesarean-delivery in Labor Estimation Using Artificial Intelligence

Cesarean section ratePregnancyLabor, Obstetric
Hadassah Medical Organization400 enrolled1 locationNCT07430358
Recruiting
Not Applicable

A RCT of Labor Induction at 39 Weeks in Low - Risk Women in China

cesarean delivery
Women's Hospital School Of Medicine Zhejiang University1,074 enrolled1 locationNCT07082530
Recruiting
Not Applicable

Determining the Optimal Dose of Intrathecal Morphine for Post-Cesarean Analgesia

Postoperative PainPostoperative Pain, AcuteCesarean Section+2 more
University of Ioannina100 enrolled1 locationNCT07023497
Recruiting
Not Applicable

The Effect of the Cesarean ERAS Protocol on Mother-Infant and Father-Infant Bonding: a Multicenter, Randomized Controlled Clinical Trial.

ERASMother-Infant InteractionCesarean Section+3 more
Okan University1 enrolled1 locationNCT07276126
Recruiting
Not Applicable

Comparison of the Therapeutic Effects of Vaginal Repair With Leuprorelin and Vaginal Repair in the Treatment of Cesarean Section Scar Defect

Cesarean Section; Dehiscence
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine94 enrolled1 locationNCT05206682
Recruiting

Effect of Gestational Weight Gain on Spinal Anesthesia in Elective Cesarean Delivery

cesarean deliveryRegional AnesthesiaGestational Weight Gain
Elazıg Fethi Sekin Sehir Hastanesi200 enrolled1 locationNCT07326644
Recruiting
Not Applicable

U-CaVIT Versus Standard of Care for Prevention of Atonic Postpartum Hemorrhage After Cesarean Section in High-risk Women.

cesarean deliveryPregnancy ComplicationsPostpartum Complication+4 more
Christian Haslinger70 enrolled1 locationNCT07019623
Recruiting

Intra-abdominal Pressure, Abdominal Circumference, and Spinal Block Level in Cesarean Section

PregnancyCesarean SectionElective Cesarean Section
Kutahya Health Sciences University107 enrolled1 locationNCT07406373