Last updated: March 20, 2025
Sponsor: Ankara City Hospital Bilkent
Overall Status: Completed
Phase
N/A
Condition
N/ATreatment
Oxytocin
Carbetocin
Clinical Study ID
NCT06692621
E2-234595
Ages 18-45 Female Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Pregnant women in the American Society of Anesthesiologists (ASA) II class,
who have had a previous uncomplicated cesarean delivery,
who are 18-45 years old and are planned to undergo elective cesarean section withspinal anesthesia technique
Exclusion
Exclusion Criteria:
Patients who cannot use the patient controlled analgesia (PCA) devicepostoperatively,
have limited intellectual function
have contraindications for spinal anesthesia
Study Design
Total Participants: 120
Treatment Group(s): 2
Primary Treatment: Oxytocin
Phase:
Study Start date:
October 04, 2024
Estimated Completion Date:
January 10, 2025
Study Description
Connect with a study center
Ankara Bilkent City Hospital
Ankara,
TurkeySite Not Available
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