CompletedNot Applicable

Effects of Carbetocin and Oxytocin Used in Cesarean Sections on Postoperative Pain

Turkey (Türkiye)120 participantsStarted 2024-10-04

Plain-language summary

The aim of this observational study is to compare postoperative analgesic consumption in patients who received peroperative carbetocin or oxytocin. The main question it aims to answer is: . Does peroperative carbetocin use reduce postoperative analgesic consumption compared to oxytocin? Patients who receive routine uterotonic agents in caesarean section surgeries will be divided into two groups and their postoperative 24-hour analgesic consumption will be compared.

Who can participate

Age range18 Years – 45 Years

SexFEMALE

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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 with spinal anesthesia technique Exclusion Criteria: * Patients who cannot use the patient controlled analgesia (PCA) device postoperatively, * have limited intellectual function * have contraindications for spinal anesthesia

What they're measuring

Postoperative 24-hour analgesic consumption (Total tramadol mg / 24 hours )

Timeframe: 04/10/2024-04/01/2025

Trial details

NCT IDNCT06692621

SponsorAnkara City Hospital Bilkent

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2025-01-07

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