CompletedNot Applicable

Compared With Different Method for Postcesarean Section Analgesia

Turkey (Türkiye)46 participantsStarted 2022-06-16

Plain-language summary

The aim of this study is compare the efficacy of local anesthetic infiltration into all layers of the anterior abdominal wall and peritoneal instillation and intrathecal injection of morphine with local anesthesic to reduce pain in women undergoing elective cesarean section under spinal anesthesia. The primary outcome is to compare the total amount of opioids consumed in the first 24 hours postoperatively. Secondary purpose; Pain scores at 2,4,6,12,and 24 hours during movement ( moving back and forth in bed ) and rest ( lying motionless in bed )

Who can participate

Age range18 Years – 50 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 * 18-50 age * ASA II * Fullterm singular pregnancy Exclusion Criteria: * Neuraxial anesthesia is contraindicated, * Allergy to the drugs to be used in the study, * Refused to participate in the study, * BMI\>35 kg/m2 * ASA≥3 * Diabetes * Preeclampsia, * Cardiovascular disease * Chronic pain and neuropathic pain, * Given opioids in the operation due to intraoperative pain, * Switched to general anesthesia, * Excessive bleeding during the operation, * Uterine atony * Drain placed in the area to be infiltrated, * History of drug addiction and psychiatric illness, * Understand Visual analog pain scale

What they're measuring

The primary outcome is to compare the total amount of opioids consumed in the first 24 hours postoperatively.

Timeframe: postoperative 24 hours

Trial details

NCT IDNCT05405049

SponsorAtaturk University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-10-25

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