CompletedNot Applicable

Analgesic Effects of Intrathecal Morphine and Transversalis Plane Block After Cesarean Delivery

Turkey (Türkiye)117 participantsStarted 2025-11-15

Plain-language summary

A comparison of postoperative pain levels, patient satisfaction, and side effects is planned between patients who received morphine during spinal anesthesia for cesarean section and patients who did not receive morphine but underwent bilateral transverse fascial plane block.

Who can participate

Age range

18 Years – 45 Years

Sex

FEMALE

See this in plain English?

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

Inclusion Criteria: * Woman aged 18-45 * ASA physical status II * Patients undergoing cesarean section under spinal anesthesia * Patients received intrathecal morphine and bilateral TFB block. Exclusion Criteria: * Contraindications to spinal anesthesia * ASA physical statu III- IV * History of hypersensitivity or allergy to the study drugs * Pregnancy-related diseases ( preeclampsia, eclampsia, gestational diabetes, gestational hypertension, placental abnormalities vb) * Obesity (body mass index \> 35 kg/m2) * Cognitive impairment or inability to cooperate * Alcohol or drug dependence * Patients who do not provide informed consent

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Pain intensity assessed by Numeric Rating Scale (NRS)

Timeframe: 2nd, 6th, 12th, and 24th hours postoperatively

Trial details

NCT IDNCT07490795

SponsorVezirköprü State Hospital

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2025-11-15

View on ClinicalTrials.gov More Caesarean Section trials