CompletedPhase 3

Intrathecal Non-preservative-free Morphine With Bupivacaine Versus Intrathecal Bupivacaine Alone for Analgesia in Unilateral Inguinal Hernia Repair Surgeries

Egypt50 participantsStarted 2024-08-03

Plain-language summary

This study will evaluate the efficacy and safety of intrathecal non-preservative-free morphine and its effect on pain in patients undergoing unilateral inguinal hernia surgeries.

Who can participate

Age range18 Years – 65 Years

SexALL

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: * Patients aged 18-65 years old. * Both genders. * ASA I and II class. Exclusion Criteria: * Patient refusal. * Known local anesthetic (LA) allergy. * Skin lesions or infections at the site of needle insertion. * Contraindications to spinal anesthesia. * Failure of spinal anesthesia. * ASA III and VI class. * Central or peripheral neuropathies. * Severe respiratory or cardiac diseases.

What they're measuring

Time to first analgesic requirement

Timeframe: 48 hours post-operatively

Trial details

NCT IDNCT06319859

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-10-15

View on ClinicalTrials.gov More Pain, Postoperative trials