Intrathecal Non-preservative-free Morphine With Bupivacaine Versus Intrathecal Bupivacaine Alone for Analgesia in Unilateral Inguinal Hernia Repair Surgeries
- Disease/Condition
- Pain, Postoperative
- Drug/Device/Intervention
- Morphine
- Study type
- Interventional
- Intervention type
- drug
- Primary sponsor
- Cairo University
- Location
- Cairo, Egypt
- Phase
- Phase 3
- Start date
- Mar 01, 2024
- End date
- Oct 01, 2024
- Enrollment
- 50 participants
Time to first analgesic requirement
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.
- Registry
- ClinicalTrials.gov
- Trial ID
- NCT06319859
- Type
- Non-Device Trial
Access comprehensive clinical trial information for NCT06319859 through Pure Global AI's free database. This Phase 3 trial is sponsored by Cairo University and is currently Not yet recruiting. The study focuses on Pain, Postoperative. Target enrollment is 50 participants.
This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.