NCT06319859

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

Intrathecal Non-preservative-free Morphine With Bupivacaine Versus Intrathecal Bupivacaine Alone for Analgesia in Unilateral Inguinal Hernia Repair Surgeries: A Randomized Controlled Clinical Trial.
Cairo University·Phase 3·ClinicalTrials.gov·drugNot yet recruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Pain, Postoperative
Drug/Device/Intervention
Morphine
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
Cairo University
Location
Cairo, Egypt
Timeline & enrollment
Phase
Phase 3
Start date
Mar 01, 2024
End date
Oct 01, 2024
Enrollment
50 participants
Primary outcome

Time to first analgesic requirement

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.

ICD-10 classifications
During surgical operationDuring surgical operationDuring surgical operationPain, unspecifiedPostoperative intestinal obstruction
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06319859
Type
Non-Device Trial
About this record

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.