The Analgesic Efficacy of Perineural Nalbuphine as an Adjuvant to Bupivacaine in Ultrasound Guided Superficial Cervical Plexus Nerve Block for Thyroid Surgeries. A Double Blinded Randomized Controlled Trial.
Condition(s) studied
Investigational drug(s) / intervention(s)
Adding perineural Nalbuphine to Bupivacaine in superficial cervical nerve block: Adding nalbuphine as an adjuvant to bupivacaine in superficial cervical plexus block during thyroid surgeries
Study summary
This study aiming to evaluate the analgesic effect of adding nalbuphine as an adjuvant to bupivacaine in superficial cervical plexus block during thyroid surgeries regarding first rescue analgesia in the first twenty-four hours postoperative, VAS score after extubation and complications such as postoperative nausea, vomiting and respiratory depression.
Eligibility
Primary outcome measure(s)
- time to first rescue analgesia (will be given to VAS score > 4) following surgery in the first 24 hours. — First 24 hours postoperative
defined as the time interval between the end of surgery and the first request to postoperative Nalbuphine
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Kasr Alainy Teaching Hospitals | Giza | الجيزة | Recruiting |
More Cairo University trials in Egypt
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06633068 on ClinicalTrials.gov ↗ ← All trials in Egypt