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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.

RecruitingPhase 2Ages 18 Years - 60 YearsAllCairo University
NCT06633068 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

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.

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📋 Eligibility rules (as published)
Inclusion Criteria: * Patients aged between 18 to 60 years old of both sexes undergoing elective thyroid surgery. * ASA I and II. Exclusion Criteria: * Patient refusal. * Hypersensitivity or contraindication to nalbuphine or bupivacaine. * Pregnancy or lactating mothers. * Hepatic, cardiac or renal diseases. * Bleeding disorders. * Severe neurological or psychological disorders. * Goitres with retrosternal extension. * Any anatomical disruption in the neck (ex: metastatic lymph nodes).
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What it tests

  • Adding perineural Nalbuphine to Bupivacaine in superficial cervical nerve block
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Where

1 site
Kasr Alainy Teaching Hospitals
Giza, Egypt
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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