RecruitingPhase 2NCT06633068
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.
Sponsor
Cairo University
Enrollment
54 participants
Start Date
Jul 15, 2024
Study Type
INTERVENTIONAL
Conditions
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
Min Age: 18 YearsMax Age: 60 Years
Inclusion Criteria2
- Patients aged between 18 to 60 years old of both sexes undergoing elective thyroid surgery.
- ASA I and II.
Exclusion Criteria8
- 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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Interventions
DRUGAdding perineural Nalbuphine to Bupivacaine in superficial cervical nerve block
Adding nalbuphine as an adjuvant to bupivacaine in superficial cervical plexus block during thyroid surgeries
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06633068