Actively Recruiting
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.
Led by Cairo University · Updated on 2024-10-09
54
Participants Needed
1
Research Sites
50 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
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.
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients aged between 18 to 60 years old of both sexes undergoing elective thyroid surgery.
- ASA I and II physical status.
You will not qualify if you...
- Patient refusal.
- Allergy or contraindication to nalbuphine or bupivacaine.
- Pregnancy or breastfeeding.
- Liver, heart, or kidney diseases.
- Bleeding disorders.
- Severe neurological or psychological disorders.
- Goiters with retrosternal extension.
- Any anatomical abnormalities in the neck such as metastatic lymph nodes.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Kasr Alainy Teaching Hospitals
Giza, الجيزة, Egypt, 1111
Actively Recruiting
Research Team
S
Sara M Badie, Master degree
CONTACT
N
Nashwa Nabil, Professor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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