Actively Recruiting
Superficial Cervical Plexus Block With Either Clavipectoral Fascial Plane Block or Interscalene Brachial Block for Clavicle Surgeries Anesthesia
Led by Tanta University · Updated on 2025-03-11
60
Participants Needed
1
Research Sites
70 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study aims to evaluate and compare the efficacy and safety of ultrasound guided superficial cervical plexus block (SCPB) with either clavipectoral fascial plane block (CPB) or interscalene brachial plexus block (ISBP) as an anesthetic technique for clavicle surgeries.
CONDITIONS
Official Title
Superficial Cervical Plexus Block With Either Clavipectoral Fascial Plane Block or Interscalene Brachial Block for Clavicle Surgeries Anesthesia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 18 to 65 years.
- Both sexes.
- American Society of Anesthesiologists (ASA) physical status I or II.
- Patients with unilateral clavicular fractures undergoing elective internal fixation surgery.
You will not qualify if you...
- Coagulopathy (bleeding disorder).
- Infection at the nerve block site.
- Allergy to local anesthetics.
- Morbid obesity with body mass index over 35 kg/m2.
- Pre-existing neurological disease.
- Difficulty communicating.
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Tanta University
Tanta, El-Gharbia, Egypt, 31527
Actively Recruiting
Research Team
A
Ahmed M Aboeldahab, Master
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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