Actively Recruiting
Ultrasound Guided Superficial Cervical Plexus Block With Either Clavipectoral Fascial Plane Block or Interscalene Brachial Block for Clavicle Surgeries Anesthesia: A Randomized Controlled Trial
Led by Tanta University · Updated on 2025-03-11
60
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating and comparing two anesthesia techniques for clavicle surgeries: ultrasound guided superficial cervical plexus block (SCPB) combined with either clavipectoral fascial plane block (CPB) or interscalene brachial plexus block (ISBP). The study aims to assess the effectiveness and safety of these methods in managing pain during clavicle fracture surgeries, which are common shoulder injuries requiring precise pain control. The study involves two treatment groups. One group will receive SCPB combined with CPB, a newer regional nerve block providing analgesia to the clavicular region and upper shoulder. The other group will receive SCPB combined with ISBP, which delivers anesthesia at the brachial plexus to cover the shoulder, upper arm, and clavicular area. Both interventions use ultrasound guidance to ensure accurate delivery of anesthetic. Participants will undergo elective internal fixation surgery for unilateral clavicle fractures. Researchers will monitor outcomes including the success rate of anesthesia during the operation, timing of first request for additional pain relief postoperatively, total opioid use, patient satisfaction, and any complications within 24 hours after surgery. The study will include adults aged 18 to 65 and last until July 2026, with data collected to compare the two anesthesia strategies.
CONDITIONS
Brief 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 of clavicle fractures.
You will not qualify if you...
- Coagulopathy.
- Infection at block site.
- Allergy to local anesthetics.
- Morbid obesity (body mass index >35 kg/m2).
- Pre-existing neurological disease.
- Difficult communication.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Surgical day
Participants receive anesthesia through Superficial Cervical Plexus Block combined with either Clavipectoral Fascial Plane Block or Interscalene Brachial Block during clavicle surgery.
1 visit (in-person)
Duration - 24 hours postoperatively
Participants are monitored postoperatively for pain management, rescue analgesia use, morphine consumption, patient satisfaction, and complications within 24 hours after surgery.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Tanta University
Tanta, El-Gharbia, Egypt, 31527
Actively Recruiting
Research Team
A
Ahmed M Aboeldahab, Master
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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