RecruitingNot ApplicableNCT06831604

Superficial Cervical Plexus Block With Either Clavipectoral Fascial Plane Block or Interscalene Brachial Block for Clavicle Surgeries Anesthesia

Ultrasound Guided Superficial Cervical Plexus Block With Either Clavipectoral Fascial Plane Block or Interscalene Brachial Block for Clavicle Surgeries Anesthesia: A Randomized Controlled Trial


Sponsor

Tanta University

Enrollment

60 participants

Start Date

Feb 20, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Superficial Cervical Plexus Block (SCPB) and Clavipectoral Fascial Plane Block (CPB) and a drug called Superficial Cervical Plexus Block (SCPB) and Interscalene Brachial Block (ISBP) for people with clavicle surgeries, clavipectoral fascial plane block, and other related conditions. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 65 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGSuperficial Cervical Plexus Block (SCPB) and Clavipectoral Fascial Plane Block (CPB)

Patients will receive Superficial Cervical Plexus Block (SCPB) and Clavipectoral Fascial Plane Block (CPB).

DRUGSuperficial Cervical Plexus Block (SCPB) and Interscalene Brachial Block (ISBP)

Patients will receive Superficial Cervical Plexus Block (SCPB) and Interscalene Brachial Block (ISBP)


Locations(1)

Tanta University

Tanta, El-Gharbia, Egypt

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NCT06831604


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