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

Launched by TANTA UNIVERSITY · Feb 17, 2025

Keywords

ClinConnect Summary

This clinical trial is studying different ways to provide anesthesia for patients undergoing clavicle surgeries. Researchers want to compare two specific techniques—the clavipectoral fascial plane block (CPB) and the interscalene brachial plexus block (ISBP)—with a method called the superficial cervical plexus block (SCPB). The goal is to find out which technique is more effective and safe for managing pain during and after these surgeries.

To participate in this trial, you need to be between 18 and 65 years old and have a specific type of clavicle fracture that requires surgery. You should also be in good health overall, based on a standard assessment used by anesthesiologists. However, if you have certain health conditions, such as bleeding disorders or allergies to local anesthetics, or if you find it difficult to communicate, you may not be eligible. If you join this study, you can expect to receive one of the anesthesia techniques and be monitored closely to ensure your safety and comfort throughout the process.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • Aged 18 to 65 years.
• • Both sexes.
• • American Society of Anesthesiologists (ASA) physical status I, II.
• • Patients with unilateral clavicular fractures undergo elective internal fixation of clavicle fractures.
• Exclusion Criteria:
• • Coagulopathy.
• • Patients with infection at block site.
• • Allergy to local anesthetics.
• • Patient with morbid obesity (body mass index \>35 kg/m2).
• • Pre-existing neurological disease.
• • Difficult communication.