Health Trials

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

ConditionsUltrasoundSuperficial Cervical Plexus BlockClavipectoral Fascial Plane BlockInterscalene Brachial BlockClavicle Surgeries
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorTanta University

About this trial

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 criteria

Qualifiers

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.

Disqualifiers

Coagulopathy.

Patients with infection at block site.

Allergy to local anesthetics.

Patient with morbid obesity (body mass index >35 kg/m2).

Trial design

Treatments tested in this trial

  • Superficial Cervical Plexus Block (SCPB) and Clavipectoral Fascial Plane Block (CPB)
  • Superficial Cervical Plexus Block (SCPB) and Interscalene Brachial Block (ISBP)

Treatment groups

60 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Tanta University

Lead sponsor

Source ClinicalTrials.gov