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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-02-20

Study Completion Date

2026-07-01

Brief Summary

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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.

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Detailed Description

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Clavicular fracture is the most common injury in the shoulder, it occurs in 35% of shoulder girdle fractures. Clavicle surgeries often involve addressing fractures, dislocations, or corrective procedures, and they generally require precise and effective pain control.

Traditional superficial cervical plexus block (SCPB) combined with interscalene brachial plexus block (ISBP) can be used in the operation of clavicle fracture.

The SCPB targets the cervical plexus, providing sensory anesthesia to the skin overlying the cervical and upper thoracic regions. It is often used in conjunction with other blocks to enhance analgesia in the upper shoulder and clavicle area.

The ISBP block involves the administration of local anesthetic at the level of the brachial plexus, typically performed between the anterior and middle scalene muscles. This approach provides comprehensive analgesia for the shoulder, upper arm, and part of the clavicular area.

Clavipectoral fascial plane block (CPB) is a new regional nerve block and can be used in anesthesia and postoperative analgesia for clavicle fracture surgery. CPB provides analgesia to the clavicular region and the upper shoulder.

Conditions

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Ultrasound Superficial Cervical Plexus Block Clavipectoral Fascial Plane Block Interscalene Brachial Block Clavicle Surgeries

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Group I

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

Group Type EXPERIMENTAL

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

Intervention Type DRUG

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

Group II

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

Group Type EXPERIMENTAL

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

Intervention Type DRUG

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

Interventions

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

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

Intervention Type DRUG

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

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

Intervention Type DRUG

Other Intervention Names

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Group I Group II

Eligibility Criteria

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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.

Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No