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

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

This trial does not accept healthy volunteers

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

Design model

Parallel

Treatments tested in this trial

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

    Drug

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

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

    Drug

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

Treatment groups

60 Participants
are divided into 2 treatment groups
Group A: Group IExperimental treatment 1 intervention
Group B: Group IIExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Success rate

The block will be considered successful when complete sensory block is achieved within 45 min after injection of the study drug and inadequate block will be converted to general anesthesia and excluded from the study.

Time frame
Intraoperatively

Secondary outcomes

1

First request of the rescue analgesia

First request of the rescue analgesia will be recorded from the end of surgery till first dose of morphine administrated

Time frame
24 hours postoperatively
2

Total morphine consumption

Rescue analgesia of morphine will be given as 2 mg bolus if the visual Analogue Scale (VAS)\> 3 to be repeated after 30 min if pain persists until the VAS \< 4. Each patient will be instructed about postoperative pain assessment with VAS. VAS (0 represents "no pain" while 10 represents "the worst pain imaginable").

Time frame
24 hours postoperatively
3

Degree of patient satisfaction

The degree of patient satisfaction will be assessed on a 5-point Likert scale patient satisfaction (1, extremely dissatisfied; 2, unsatisfied; 3, neutral; 4, satisfied; 5, extremely satisfied).

Time frame
24 hours postoperatively
4

Incidence of Complications

Incidence of complications as local anesthetic systemic toxicity, nerve injury, diaphragmatic paresis, pneumothorax and high epidural block.

Time frame
24 hours postoperatively

Other outcomes

Sponsors and contacts

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