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NCT Number: NCT06831604

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

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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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Tanta University

Tanta, El-Gharbia, 31527, Egypt

Location status: Recruiting

Location contact

Ahmed M Aboeldahab, Master

CONTACT

[email protected]

00201069784512

Ahmed M Elsheikh, MD

SUB_INVESTIGATOR

Kamal E Haikal, MD

SUB_INVESTIGATOR

Mohamed S Abdelghany, MD

SUB_INVESTIGATOR

Mohammed S ElSharkawy, MD

SUB_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

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).

Other names: Group I

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

Drug

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

Other names: Group II

Primary outcomes

  1. Success rate

    Time frame: Intraoperatively

    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.

Secondary outcomes

  1. First request of the rescue analgesia

    Time frame: 24 hours postoperatively

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

  2. Total morphine consumption

    Time frame: 24 hours postoperatively

    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").

  3. Degree of patient satisfaction

    Time frame: 24 hours postoperatively

    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).

  4. Incidence of Complications

    Time frame: 24 hours postoperatively

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

Study contacts

Contact information is provided by the study sponsor or research team.

Ahmed M Aboeldahab, Master

CONTACT

[email protected]

00201069784512

Sponsors and collaborators

Lead sponsor

Tanta University

Other

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Feb 18, 2025
Registry last updated
Mar 11, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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