Comparing two anesthesia techniques for clavicle surgeries

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study evaluates the effectiveness and safety of ultrasound-guided superficial cervical plexus block (SCPB) combined with either clavipectoral fascial plane block (CPB) or interscalene brachial plexus block (ISBP) for anesthesia during clavicle surgeries. Clavicle surgeries often require precise pain control due to the common occurrence of fractures and dislocations in this area. The SCPB provides sensory anesthesia to the cervical and upper thoracic regions, while the ISBP offers comprehensive analgesia for the shoulder and upper arm. The CPB is a newer technique aimed at enhancing postoperative analgesia for clavicular procedures.

Why it matters

Who can join: the full rules

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.

Where it's running

• Tanta University
  Tanta, El-Gharbia, Egypt Recruiting

Study contacts

• Study coordinator: Ahmed M Aboeldahab, Master
• Email: ahmed.aboeldahab1422@gmail.com
• Phone: 00201069784512

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.