Comparative Study of Subcoracoid Tunnel Block Versus Costoclavicular Block

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age65-85
SponsorZagazig University

About this trial

The purpose of this study is to compare the analgesic outcomes (time to first analgesic request, total amount of analgesic consumption, and pain scores) following the ultrasound-guided subcoracoid tunnel block or costoclavicular block for elderly patients undergoing distal upper limb surgeries.

Eligibility criteria

Qualifiers

Patients acceptance to share in the study.

Patients with ASA physical status I-II.

Patients with a body mass index (BMI): of 18.5-30 kg/m2.

Patients undergoing distal upper limb surgeries not more than 2 hours.

Disqualifiers

Patients with a history of allergic reactions or contraindications to local anesthetics.

Patients with significant comorbidities (e.g., severe cardiovascular, neurological, or musculoskeletal disorders).

Patients with respiratory insufficiency.

Patients with coagulation disorders or taking drugs affecting surgical hemostasis.

Trial design

Treatments tested in this trial

  • subcoracoid tunnel block
  • Costoclavicular block

Treatment groups

70 Participants
are divided into 2 treatment groups

Sponsors and collaborators