Clinical Trial

Comparison of Costoclavicular and Lateral Sagittal Infraclavicular Blocks

Study acronym: CCLS-ICB
Completed
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Summary
This randomized clinical study aims to compare the effects of two different ultrasound-guided infraclavicular brachial plexus block techniques-costoclavicular and lateral sagittal approaches-in patients undergoing forearm, wrist, or hand surgery. The primary objective of the study is to evaluate and compare the incidence of hemidiaphragmatic dysfunction associated with these two block techniques. Secondary outcomes include sensory and motor block characteristics, postoperative pain scores, analgesic requirements, and potential block-related complications. Eligible adult patients scheduled for elective forearm or hand surgery are randomly assigned to receive either a costoclavicular or a lateral sagittal infraclavicular nerve block using bupivacaine under ultrasound guidance. Standard general anesthesia and postoperative analgesia protocols are applied. The results of this study are expected to provide evidence on the relative safety and efficacy of these two infraclavicular block approaches, particularly regarding diaphragmatic function, and to help guide anesthesiologists in selecting the most appropriate regional anesthesia technique for upper extremity surgery.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-01-28.
Trial Details
NCT Number NCT07386470
Lead Sponsor Gazi University
Conditions Hemidiaphragmatic Paralysis, Upper Extremity Surgery
Enrollment 91 participants
Start Date 2022-10-15
Primary Completion 2023-04-15 (estimated)
Study Completion 2023-04-15 (estimated)
Updated on ClinicalTrials.gov 2026-02-05