Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
NOT YET RECRUITING
NCT07871994

Body Mass Index and Outcomes of Ultrasound-Guided Infraclavicular Brachial Plexus Block

Sponsor: Ankara City Hospital Bilkent

View on ClinicalTrials.gov

Summary

This study aims to investigate whether body mass index (BMI) is associated with differences in the time needed to perform an ultrasound-guided infraclavicular nerve block and how well the block works. This type of regional anesthesia involves injecting a local anesthetic near the nerves below the collarbone to numb the arm for surgery. The study will include 100 adults undergoing planned hand, wrist, or forearm surgery at Ankara Bilkent City Hospital. Researchers will compare 50 participants with a BMI below 30 kg/m² and 50 participants with a BMI of 30 kg/m² or higher. The study will assess the time needed to perform the block, block success, the time until sensation and movement are blocked, and patient satisfaction. Researchers will also examine whether arm circumference and muscle measurements are associated with block outcomes. This is an observational study. Participants will receive routine anesthesia and surgical care, and their treatment will not be assigned or changed for research purposes.

Official title: Effect of Body Mass Index on Infraclavicular Brachial Plexus Block Outcomes: A Comparison of Obese and Non-obese Patients

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

100

Start Date

2026-10-15

Completion Date

2027-04-15

Last Updated

2026-10-13

Healthy Volunteers

Yes

Interventions

PROCEDURE

Ultrasound-guided infraclavicular brachial plexus block

Ultrasound-guided infraclavicular brachial plexus block will be performed as part of routine anesthetic care for elective hand, wrist, or forearm surgery. Local anesthetic will be injected posterior to the axillary artery under ultrasound guidance, with intermittent aspiration. Sensory and motor block development will be assessed for 30 minutes after injection. The same block technique will be used in both BMI cohorts.