CCLS-ICBComparative Study on Hemidiaphragmatic Function: Costoclavicular vs. Lateral Sagittal Infraclavicular Block
This study compares the impact of two different block techniques, costoclavicular and lateral sagittal infraclavicular, on the movement of your diaphragm during normal and deep breathing, as measured by ultrasound.
Ultrasound-guided Infraclavicular block
Treatment Study
Summary
Study start date: October 15, 2022
Actual date on which the first participant was enrolled.This study focuses on comparing two different ultrasound-guided techniques for infraclavicular brachial plexus block, which are used to numb the arm for forearm, wrist, or hand surgery. The techniques are called costoclavicular and lateral sagittal approaches. The study is particularly interested in how these techniques affect the movement of half of the diaphragm, a muscle that helps us breathe. Adults scheduled for elective forearm or hand surgery are invited to participate in this study, which aims to improve the safety and effectiveness of regional anesthesia for upper extremity surgery. Participants in this study will receive either a costoclavicular or a lateral sagittal infraclavicular nerve block using a medication called bupivacaine, under ultrasound guidance. The study measures the movement of the diaphragm during normal and deep breathing using ultrasound to assess the effect of these block techniques. Other aspects evaluated include sensory and motor block characteristics, pain scores after surgery, pain medication requirements, and potential complications related to the block. The results of this study will help guide anesthesiologists in choosing the most appropriate technique for upper extremity surgery.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.91 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 80 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Inclusion Criteria: * Adults aged 18-80 years * ASA physical status I-III * Scheduled for forearm, wrist, or hand surgery * Planned infraclavicular brachial plexus block Exclusion Criteria: * Refusal of regional anesthesia * Known allergy to local anesthetics * Infection at the block site * Pre-existing neurological deficit in the operative limb * Severe pulmonary disease * Coagulopathy or sepsis * BMI \> 40 kg/m² * Psychiatric disorders
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Gazi University Faculty of Medicine, Department of Anesthesiology and Reanimation
Ankara, Turkey (Türkiye)Open Gazi University Faculty of Medicine, Department of Anesthesiology and Reanimation in Google Maps