A Randomized Comparison Between Conventional and Costoclavicular Ultrasound-Guided Infraclavicular Blocks

Phase 2

Completed

• Conditions: Regional anesthesiaInfraclavicular brachial plexus block; Anesthesia; Analgesia

• Registration Number: TCTR20160525001
• Lead Sponsor: one

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2016-05-25
• Study Completion: 2016-09-30
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

- Patients undergoing upper extremity surgery (elbow and below).
- American Society of Anesthesiologists classification 1-3
- Body mass index between 18 and 30 kg/m2

Exclusion Criteria

- pre existing neuropathy or coagulopathy
- renal failure or hepatic failure
- allergy to local anesthetics
- pregnancy
- prior surgery in the area of the infraclavicular fossa
- chronic pain syndromes requiring opioid intake at home

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Onset time within 30 minutes after the end of the procedure Record the time from the end of local anesthetic drug injection to successful brachial plexus block

Secondary Outcome Measures

Name	Time	Method
Performance time within 20 minutes after starting the procedure Record the time from applying ultrasound probe on skin to the end of local anesthetic drug injection,Total anesthesia-related time (sum of performance and onset times) within 30 minutes after the end of the procedure Record the time from applying ultrasound probe on skin until successful brachi plexus block achieved,Complications within 60 minutes after the end of the procedure Record incidences of intravascular injection, systemic toxic, pneumothorax, diaphragm paralysis.,Number of needle passes during the procedure Record number of needle passes used to reach the target,Procedural discomfort at the end of the procedure Use visual analog scale from 0 to 10