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Completed

NCT Number: NCT05240729

Using Ultrasound in Infraclavicular in Upper Limb Surgeries

Comparison of 3 approach of infraclavicular brachial plexus

Completed

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Key information

Conditions

Upper Limb Surgeries

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Facutly of Medicine

Minya, 61111, Egypt

About this study

Comparison of retroclavicular & costoclavicular and classic type of infraclavicular brachial plexus block for upper limb surgeries

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age: between 18 and 60 years ASA I and II BMI between 18 and 35 surgeries to forearm and hand

Exclusion criteria

  • patient refusal pregnancy allergy to local anaesthetics local infection neuropathy ,coagulopathy anatomical abnormality in clavicular region

Treatment and study plan

Infraclavicular brachial plexus block

Procedure

Using ultrasound in 3different techniques of infraclavicular brachial plexus block

Primary outcomes

  1. Motor and sensory block success rate

    Time frame: 30 min

    Success rate 30 min after local anasthetic injections

Sponsors and collaborators

Lead sponsor

Minia University

Other

Registry information

Official study title

Ultrasound Guided Retroclavicular Approach Versus Costoclavicular Approach of Infraclavicular Brachial Plexus Block for Upper Limb Surgeries

Important dates

Study start
2021
Primary completion
2022
Study completion
2022
First posted
Feb 15, 2022
Registry last updated
Jan 10, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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