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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05187988
Other study ID # Soh-Med-21-11-02
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 5, 2022
Est. completion date September 5, 2022

Study information

Verified date September 2022
Source Sohag University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this study investigators will compare two different approaches of brachial plexus block ;supraclavicular approach and retroclavicular approach regarding success rate, duration of block, complications


Recruitment information / eligibility

Status Completed
Enrollment 100
Est. completion date September 5, 2022
Est. primary completion date September 5, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - 100 patients doing distal arm surgery, elective , 18 to 60 years old , will be included in double blinded randomized study. Exclusion Criteria: - Patient refusal . - local infection or deformity at the block site. - Patient with significant neurological , psychiatric or neuromuscular disease. - Pregnancy or lactating women . - Coagulopathy . - Morbid obesity . - History of allergy to local anaesthetics

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
supraclavicular brachial plexus block
group will receive brachial plexus block above clavicle,Injection of anaesthetic will be done in brachial plexus around subclavian artery
Retroclavicular brachial plexus block
group will receive brachial plexus block inferior to the clavicle,injection of anaesthetic will be done around axillary artery

Locations

Country Name City State
Egypt Sohag University Hospital Sohag

Sponsors (1)

Lead Sponsor Collaborator
Sohag University

Country where clinical trial is conducted

Egypt, 

References & Publications (4)

Albrecht E, Mermoud J, Fournier N, Kern C, Kirkham KR. A systematic review of ultrasound-guided methods for brachial plexus blockade. Anaesthesia. 2016 Feb;71(2):213-27. doi: 10.1111/anae.13347. Epub 2015 Dec 16. Review. — View Citation

Charbonneau J, Fréchette Y, Sansoucy Y, Echave P. The Ultrasound-Guided Retroclavicular Block: A Prospective Feasibility Study. Reg Anesth Pain Med. 2015 Sep-Oct;40(5):605-9. doi: 10.1097/AAP.0000000000000284. — View Citation

Grape S, Pawa A, Weber E, Albrecht E. Retroclavicular vs supraclavicular brachial plexus block for distal upper limb surgery: a randomised, controlled, single-blinded trial. Br J Anaesth. 2019 Apr;122(4):518-524. doi: 10.1016/j.bja.2018.12.022. Epub 2019 Jan 31. — View Citation

Yazer MS, Finlayson RJ, Tran DQ. A randomized comparison between infraclavicular block and targeted intracluster injection supraclavicular block. Reg Anesth Pain Med. 2015 Jan-Feb;40(1):11-5. doi: 10.1097/AAP.0000000000000193. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Block success rate Investigator will compare success rate of both types of block and which one is more likely to be successfully administrated one year
Primary Complications Investigators will compare complications like pneumothorax,nerve injury,bleeding and which one is more likely to cause complications one year
Primary Duration of sensory and motor blockade Time which each procedure will take to block sensory and motor stimuli one year
Secondary Duration of procedure Time which took the investigator to administrate each type of block one year
Secondary Number of needle passes number of times in which needle has entered been entered into the participant in each group one year
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