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Comparison of Quality of Supraclavicular, Infraclavicular and Axillary Approach of Ultrasound-guided Brachial Plexus Block

H

Hillel Yaffe Medical Center

Status

Completed

Conditions

Pain

Treatments

Drug: Bupivacaine

Study type

Interventional

Funder types

Other

Identifiers

NCT01442558
0081-2011-HYMC

Details and patient eligibility

About

The aim of this study is to compare the quality of 3 methods of ultrasound-guided brachial plexus blocks for surgical anesthesia

Enrollment

101 patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA I-III physical status
  • Surgery of distal arm, forearm or hand

Exclusion criteria

  • Skin infection near block injection site
  • Allergy to local anesthetics
  • Peripheral neuropathy upper limb
  • INR of more than 1.4
  • Thrombocytopenia
  • Opioid dependency
  • Chronic pain syndrome
  • Lack of orientation to person, place and time
  • Patient refusal

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Single Group Assignment

Masking

Double Blind

101 participants in 3 patient groups

SCL
Active Comparator group
Description:
Supraclavicular ultrasound-guided brachial plexus block
Treatment:
Drug: Bupivacaine
ICL
Active Comparator group
Description:
Infraclavicular ultrasound-guided brachial plexus block
Treatment:
Drug: Bupivacaine
AX
Active Comparator group
Description:
Axillary ultrasound-guided brachial plexus block
Treatment:
Drug: Bupivacaine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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