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Maximal Distance for Successful Supraclavicular Block

T

Tunisian Military Hospital

Status

Unknown

Conditions

Supraclavicular Block
Ultrasound
Regional Anesthesia

Study type

Observational

Funder types

Other

Identifiers

NCT02383134
TunisianMH

Details and patient eligibility

About

The achievement of peripheral nerve block requires several needle passes, with each of them being at risk of causing nerve injury either by direct trauma or intraneural injection even with the use of the ultrasound.

The ultrasound guided supraclavicular brachial plexus block is known to be at risk of pneumothorax and / or nerve injury.

This study is designed to determine the maximal effective distance away from the nerve for the injection to be effective.

Enrollment

44 estimated patients

Sex

All

Ages

18 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ASA physical status I-III
  • 18-85 years of age, inclusive
  • surgery less than 3 hours

Exclusion criteria

  • contraindications to brachial plexus block (e.g., allergy to local anesthetics, coagulopathy, malignancy or infection in the area)
  • existing neurological deficit in the area to be blocked
  • pregnancy
  • history of neck surgery or radiotherapy
  • inability to understand the informed consent and demands of the study

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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