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UNKNOWNNCT02383134

Maximal Distance for Successful Supraclavicular Block

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 ...

Lead sponsor: Tunisian Military Hospital•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Tunisian Military Hospital

Age

18 - 85 years

Sex

ALL

Healthy Volunteers

No

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

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: May 13, 2015Terms

Trial snapshot

StatusUNKNOWN

Phase—

Enrollment44

Start dateMay 2015

Last updatedMay 13, 2015

Condition

Regional Anesthesia Ultrasound Supraclavicular Block

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: May 13, 2015Data synced to Clareo: May 25, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions