Status:
WITHDRAWN
Comparison of the Infraclavicular and Axillary Approaches for Continuous Ultrasound-guided Brachial Plexus Block.
Lead Sponsor:
University Hospital, Bordeaux
Conditions:
Anesthesia, Regional
Brachial Plexus Block
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
Prospective randomized study comparing the axillary and the infraclavicular approaches for continuous brachial plexus block after hand surgery.
Detailed Description
Regional anesthesia is considered as the gold standard for analgesia and anesthesia of hand surgeries. However, with a single-shot technique, a maximum of 13 hours of analgesia is obtained, even with ...
Eligibility Criteria
Inclusion
- Adult patients with a social insurance number
- ASA 1-3
- Patients undergoing hand surgery requiring a continuous brachial plexus block
- Elective or urgent surgery
- Effective contraception (HAS criteria)
- Informed consent
Exclusion
- Contraindication to the installation of a continuous brachial plexus block (coagulopathy, refusal, allergy to the medication)
- Preexisting neuropathy
- Pregnancy
- Arteriovenous fistula
- Obesity (BMI \>40)
- Another surgical site implicated during the surgery
- Incapacity to abduct the operated arm
- Preoperative use of morphine or equivalent
Key Trial Info
Start Date :
September 1 2019
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2020
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT04053491
Start Date
September 1 2019
End Date
October 1 2020
Last Update
March 17 2023
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