The effect of local anesthetic volume on the duration of single shot axillary brachial plexus block.

Completed

• Conditions: hand; wrist or forearm orthopaedic surgery; 10005944

• Registration Number: NL-OMON34121
• Lead Sponsor: Sint Maartenskliniek

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 11 June 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 30

Inclusion Criteria

- Patients, 18 years or older
- Body weight over 50 kg
- ASA classification I - III
- Patients undergoing single shot axillary brachial plexus block for hand, wrist or forearm orthopaedic surgery
- Written informed consent

Exclusion Criteria

- Contra-indications for regional anesthesia
- Known hypersensitivity to amide-type local anesthetics
- Known history of peripheral neuropathy

Study & Design

• Study Type: Observational non invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Duration of sensory AXB; time to (slight feeling and) full recovery<br /><br>Duration of motor AXB; time to (slight movement and) full recovery</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Proportion of patients with complete sensory and motor block 30 min after<br /><br>injection<br /><br>Efficacy of AXB<br /><br>Time to first demand for analgesic medication</p><br>