ltrasound guided fascia iliaca block: a comparison with the landmark method

Phase 4

Withdrawn

• Conditions: analgesie; pain management

• Registration Number: NL-OMON45479
• Lead Sponsor: Isala Klinieken

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 28 February 2024

Recruitment & Eligibility

• Status: Withdrawn
• Sex: Not specified
• Target Recruitment: 100

Inclusion Criteria

- Adults
- Hip fracture

Exclusion Criteria

- Allergy for levobupivacaïne
- Infection at injection site
- INR > 1,5
- Previous femoral vascular surgery at fracture site
- Non-cooperative patient and reduced level of consciousness

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Reduction in pain during immobilisation by using the visual analogue scale 60<br /><br>minutes after block placement. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>- Accordance between preceived block and guessed block by the patient<br /><br>- Time of maximum pain reduction after block placement<br /><br>- De difference in VAS reduction during dynamic and static exam after block<br /><br>placement<br /><br>- Side effects of the fascia iliaca compartment block (infection, hematoma,<br /><br>sensibility disorder, allergic reactions)</p><br>