CRPS Multi site Validation Study: - Interobserver reliability using the Budapest criteria

• Conditions: Chronische Pijn; Complex Regional Pain syndrome; Reflex Sympathetic Dystrophy; 10029305

• Registration Number: NL-OMON31916
• Lead Sponsor: Vrije Universiteit Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 13 May 2024

Recruitment & Eligibility

• Status: Pending
• Sex: Not specified
• Target Recruitment: 50

Inclusion Criteria

CRPS patients of 18 years or older meeting the current criteria for CRPS

Exclusion Criteria

Patients with other complaints or syndromes that could otherwise account for the degree of pain and dysfunction

Study & Design

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

Primary Outcome Measures

Name	Time	Method
<p>Occurrence of signs and symptoms of CRPS</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Pain questionnaire (McGill pain questionnaire), quality of life, sensory<br /><br>assessment.</p><br>