Development of Complex Regional Pain Syndrome (CRPS) Severity Score As A Clinical Tool To Monitor Disease Progressio

Recruiting

• Conditions: Dystrophy; Reflex Sympathetic Dystrophy; RSD; 10034606

• Registration Number: NL-OMON35516
• Lead Sponsor: eids Universitair Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

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

Inclusion Criteria

Subjects who are 18 years or older, who have the cognitive abilities to understand the demands of the study, who have sufficient command of Dutch and who meet the provisional 2011 IASP CRPS Clinical Diagnostic Criteria (Revised) are included in the study. .

Exclusion Criteria

Patients who do not meet the inclusion criteria, do not give informed consent and who have other conditions that may explain their signs and symptoms.

Study & Design

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

Primary Outcome Measures

Name	Time	Method
<p>The CRPS severity score is the primary study variable. The objective is to<br /><br>evaluate the test-retest reliablity and the responsiveness of this score. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Correlation of the change in the CRPS severity score with those of the changes<br /><br>in other instruments, such as pain intensity, other pain measures and the<br /><br>SF-36.</p><br>