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

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

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON35516
Enrollment
50
Registered
2011-11-28
Start date
2012-07-30
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dystrophy Reflex Sympathetic Dystrophy RSD

Interventions

None listed

Sponsors

Leids Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
The CRPS severity score is the primary study variable. The objective is to evaluate the test-retest reliablity and the responsiveness of this score.

Secondary

MeasureTime frame
Correlation of the change in the CRPS severity score with those of the changes in other instruments, such as pain intensity, other pain measures and the SF-36.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)