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NCT00468390 Clinical Trial

Capsaicin-Evoked Pain in Patients With CRPS

CRPS (Complex Regional Pain Syndromes) Clinical Trial

Official title:
Capsaicin-Evoked Pain in Patients With Complex Regional Pain Syndrome

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00468390
Other study ID # Capsaicin in CRPS
Secondary ID
Status Completed
Phase N/A
First received May 1, 2007
Last updated October 10, 2008
Start date April 2007
Est. completion date January 2008

Study information
Verified date October 2008
Source Danish Pain Research Center
Contact n/a
Is FDA regulated No
Health authority Denmark: Danish Medicines Agency
Study type Observational

Clinical Trial Summary

To evaluate the effect of capsaicin in patients with Complex Regional Pain Syndrome.

Description:

Primary outcome parameters: Capsaicin-induced pain and inflammation.

Secondary outcome parameters: Peripheral sensory and autonomic function.

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date January 2008
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age: 18 or older.

- Pain in arm or hand > 3 months.

- Diagnosed with CRPS acc. to diagnostic research criteria (Harder et al., 2005)

- Inclusion of healthy subjects: age-, gender-, and BMI-matched.

Exclusion Criteria:

- Other significant disease affecting the parameters measured, including cardiovascular disease.

- Treatment with anticholinergics, sympathomimetics and parasympathomimetics, and alpha- and beta-adrenergics.

Study Design

Observational Model: Case Control, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
Denmark Danish Pain Research Center, Aarhus University Hospital Aarhus

Sponsors (1)
Lead Sponsor Collaborator
Danish Pain Research Center

Country where clinical trial is conducted

Denmark, 

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