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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02138344
Other study ID # EK-04/2006 / PB_2016-02051
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date April 2006
Est. completion date December 2024

Study information

Verified date May 2024
Source University of Zurich
Contact Michèle Hubli
Phone +41 44 510 72 03
Email michele.hubli@balgrist.ch
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Development of neuropathic pain is one of the most disabling sequels after spinal cord injury (SCI) and in peripheral nerve diseases. The functionality of the pain pathway in humans as well as its plastic changes following SCI can be assessed in vivo by surface electrophysiological recordings and functional magnetic resonance imaging after noxious heat stimulation of the skin. Aims: a) establishing a clinically applicable assessment of the pain pathway and characterizing its changes as a consequence of SCI and in peripheral nerve diseases in an objective manner, b) characterizing plastic changes in the pain pathway in SCI patients with neuropathic pain and in patients with peripheral nerve diseases and relating them to the development of neuropathic pain syndromes.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date December 2024
Est. primary completion date December 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Uninjured - Scord injured subjects - Subjects with peripheral nerve diseases - Patients resident in Switzerland Exclusion Criteria: - Presence of any central psychiatric disorder (that precludes subject from giving informed and voluntary consent) - For fMRI measurements: "yes" for any item in the MR-risk questionnaire - Patients resident outside from Switzerland

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Switzerland Curt, Armin, MD Zurich

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pain, sensory and autonomic assessments 2 - 4 weeks