CompletedNot Applicable

Structural and Functional Grey and White Matter Changes in Patients With Pain Disorders

Switzerland82 participantsStarted 2015-05-04

Plain-language summary

The goal of this observational study is to examine the association between exact lesion location and presence of thalamic CPSP (Central post-stroke pain) in a larger number of patients after thalamic stroke.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

✓. Patients with thalamic central post-stroke pain (CPSP) :
✓. Patients with thalamic stroke without CPSP:
✓. Patients with migraine (other pain condition):
✓. Healthy controls:

What they're measuring

The exact lesion location in the thalamus in patients with thalamic pain compared to patients with thalamic stroke without pain

Timeframe: One time assessment with a duration of max. 90 minutes.

Trial details

NCT IDNCT05679297

SponsorUniversity Hospital, Basel, Switzerland

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2024-12-27

View on ClinicalTrials.gov More Central Post-stroke Pain trials