Clinical Trials Directory

Trials / Completed

CompletedNCT01700634

fMRI Evaluation of Pain Central Sensitization Phenomena in Subjects With Knee Osteoarthritis

Status
Completed
Phase
Study type
Observational
Enrollment
90 (actual)
Sponsor
Parc de Salut Mar · Academic / Other
Sex
All
Age
45 Years
Healthy volunteers
Accepted

Summary

The aim of this project is to investigate fMRI ability to identify pain central sensitization in chronic knee OA. Patients with high and low central sensitization and healthy control subjects will be included. Central sensitization will be clinically defined based on the evidence of regional spread of pain (spreading sensitization) and increased pain response to repeated stimulation (temporal summation). Operatively, a patient will be assigned to high sensitization group when showing (i) clinical evidence of pain or altered sensations spread beyond the knee joint by manual palpation, (ii) a minimum of 3 anatomical sites around the knee showing a pressure pain threshold below 4 kg/cm2 (tender points), (iii) pain score of 4 points or more in a 11-point scale during 4 kg/cm2 pressure stimulation on the anterior/medial surface of the tibial bone (the site selected for the fMRI experiment) and (iv) increase of at least 1 point in a 11-point scale after 10 repeated pressure stimulation on the tenderest point around the knee. A three-step strategy is proposed to characterize the phenomenon by assessing (i) brain response to direct pressure stimulation on the painful knee, which will reflect the combination of peripheral and central sensitization; (ii) brain response to pressure stimulation on a non-arthritic hyperalgesic area (i.e., the anterior surface of the tibia), which will mostly reflect central sensitization mediated at the spinal cord level, and (iii) brain response to moderately painful heat stimulation on a healthy skin area (i.e., volar forearm), which will reflect central sensitization occurring in the brain and involving the highest-level pain modulatory mechanisms. An additional evaluation is proposed using resting-state fMRI to assess potential alterations in baseline brain functional organization.

Conditions

Timeline

Start date
2012-09-01
Primary completion
2014-07-01
Completion
2016-10-01
First posted
2012-10-04
Last updated
2016-10-05

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT01700634. Inclusion in this directory is not an endorsement.