RecruitingNot ApplicableNCT06008704

Pain in Parkinson's Disease: Exploration of the Serotonin System in Positron Emission Tomography (PET [18F]-MPPF)

Pathophysiology of Pain in Parkinson's Disease: Exploration of the Serotonin System in Positron Emission Tomography (PET [18F]-MPPF)


Sponsor

University Hospital, Toulouse

Enrollment

34 participants

Start Date

Jan 1, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This project will explore the involvement of the serotonin system in the pathophysiology of PD-related central pain. Thus, the serotonin system will be evaluated in PD patients with and without central pain who will benefit from brain positron emission tomography (PET) allowing in vivo imaging of 5HT1A receptors and multimodal brain MRI including morphometric imaging and functional connectivity (resting state acquisition).


Eligibility

Min Age: 40 YearsMax Age: 80 Years

Plain Language Summary

Simplified for easier understanding

This study is investigating whether changes in the brain's serotonin system (a chemical messenger) might explain why some Parkinson's disease patients experience chronic pain. Researchers will use a special type of brain scan (PET scan) to compare brain activity in Parkinson's patients with and without pain. **You may be eligible if...** - You have a confirmed diagnosis of Parkinson's disease - You have been on a stable Parkinson's medication regimen for at least 4 weeks - You score above 25 on a standard memory and thinking test (MoCA) - You have mild-to-moderate depression (HADS-D score ≥11) - If enrolling in the "pain" group: you have chronic central pain related to Parkinson's for at least 3 months, rated at least 4/10 in severity - If enrolling in the "no pain" group: your pain is 4/10 or less and does not interfere with daily life **You may NOT be eligible if...** - You are receiving second-line Parkinson's therapy - You have a significant psychiatric history - You take medications that interact with serotonin receptors (5HT1A) - You have a contraindication to MRI (e.g., metal implants) - You have severe involuntary movements (dyskinesias) that would interfere with the scan Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIAGNOSTIC_TESTClinical assessment

The clinical assessment consists on behavioural and motor evaluations to determine the characteristics of the population

DIAGNOSTIC_TESTPain characteristics assessment

The pain characteristics assessment will be made with a variety of scales and questionnaires which allow to identify the extent of central pain and functional impairment

DIAGNOSTIC_TESTMRI

The MRI examination allows anatomical imaging, diffusion imaging and functional imaging to measure specific markers

DIAGNOSTIC_TESTThermotest

The thermotest is performed to assess the pain perception threshold

DIAGNOSTIC_TESTUPDRS-III Scale

The UPDRS-III scale allows to asses motor functionality of PD patients

DIAGNOSTIC_TEST[18F]-MPPF PET scan

The PET scan after injection of \[18F\]-MPPF at a dose of 200 Megabecquerel/kg +/-10% allows in vivo imaging of 5HT1A receptors


Locations(1)

Centre Hospitalier Universitaire de Toulouse

Toulouse, Haute-Garonne, France

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NCT06008704


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