Parkinson's Disease Trial, Recruiting NCT06834191 Sponsor: Medical University of Warsaw Condition: Parkinson's Disease
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Parkinson's Disease Trial, Recruiting

NCT06834191
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

For the main study group (people with Parkinson's who take immune-suppressing medication):

  • People who have been diagnosed with Parkinson's disease according to recognised international diagnostic guidelines
  • People who have been regularly taking immune-suppressing medication (at the correct dose and on a consistent schedule for the condition it is treating) for more than 12 months, taken by mouth, injection, or inhalation
  • People who are willing and able to give formal consent to take part in the study

For the comparison group (people with Parkinson's who do not take immune-suppressing medication):

  • People who have been diagnosed with Parkinson's disease according to recognised international diagnostic guidelines
  • People who have no history of regularly taking immune-suppressing medications
  • People who are willing and able to give formal consent to take part in the study

Who may not be able to join:

For the main study group:

  • People who only take immune-suppressing medication occasionally or as needed, rather than on a regular, consistent schedule
  • People who have been taking immune-suppressing medication for less than 12 months
  • People whose underlying condition requiring immune-suppressing medication has not improved or has continued to worsen despite treatment

For both groups:

  • People with advanced cancer, severe heart failure, severe kidney failure, an untreated autoimmune disease, active inflammation, or a condition that affects how the body absorbs or processes medication
  • People who have dementia
  • People who are unable to give formal consent to participate

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 23 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: +48223265427

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Medical University of Warsaw
Registry
ClinicalTrials.gov
Start date
1 March 2025
Est. completion
1 December 2027

Where this trial is recruiting

🇵🇱 Poland

Primary endpoints

Annual motor progression rate - Unified Parkinson's Disease Rating Scale PART III OFF; Annual LEDD increase rate; Age of motor symptom onset

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov