Parkinson's Disease Trial, Recruiting NCT05998772 Sponsor: University Hospital Schleswig-Holstein Condition: Parkinson's Disease
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Parkinson's Disease Trial, Recruiting

NCT05998772
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:

  • People who have been diagnosed with Parkinson's Disease at a moderate stage (Hoehn & Yahr stage 1.5 to 3)
  • People who are able to temporarily pause their Parkinson's medications in the morning without experiencing significant problems
  • People who are able to give informed consent, and who have sufficient mental clarity to do so (a short memory and thinking test score of 18 or above may be used to confirm this if there is any doubt)
  • People who are between 50 and 80 years old (a small number of exceptions outside this age range may be considered)
  • People who are willing to complete a 3-day food diary on one occasion, which helps the trial team place participants into one of two groups: those who experience increased cravings for sweet foods, and those who do not

Who may not be able to join:

  • People who have another significant neurological condition that primarily affects the brain or central nervous system (for example, multiple sclerosis)
  • People who have been diagnosed with diabetes or pre-diabetes
  • People who take medications that affect how the body processes blood sugar — this includes a wide range of medicines such as diabetes drugs, steroids (glucocorticoids), certain immunosuppressants, beta-blockers, certain water tablets, certain asthma medications, some antipsychotics, some antidepressants, some epilepsy medications, cholesterol-lowering drugs (statins), HIV medications, lithium, and others (confirm with trial site for the full list)
  • People who have a cardiac pacemaker or a brain stimulation device (brain pacemaker)

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 27 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: 004943150023983

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

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
University Hospital Schleswig-Holstein
Registry
ClinicalTrials.gov
Start date
1 September 2023
Est. completion
1 December 2025

Where this trial is recruiting

🇩🇪 Germany

Primary endpoints

Concentration of Insulin in µU/mL; Motor function; Concentration of Blood Glucose in mg/dL

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: 27 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