Status:

RECRUITING

Influence of Glucose on Metabolism and Clinical Symptoms of Patients With Parkinson's Disease

Lead Sponsor:

University Hospital Schleswig-Holstein

Collaborating Sponsors:

University of Kiel

Conditions:

Parkinson Disease

Nutritional and Metabolic Diseases

Eligibility:

All Genders

50-80 years

Brief Summary

Many patients with Parkinson's Disease (PD) report an increased consumption of fast-acting sugars. This tendency to consume sweet, high-sugar foods occurs in some patients even before the onset of car...

Eligibility Criteria

Inclusion

  • Diagnosis of Parkinson's Disease, stage Hoehn \& Yahr 1.5-3
  • Ability to pause antiparkinsonian medication in the morning without relevant impairment
  • Capacity to give consent (determined in doubt by two independent neurologists, MOCA ≥18) and written informed consent.
  • Patients are between 50 and 80 years of age, with exceptions for a maximum of 5 additional patients enrolled per group
  • For stratification into patients with and without sweet craving, a 3-day dietary protocol should be completed once by the patients
  • Group I: increased hunger for sweets.
  • Group II: no increased hunger for sweets.
  • For the stratification into patients with and without increased hunger for sweets, participants are asked to answer the following questions:
  • Do you have sudden attacks of cravings for sweets?
  • Would you say that your consumption of sweet food has increased in recent years?
  • Would you describe your consumption of sugary food as increased or excessive?
  • If one of the questions is answered with yes, participants will be assigned to group I, if all questions are answered with no, participants will be assigned to group II.

Exclusion

  • Other significant neurological diseases primarily affecting the central nervous system (e.g., multiple sclerosis)
  • Diagnosis of diabetes mellitus or prediabetes
  • Use of medications that affect glucose metabolism, such as antidiabetics, glucocorticoids, ciclosporin, tacrolimus, sirolimus, beta-blockers, thiazide diuretics, beta-2 adrenoreceptor agonists, theophylline, Clozapine, olanzapine, paliperidone, quetiapine, risperidone, tricyclic antidepressants, mirtazapine, mianserin, carbamazepine, gabapentin, pregabalin, valproic acid, lithium, antiretroviral drugs, statins
  • cardiac or brain pacemakers

Key Trial Info

Start Date :

September 1 2023

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

December 1 2025

Estimated Enrollment :

50 Patients enrolled

Trial Details

Trial ID

NCT05998772

Start Date

September 1 2023

End Date

December 1 2025

Last Update

September 22 2025

Active Locations (1)

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Department for Neurology, University of Kiel

Kiel, Germany, 24118