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Clinical Trials/EUCTR2008-008896-32-DE
EUCTR2008-008896-32-DE
Active, not recruiting
Phase 1

Memory, Ageing, and the Cholinergic Systema combined fMRI and PET study - MACS

niversity of Cologne0 sites42 target enrollmentJuly 21, 2009

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Patients with mild cognitive impairment (MCI) (50-80 years), who are at greater risk of developing alzheimer's dementia will be recruited in the present study and will be compared to an age-matched group of healthy subjects (50-80 years).
Sponsor
niversity of Cologne
Enrollment
42
Status
Active, not recruiting
Last Updated
5 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
July 21, 2009
End Date
May 7, 2014
Last Updated
5 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
niversity of Cologne

Eligibility Criteria

Inclusion Criteria

  • Healthy older subjects (aged 50\-80 years) with no neurological or psychiatric diseases and normal scores in neuropsychological tests (VLMT, MMSE, BDI, Digit Span und LPS4\).
  • Patients with MCI (aged 50\-80 years) without other neurological or psychiatric diseases. MCI will be defined as amnestic MCI with isolated memory deficits without significant effect on daily living.
  • VLMT scores \> 1,5 standard deviations below normal values, MMSE score \> 23, normal scores in BDI, Digit Span und LPS4, normal ADL scores,
  • Written and informed consent.
  • Normal neurological examination.
  • Normal body examination including auscultation of lung and heart as well as palpation of the abdomen.
  • Normal ECG.
  • Systolic blood pressure 100\-160 mmHg, diastolic blood pressure 50\-100 mmHg
  • heart frequency 50\-100\.
  • An equal number of men and women will be tested in order to draw valid inference from the study for the general population since it is estimated that MCI is represented in men and women to the same degree.

Exclusion Criteria

  • Neurologic or psychiatric diseases (other than MCI). Severe lung, liver, kidney or gastrointestinal tract diseases, cancer, thyreotoxicosis, drug hypersensitiviy for rivastigmine, history of contact dermatitis under transdermal rivastigmine therapy, pregnancy or breast\-feeding. Bronchial asthma, gangrene, coronary heart disease, bradycardia, cardiac arrhythmia, gastric ulcers, mechanical constipation, arterial hypotension. Medication with choline esterase inhibitors, epilepsy, arterial hypotension. Medication with anticholinergic drugs.
  • For the MRI part: Metal parts in or on body, tattoos, claustrophobia. With the exception of MR\-compatible implants in MCI\-patients.
  • PET\-investigation, healthy subjects: previous nuclear medicine investigations for research purposes. Hypersensitivity to MP4A.
  • PET\-investigation, MCI patients: previous nuclear medicine investigations for research purposes in the past 10 years, if an effective dose of 10 mSv is expected to be exceeded.

Outcomes

Primary Outcomes

Not specified

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