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Clinical Trials/NL-OMON43432
NL-OMON43432
Withdrawn
Not Applicable

Aging-related memory impairment: a behavior-genomics study - Memory genomics

Takeda0 sites220 target enrollmentTBD
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ConditionsNo disorder: Age-related memory performance10042258

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
No disorder: Age-related memory performance
Sponsor
Takeda
Enrollment
220
Status
Withdrawn
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational invasive

Investigators

Sponsor
Takeda

Eligibility Criteria

Inclusion Criteria

  • •1\. The subject has to sign and date a written informed consent form prior to the initiation of study procedures;
  • •2\. The subject falls in the age\-range of one the cohorts, i.e. 18\-30; 40\-60; 60\-80;
  • •3\. The subject has good comprehension of the Dutch language
  • •4\. Normal memory performance

Exclusion Criteria

  • •\- Suffering from uncontrolled, clinically significant neurologic disease or other abnormality which may impact the ability of the subject to participate or potentially confound the study results, which includes pregnancy and having received chemo treatment during the past year.
  • •\- The presence of psychiatric illness including schizophrenia, depression, bipolar disorder, Attention Deficit Hyperactivity Disorder and autism;
  • •\- Smoking more than 10 cigarettes a day.
  • •\- Excessive drinking, i.e. \>20 glasses of alcohol containing beverages a week,
  • •\- Current use of psychoactive medication (e.g. antidepressants, antipsychotics), centrally acting beta blockers, use of recreational drugs from 2 weeks before until the end of the
  • •yearly testing ,
  • •\- Any sensory or motor deficits which could reasonably be expected to affect test performance.
  • •\- Consultation of a clinical expert for memory problems before having entered the study
  • •\- Having received any investigational compound within 60 days prior to the Baseline
  • •(Screening) Visit

Outcomes

Primary Outcomes

Not specified

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