Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
69 participants
OBSERVATIONAL
2018-01-01
2020-01-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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Dementia
Dementia
Tear sampling
Tear sampling using Schirmer's strips
MCI
Mild cognitive impairment
Tear sampling
Tear sampling using Schirmer's strips
SCD
Subjective cognitive decline
Tear sampling
Tear sampling using Schirmer's strips
HC
Cognitively healthy control
Tear sampling
Tear sampling using Schirmer's strips
Interventions
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Tear sampling
Tear sampling using Schirmer's strips
Eligibility Criteria
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Inclusion Criteria
* . Inclusion criteria were an MMSE score ≥ 20 and a CDR score from 0 to 1, thereby including patients across the whole clinical spectrum (i.e. from subjective cognitive disorder to (mild) dementia).
Exclusion Criteria:
* Exclusion criteria at baseline were neurological diseases (such as Normal Pressure Hydrocephalus, Morbus Huntington, brain tumor, epilepsy, encephalitis, recent Transient Ischemic Attack (TIA) or cerebrovascular accident (CVA) (\< 2 years), or TIA/CVA with concurrent (within three months) cognitive decline) and a history of psychiatric disorders (such as schizophrenia, bipolar disorder or psychotic problems, current major depressive disorder (within 12 months), or alcohol abuse).
ALL
Yes
Sponsors
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Maastricht University Medical Center
OTHER
Responsible Party
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Locations
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Academic Hospital Maastricht
Maastricht, , Netherlands
Countries
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Other Identifiers
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15-4-100
Identifier Type: -
Identifier Source: org_study_id