Symptomatic Treatment of Vascular Cognitive Impairment
Launched by AMSTERDAM UMC, LOCATION VUMC · Mar 25, 2014
Trial Information
Current as of October 24, 2025
Unknown status
Keywords
ClinConnect Summary
Vascular Cognitive Impairment is an important cause of cognitive impairment and dementia. Till now, there are no approved symptomatic treatments for Vascular Cognitive Impairment. Research on novel pharmacological treatments that may reduce clinical symptoms in these patients is needed. Evidence suggests that executive dysfunction and memory impairment in Vascular Cognitive Impairment are caused by damage to monoaminergic and cholinergic neurotransmitter-systems, respectively.
However, patients with Vascular Cognitive Impairment form a clinically heterogeneous group, i.e. the extent to whi...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Outpatients
- • Objective executive dysfunction and/or memory impairment on neuropsychological tests and imaging evidence of cerebrovascular disease (white matter changes (Fazekas ≥2, (lacunar) infarcts)
- • Mini Mental State Examination (MMSE) ≥16
- • Clinical Dementia Rating Score (CDR of 0.5-1)
- • No contraindication for treatment with a Cholinesterase inhibitor (CEI) or Methylphenidate (MPH) (www.fk.cvz.nl)
- • Assessed by the treating neurologist as mentally capable of understanding the implications of study participation
- • Presence of an informant/caregiver at the information visit, signing of informed consent, and all study visits
- Exclusion Criteria:
- • Clinically relevant history of abnormal physical or mental health interfering with the study as determined by medical history taking and physical examinations obtained during the screening visit and/or at the study day as judged by the investigator;
- • Clinically relevant abnormal laboratory results, electrocardiogram (ECG) and vital signs, or physical findings at screening and/or at the start of the study day (as judged by the investigator);
- • Unwilling to or unable to stop smoking on the study day until the end of the study day
- • Other causes that can explain cognitive symptoms including but not limited to: delirium, multiple sclerosis, amyotrophic lateral sclerosis, progressive supranuclear palsy, mental retardation, infectious encephalitis that led to persistent cognitive deficits or head trauma with loss of consciousness that led to persistent cognitive deficits
- • Use of neuroleptics
- • Use of celiprolol or sotalol
- • Use of MAO-A/B inhibitors
- • Current use of centrally acting anticholinergics (e.g. oxybutynin, mebeverine, ipratropium(bromide))
- • Use of benzodiazepine within 48 hours before a study day
- • Current use of a CEI (rivastigmine, galantamine, donepezil)
- • Alcohol abuse (defined as use of alcohol despite significant areas of dysfunction, evidence of physical dependence, and/or related hardship due to alcohol)
- • Use of recreational drugs
- • Concomitant use of inhibitors of CYP2D6 (a/o kinidine, paroxetine, fluoxetine) or of CYP3A4 (a/o ketoconazole, ritonavir); unless patients are on a stable dose without any recent or upcoming changes
- • Any other condition that in the opinion of the investigator would complicate or compromise the study, or the well being of the subject.
- • Any contra-indication for MRI
About Amsterdam Umc, Location Vumc
Amsterdam UMC, located at VU Medical Center (VUmc), is a leading academic medical center in the Netherlands dedicated to advancing healthcare through innovative research and clinical trials. With a strong emphasis on translating scientific discoveries into practical applications, Amsterdam UMC collaborates closely with researchers, healthcare professionals, and industry partners to enhance patient outcomes. The institution is committed to rigorous ethical standards and regulatory compliance, ensuring the integrity and reliability of its clinical research initiatives across various medical disciplines.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Amsterdam, Netherlands
Patients applied
Trial Officials
Niels D Prins, MD, PhD
Principal Investigator
VUmc
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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