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Efficacy of Fish Oil Supplementation on Cognition in MCI Patients and the Influence of the APOE4 Allele

Not Applicable
Completed
Conditions
Mild Cognitive Impairment
Interventions
Dietary Supplement: fish oil
Dietary Supplement: placebo, sunflower oil
Registration Number
NCT00746005
Lead Sponsor
Wageningen University
Brief Summary

To study the short term effects of a pharmacological dose of fish oil on cognitive performance and on cerebral blood flow. Furthermore, we want to investigate whether carriers of the APOEε4 allele respond differently to fish oil treatment compared to non-carriers.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
40
Inclusion Criteria
  • Men and women
  • Diagnosed as having amnestic MCI: based on specific memory disturbances (cut-off of 1 sd, single or multiple domain amnestic MCI, according to Busse A et al37)
  • Presence of a principal caregiver willing to assist for a successful participation
  • Informed consent signed
Exclusion Criteria
  • Current or recent (<4 weeks) use of fish oil supplements
  • Consumption of fish more than 2 times/week
  • Current use of dementia (Alzheimer) medication
  • Current use of acenocoumarol or other anti-thrombotic drugs (because of the high dose of fish oil)
  • Serious liver disease
  • Use of more than 4 glasses of alcohol per day
  • Unable to participate as judged by the responsible medical physician
  • Allergy to fish(oil)
  • Swallowing problems
  • Participation in another clinical trial less than 2 months before the start of the trial or at the same time

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
1fish oil3 g EPA-DHA
2placebo, sunflower oilPlacebo: sunflower oil
Primary Outcome Measures
NameTimeMethod
cognitive performancebaseline and after 4 weeks
Secondary Outcome Measures
NameTimeMethod
blood flow-velocity in the middle cerebral arteries (assessed with TCD) and cortical tissue oxygenation, cerebral autoregulation, cerebral blood volume (assessed with NIRSbaseline and after 4 weeks

Trial Locations

Locations (2)

Radboud University Medical Center

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Nijmegen, Gelderland, Netherlands

Ziekenhuis Gelderse Vallei

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Ede, Gelderland, Netherlands

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