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Recruiting Phase 3 NCT04570085

Effect of CAFfeine on Cognition in Alzheimer's Disease

Phase 3 – large-scale trial before approval
Conditions: Alzheimer Disease

Sponsor: University Hospital, Lille

trial.available_in: БГ
Overview
Sporadic Alzheimer's disease is a multifactorial illness arising a major medico-economic stakes for our aging societies. There is currently no curative treatment available. Coffee is a complex beverage with psychostimulant properties whose main effective element, caffeine, has a pleiotropic effect on the central nervous system. Caffeine pharmacological properties enable its use like an Alzheimer's disease symptomatic treatment. Its supposed benefits mustn't obscure anxiety and insomnia caffeine effect at large dose, which Alzheimer's patients might be more vulnerable. The main study objective is to evaluate placebo-controlled caffeine efficacy (30 treatments weeks) on cognitive decline in Alzheimer's disease dementia at beginning to moderate stage (MMSE 16-24).
Who can participate
Inclusion Criteria: * Age ≥ 50 at screening * Probable Alzheimer dementia according to the criteria of the National Institute on Aging-Alzheimer's Association; diagnosis must be supported by brain imaging (CT or MRI) and blood test (including ionogram, kidney and liver function, calcemia, CRP, TSH, B12 vitamins and folates) performed in routine care * MMSE score ≥16 * Presence of an informant and caregiver, living with the patient * IAChE and/or Memantine treatment non-compulsory ; If implemented it must be effective and stable for 2 months before the selection visit and must remain stable for the duration of the study Exclusion Criteria: * Patients who refuse to adopt a low caffeine diet (eviction of tea, caffeinated sodas, chocolate in large quantities) * Current major depressive episode according to DSM-5 criteria * Another chronic pathology of the central nervous system * Major anxiety according to the clinician (consistent with the corresponding nPI-R items that must indicate a severity \>2 and an impact \>3) * Sleep disorders defined by severity and an impact on NPI-R; a patient fitted for OSA may be included if the device has been in use for 3 months and well tolerated (stable) * Decompensated heart disease or severe rhythm disorder (excluding slow, treated and stable chronic atrial fibrillation) * Active smoking * For childbearing women : pregnancy in progress or planned (A pregnancy test will be performed) * Patients who take forbidden treatment : * Psychotropic treatments introduced or modified \< 2 months before inclusion * Chronic use of CYP1A2 inducing or inhibiting drugs * All caffeine-containing specialties * Drugs that influence caffeine metabolism * Drugs that may interact with caffeine
Interventions
Caffeine
DRUG
Placebo
DRUG
Locations 17
France (17)
CHU Amiens
Amiens
NOT_YET_RECRUITING
CH Arras
Arras
NOT_YET_RECRUITING
CH Beauvais
Beauvais
NOT_YET_RECRUITING
CH Béthune
Béthune
NOT_YET_RECRUITING
CHU Caen
Caen
NOT_YET_RECRUITING
CH Calais
Calais
NOT_YET_RECRUITING
CH Dunkerque
Dunkirk
NOT_YET_RECRUITING
CH Le Quesnoy
Le Quesnoy
NOT_YET_RECRUITING
CH Lens
Lens
NOT_YET_RECRUITING
Hôpital Roger Salengro
Lille
CHU Lille consultation mémoire Les Bâteliers
Lille
NOT_YET_RECRUITING
CH Roubaix
Roubaix
NOT_YET_RECRUITING
CHU Rouen
Rouen
NOT_YET_RECRUITING
CH Saint Quentin
Saint-Quentin
NOT_YET_RECRUITING
CH Seclin
Seclin
NOT_YET_RECRUITING
CH Tourcoing
Tourcoing
NOT_YET_RECRUITING
CH Valenciennes
Valenciennes
NOT_YET_RECRUITING
Technical details
Status
Recruiting
Phase
Phase 3
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
50 Years
Healthy volunteers
No
Start date
01.03.2021
Completion date
01.12.2027
Registry ID
NCT04570085
Source
clinicaltrials.gov
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