Combination Treatment Study for Memory Impairment and Depression

PHASE4CompletedINTERVENTIONAL
Enrollment

86

Participants

Timeline

Start Date

September 30, 2011

Primary Completion Date

January 31, 2016

Study Completion Date

January 31, 2016

Conditions
DepressionMild Cognitive Impairment
Interventions
DRUG

Donepezil

Donepezil 5mg will be given for 6 weeks and if tolerated, the dose will be increased to 10 mg per day. The dose range of 5 to 10 mg per day is the recommended dose for donepezil in the treatment of mild to moderate Alzheimer's disease.

DRUG

Placebo

A placebo capsule will be given to randomized subjects for the starting at week 16 and continuing for the remainder of the study. This group will not receive donepezil as treatment.

DRUG

Citalopram

Citalopram tablet will be given to subjects during an 8 week flexible dosing open treatment. If subjects respond to citalopram treatment they will be randomized to add-on donepezil/placebo.

DRUG

Venlafaxine

Venlafaxine tablet will be given to subjects during an 8 week flexible dosing open treatment if they did not respond to citalopram. If subjects respond to venlafaxine treatment they will be randomized to add-on donepezil/placebo.

Trial Locations (2)

10032

New York State Psychiatric Institute, New York

27710

Duke University, Durham

All Listed Sponsors
collaborator

National Institute on Aging (NIA)

NIH

lead

New York State Psychiatric Institute

OTHER

NCT01658228 - Combination Treatment Study for Memory Impairment and Depression | Biotech Hunter | Biotech Hunter