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Donepezil Double Blind Trial for ECT Memory Disfunction

Donepezil Double Blind Trial for ECT Memory Disfunction

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00465283
Enrollment
40
Registered
2007-04-24
Start date
2007-05-31
Completion date
2010-01-31
Last updated
2009-01-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Schizoaffective Disorder, Schizophrenia, Schizophreniform Disorder

Keywords

Donepezil, ECT, Memory Disfunction

Brief summary

This is a double blind randomized investigation of donepezil for patients suffering from schizophrenia, undergoing ECT. Patients will be randomized to receive either donezepil or plasebo, in order to gauge whether donezepil has a protective effect on memory disfunction, while patients are treated with ECT. Several parameters will be invistigated at baseline: general psychopathological measures, memory function scales, side effects scales. The same measurements will be taken throughout the trial and one month after ending the ECT.

Interventions

DRUGDonepezil

Tab.Donepezil 5 mg once daily during ECT treatment and the month after the last ECT treatment

Sponsors

BeerYaakov Mental Health Center
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Schizophrenia, Schizoaffective disorder, schizophreniform disorder patients who meet criteria for diagnoses by DSM-IV criteria and evaluated by the Structured Clinical Interview for DSM-IV (SCID)

Exclusion criteria

* History of serious neurological disorders including neurodegenerative deseases, mental retardation, substance and/or alcohol dependence. * Pregnant women * Patients who recieved ECT within 6 month * Patients whith contraindication to Donepezil treatment. * Patients with Lithium treatment

Design outcomes

Primary

MeasureTime frame
Data will be analyzed using SPSS for Windows.after 5 ECT treatments
Results of the memory and neurocognitive measures will be examinedafter 8 ECT treatments
using repeated MANOVA with before, within and after ECT treatment.1 month after the last ECT treatment

Countries

Israel

Contacts

Primary ContactTali Nachshoni, MD
bynachshoni@beer-ness.health.gov.il972-8-9258372
Backup ContactMarina Kupchik, MD
kupchik@beer-ness.health.gov.il972-89258382

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026