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Acetylcholinesterase Inhibitors to Improve Cognitive Function and Overall Rehabilitation After a Stroke

Primary Purpose

Cerebrovascular Accident

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Galantamine
Donepezil
Sponsored by
University of Pittsburgh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cerebrovascular Accident focused on measuring Cholinesterase Inhibitors, Elderly, Stroke, Cognition

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Admitted to a rehabilitation hospital with primary diagnosis of ischemic stroke (cardiovascular accident) Stroke was within 30 days of being admitted Medically stable Presence of memory and/or attentional impairments and evidence that these impairments were not present or were less severe prior to the stroke (assessed via interview with family) Approval by individual's attending physician at the rehabilitation hospital Exclusion Criteria: Aphasia or cognitive (or behavioral) impairments severe enough to prevent valid neuropsychiatric assessment Currently experiencing a major depressive episode (unless treated and in partial remission, assessed using the Primary Care Evaluation of Mental Disorders) Current psychosis or mania History of substance or alcohol abuse or dependence within three months of study entry Currently taking a cholinomimetic drug Medical condition with known sensitivity to donepezil (e.g., slower than normal heart rate, supraventricular cardiac conduction defects, severe asthma or obstructive pulmonary disease, active upper gastrointestinal bleed, or gastric/duodenal ulcer if not on acid-blocking agent) Informed that taking donepezil is medically inadvisable Current use of any anticholinergic medication (e.g., for bladder spasm)

Sites / Locations

  • University of Pittsburgh Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Galantamine

Donepezil

Arm Description

Galantamine for 12 weeks

Donepezil for 12 weeks

Outcomes

Primary Outcome Measures

Physical Function (Measured by the FIM-motor)
Score on Functional Independence Measure (FIM) motor score, where 7 indicates total assistance/complete dependence and 91 is complete independence

Secondary Outcome Measures

Medication Tolerability
Number of participants who withdrew due to side effects.

Full Information

First Posted
September 26, 2005
Last Updated
November 9, 2017
Sponsor
University of Pittsburgh
Collaborators
National Institute of Mental Health (NIMH)
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1. Study Identification

Unique Protocol Identification Number
NCT00227994
Brief Title
Acetylcholinesterase Inhibitors to Improve Cognitive Function and Overall Rehabilitation After a Stroke
Official Title
Donepezil/ Galantamine in the Treatment of Post-stroke Cognitively Impaired Rehabilitating Elderly
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
April 2003 (undefined)
Primary Completion Date
January 2005 (Actual)
Study Completion Date
March 2005 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Pittsburgh
Collaborators
National Institute of Mental Health (NIMH)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study will evaluate the effectiveness of treatment with acetylcholinesterase inhibitors in improving cognitive function and overall rehabilitation in elderly stroke survivors.
Detailed Description
Cognitive impairment is a common result of a stroke and can be detrimental to recovery. It can negatively affect both mental and physical functioning, thereby complicating the rehabilitation process. Although much research has targeted the effects of long-term cognitive impairment after a stroke, very little research has been done to examine the incidence and course of cognitive impairment during the first three months following a stroke. These first three months are the most important in terms of regaining function. Acetylcholinesterase inhibitors have been beneficial to both sufferers of vascular dementia and Alzheimer's disease. They may also be a useful pharmacologic intervention to enhance post-stroke rehabilitation. This study will compare the effectiveness of two acetylcholinesterase inhibitors, galantamine and donepezil, in improving cognitive function and overall rehabilitation in elderly stroke survivors. Participants in this open label study will be randomly assigned to receive either galantamine or donepezil for 12 weeks. Participants assigned to receive galantamine will receive 4 mg twice a day for 4 weeks, 8 mg twice a day for the next 4 weeks, and 12 mg twice a day for the remainder of the study. Participants assigned to receive donepezil will receive 5 mg twice a day for 6 weeks, and then 10 mg twice a day for the next 6 weeks. Functional independence will be measured at baseline and Weeks 2 and 12. In addition, a pre-stroke level of functional independence will be obtained through a structured interview with participants and their families. Participants will also be monitored for signs of depression and medication side effects throughout the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cerebrovascular Accident
Keywords
Cholinesterase Inhibitors, Elderly, Stroke, Cognition

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Galantamine
Arm Type
Experimental
Arm Description
Galantamine for 12 weeks
Arm Title
Donepezil
Arm Type
Experimental
Arm Description
Donepezil for 12 weeks
Intervention Type
Drug
Intervention Name(s)
Galantamine
Other Intervention Name(s)
Razadyne
Intervention Description
Participants assigned to receive galantamine will receive 4 mg twice a day for 4 weeks, 8 mg twice a day for the next 4 weeks, and 12 mg twice a day for the remainder of the study.
Intervention Type
Drug
Intervention Name(s)
Donepezil
Other Intervention Name(s)
Aricept
Intervention Description
Participants assigned to receive donepezil will receive 5 mg twice a day for 6 weeks, and then 10 mg twice a day for the next 6 weeks.
Primary Outcome Measure Information:
Title
Physical Function (Measured by the FIM-motor)
Description
Score on Functional Independence Measure (FIM) motor score, where 7 indicates total assistance/complete dependence and 91 is complete independence
Time Frame
Measured at weeks 0 and 12
Secondary Outcome Measure Information:
Title
Medication Tolerability
Description
Number of participants who withdrew due to side effects.
Time Frame
Measured throughout the study

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Admitted to a rehabilitation hospital with primary diagnosis of ischemic stroke (cardiovascular accident) Stroke was within 30 days of being admitted Medically stable Presence of memory and/or attentional impairments and evidence that these impairments were not present or were less severe prior to the stroke (assessed via interview with family) Approval by individual's attending physician at the rehabilitation hospital Exclusion Criteria: Aphasia or cognitive (or behavioral) impairments severe enough to prevent valid neuropsychiatric assessment Currently experiencing a major depressive episode (unless treated and in partial remission, assessed using the Primary Care Evaluation of Mental Disorders) Current psychosis or mania History of substance or alcohol abuse or dependence within three months of study entry Currently taking a cholinomimetic drug Medical condition with known sensitivity to donepezil (e.g., slower than normal heart rate, supraventricular cardiac conduction defects, severe asthma or obstructive pulmonary disease, active upper gastrointestinal bleed, or gastric/duodenal ulcer if not on acid-blocking agent) Informed that taking donepezil is medically inadvisable Current use of any anticholinergic medication (e.g., for bladder spasm)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eric J. Lenze, MD
Organizational Affiliation
University of Pittsburgh Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Pittsburgh Medical Center
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15260
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
study has small sample size and is unlikely to be useful for data sharing efforts; however, interested researchers can contact the first author via email.
Citations:
PubMed Identifier
18667813
Citation
Whyte EM, Lenze EJ, Butters M, Skidmore E, Koenig K, Dew MA, Penrod L, Mulsant BH, Pollock BG, Cabacungan L, Reynolds CF 3rd, Munin MC. An open-label pilot study of acetylcholinesterase inhibitors to promote functional recovery in elderly cognitively impaired stroke patients. Cerebrovasc Dis. 2008;26(3):317-21. doi: 10.1159/000149580. Epub 2008 Jul 31.
Results Reference
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Acetylcholinesterase Inhibitors to Improve Cognitive Function and Overall Rehabilitation After a Stroke

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