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The Clinical Study of Pitavastatin Treatment for Group of Mild to Moderate Alzheimer's Disease (PIT-ROAD)

Primary Purpose

Alzheimer Disease, Hypercholesterolemia

Status
Terminated
Phase
Not Applicable
Locations
Japan
Study Type
Interventional
Intervention
Pitavastatin
cholesterol-lowering medicine other than statin(e.g.,Ezetimibe,Colestimide)
Sponsored by
Osaka University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alzheimer Disease focused on measuring Pitavastatin, Statins, Donepezil, Alzheimer's Disease, Hypercholesterolemia, ADAS-Jcog, Alzheimer Disease (MMSE 15-23 and CDR1 or 2)

Eligibility Criteria

20 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Alzheimer's Disease patients (15 ≤ MMSE total score ≤ 23, CDR "1" or "2")
  • Patients with hypercholesterolemia
  • Patients who have taken donepezil more than 3 months stably
  • Both patients and care-givers must be more than 20 years old

Exclusion Criteria:

  • Women with pregnancy or breast-feeding
  • Malignant tumor
  • Cerebrovascular disorder or myocardial infarction prior to 12 weeks
  • Heart failure [New York Heart Association (NYHA) class III or IV]
  • Hepatic or renal dysfunction
  • Severe hypertension
  • Hypothyroidism, hereditary muscular disease, history of drug-induced myopathy
  • Current involvement in another investigational drug study
  • Alcoholism, drug abuse

Sites / Locations

  • Osaka University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

Outcomes

Primary Outcome Measures

Alzheimer's Disease Assessment Scale-cognitive Component-Japanese Version(ADAS-Jcog)
Alzheimer's Disease Assessment Scale-cognitive component-Japanese version is a cognitive test for Alzheimer's disease. This test includes some aspects that assess memory ,orientation, language, praxis, and so on. The possible range of this test is 0-70 points.Higher total points indicate more impairment.

Secondary Outcome Measures

MMSE, Neuropsychiatric Inventory, GDS-15, Zarit Burden Scale, Physical Self-Maintenance Scale, IADL, Everyday Memory Checklist, TC, HDL-C, Non HDL-C*, Apo A1, Apo B, Apo E *: Non HDL-C = (TC) - (HDL-C)
Mini-Mental State Examination(MMSE),Geriatric Depression Scale-15(GDS-15),Instrumental Activities of Daily Living Scale(IADL),Total Cholesterol(TC)

Full Information

First Posted
October 22, 2007
Last Updated
May 14, 2012
Sponsor
Osaka University
Collaborators
Kowa Company, Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT00548145
Brief Title
The Clinical Study of Pitavastatin Treatment for Group of Mild to Moderate Alzheimer's Disease
Acronym
PIT-ROAD
Study Type
Interventional

2. Study Status

Record Verification Date
May 2012
Overall Recruitment Status
Terminated
Study Start Date
November 2007 (undefined)
Primary Completion Date
October 2011 (Actual)
Study Completion Date
March 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Osaka University
Collaborators
Kowa Company, Ltd.

4. Oversight

5. Study Description

Brief Summary
Some studies suggest that statin medications may be effective against Alzheimer's disease. However, this has not been proven. The purpose of this study is to evaluate the efficacy of pitavastatin in patients with mild to moderate Alzheimer's disease and hypercholesterolemia.
Detailed Description
The PIT-ROAD study will include 50 patients who have taken donepezil more than 3 months stably. This study will see how the use of a particular statin medication, pitavastatin, affects ADAS-Jcog score etc. and cholesterol. Participants will be given a full information of the study and written informed consent should be obtained before entering the study. Participants will take part in 5 visits over the course of 12 months. If participants have taken cholesterol lowering drug, they will have wash-out period at least 4weeks. Participants will undergo 8 tests (ADAS-Jcog etc., baseline and month 12 visits), complete a medical history questionnaire (baseline), complete medication side effect review through questionnaire and/or blood sample (all visits). Participants will be randomly assigned to receive either pitavastatin or other cholesterol lowering medication for 12 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer Disease, Hypercholesterolemia
Keywords
Pitavastatin, Statins, Donepezil, Alzheimer's Disease, Hypercholesterolemia, ADAS-Jcog, Alzheimer Disease (MMSE 15-23 and CDR1 or 2)

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
38 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Title
2
Arm Type
Active Comparator
Intervention Type
Drug
Intervention Name(s)
Pitavastatin
Intervention Description
2 mg by orally/day Duration: 12 months
Intervention Type
Drug
Intervention Name(s)
cholesterol-lowering medicine other than statin(e.g.,Ezetimibe,Colestimide)
Intervention Description
duration: 12 months
Primary Outcome Measure Information:
Title
Alzheimer's Disease Assessment Scale-cognitive Component-Japanese Version(ADAS-Jcog)
Description
Alzheimer's Disease Assessment Scale-cognitive component-Japanese version is a cognitive test for Alzheimer's disease. This test includes some aspects that assess memory ,orientation, language, praxis, and so on. The possible range of this test is 0-70 points.Higher total points indicate more impairment.
Time Frame
baseline and 12 months
Secondary Outcome Measure Information:
Title
MMSE, Neuropsychiatric Inventory, GDS-15, Zarit Burden Scale, Physical Self-Maintenance Scale, IADL, Everyday Memory Checklist, TC, HDL-C, Non HDL-C*, Apo A1, Apo B, Apo E *: Non HDL-C = (TC) - (HDL-C)
Description
Mini-Mental State Examination(MMSE),Geriatric Depression Scale-15(GDS-15),Instrumental Activities of Daily Living Scale(IADL),Total Cholesterol(TC)
Time Frame
baseline and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Alzheimer's Disease patients (15 ≤ MMSE total score ≤ 23, CDR "1" or "2") Patients with hypercholesterolemia Patients who have taken donepezil more than 3 months stably Both patients and care-givers must be more than 20 years old Exclusion Criteria: Women with pregnancy or breast-feeding Malignant tumor Cerebrovascular disorder or myocardial infarction prior to 12 weeks Heart failure [New York Heart Association (NYHA) class III or IV] Hepatic or renal dysfunction Severe hypertension Hypothyroidism, hereditary muscular disease, history of drug-induced myopathy Current involvement in another investigational drug study Alcoholism, drug abuse
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hiroaki Kazui, Ph.D.
Organizational Affiliation
Osaka University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Osaka University Hospital
City
Suita
State/Province
Osaka
ZIP/Postal Code
565-0871
Country
Japan

12. IPD Sharing Statement

Links:
URL
http://www.med.osaka-u.ac.jp/pub/psy/www/en/index.html
Description
Related Info

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The Clinical Study of Pitavastatin Treatment for Group of Mild to Moderate Alzheimer's Disease

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