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Telmisartan vs. Perindopril in Mild-Moderate Alzheimer's Disease Patients (SARTAN-AD)

Primary Purpose

Alzheimer's Disease

Status
Recruiting
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Perindopril
Telmisartan
Sponsored by
Sunnybrook Health Sciences Centre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alzheimer's Disease focused on measuring Alzheimer's Disease, Perindopril, Telmisartan, Brain atrophy

Eligibility Criteria

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

Inclusion criteria

  1. Diagnosis of Probable AD dementia or Possible AD dementia due to concomitant cerebrovascular disease (as permitted by the study exclusion criteria), using the 2011 McKhann criteria.
  2. Previous brain MRI or CT scan to rule out exclusionary pathology, and absence of stepwise decline since the previous scan.
  3. Age 50 years or older
  4. Standardized Mini Mental State Examination (SMMSE) score of 16-27 at screening visit
  5. Sufficient hearing and vision to participate in testing as per investigator's judgement
  6. Sufficient fluency in English to understand instructions and to be able to complete SMMSE
  7. A study partner who in the opinion of the study investigator has regular interaction with the participant, can be present for study visits, can provide a collateral history and can ensure compliance with study procedures
  8. HbA1C <8.5%. Patients with stable type II diabetes are eligible for the study if there have been no severe hypoglycemic events requiring third party intervention (e.g. emergency department visit) for 6 months prior to randomization
  9. Patients on cholinesterase inhibitors or memantine, medications for vascular risk factors (e.g., hypertension, cholesterol, diabetes), or on psychotropic medications must be on a stable dose for 30 days prior to randomization.

Exclusion criteria

  1. Intolerance, or any contraindications, to study medications
  2. Average SBP <110mmHg or average DBP <60 mmHg during screening
  3. Familial autosomal dominant form of Alzheimer's disease
  4. Creatinine clearance less than or equal to 30ml/min
  5. Serum potassium > 5.5 mEq/L
  6. ALT 3x > the upper limit of normal (ULN)
  7. History of angioedema
  8. Co-morbid acute or chronic conditions (including type I diabetes mellitus, other neurological conditions such as Parkinson's disease, psychiatric disorders, and severe or unstable medical conditions) that could confound assessments or would, in the judgment of the investigator, make the subject inappropriate for entry into this study
  9. Any of the following findings on previous CT/MRI or on screening MRI:

    Exclusionary Finding: Malignant tumour Brain Location: Anywhere Size: Any Exclusionary Number: Any

    Exclusionary Finding: Tumour with significant mass effect Brain Location: Anywhere Size: Sufficient for mass effect Exclusionary Number: Any

    Exclusionary Finding: Vascular malformations Brain Location: Anywhere Size: Any Exclusionary Number: Any

    Exclusionary Finding: Subdural hematoma Brain Location: Anywhere Size: Any Exclusionary Number: Any

    Exclusionary Finding: Intracerebral hemorrhage Brain Location: Anywhere Size: Any Exclusionary Number: Any

    Exclusionary Finding: Cerebral microbleeds, Brain Location: Anywhere Size: Any Exclusionary Number: more than 5

    Exclusionary Finding: Superficial siderosis (SS) Brain Location: Cortex Size: Any Exclusionary Number: >1 instance of focal SS

    Exclusionary Finding: Ischemic infarct Brain Location: Cortex Size: >1.5 cm in diameter Exclusionary Number: Any

    Exclusionary Finding: Ischemic infarct Brain Location: Cortex Size: ≤1.5 cm in diameter Exclusionary Number: more than 1

    Exclusionary Finding: Fazekas score 3 with white matter hyperintensity band along the lateral surface of the ventricles >0.5 cm in width

    Exclusionary Finding: Ischemic infarct Brain Location: White matter Size: >1.5 cm in diameter Exclusionary Number: Any

    Exclusionary Finding: Ischemic infarct Brain Location: White matter Size: 1.0-1.5 cm in diameter Exclusionary Number: More than 2

    Exclusionary Finding: Ischemic infarct Brain Location: Basal ganglia Size: >1.0 cm in diameter Exclusionary Number: Any

    Exclusionary Finding: Ischemic infarct Brain Location: Basal ganglia and white matter Size: ≤1.0 cm in diameter Exclusionary Number: More than 4

    Exclusionary Finding: Strategic infarct Brain Location: Thalamus Size: Any Exclusionary Number: Any

    Exclusionary Finding: Strategic infarct Brain Location: Hippocampus, Size: Any Exclusionary Number: Any

  10. Inability to perform the study procedures, including claustrophobia or contraindications for MRI
  11. Currently on or has taken an angiotensin receptor blocker within 12 months of randomization visit
  12. Resides in a nursing home (participants who reside in retirement homes may be included if they have a study partner who meets inclusion criterion #8)
  13. Current major depression by clinical history or score greater than 18 on the Cornell Scale for Depression in Dementia
  14. Documented potential cardiac source of brain infarction such as mechanical valve or atrial fibrillation that is untreated or treated with warfarin or an antiplatelet agent; atrial fibrillation treated with a novel oral anticoagulant is permitted, as is a history of remote, transient atrial fibrillation that has not recurred

Sites / Locations

  • University of CalgaryRecruiting
  • University of LethbridgeRecruiting
  • UBC HospitalRecruiting
  • Hamilton General HospitalRecruiting
  • Parkwood Institute
  • Centre for Memory and Aging
  • Sunnybrook Health Sciences CentreRecruiting
  • St. Michael's HospitalRecruiting
  • Baycrest Health SciencesRecruiting
  • Centre for Addiction and Mental Health (CAMH)Recruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Telmisartan

Perindopril

Arm Description

Telmisartan 40 mg or 80 mg/day (depending on age and tolerability)

Perindopril 2 mg, 4 mg or 8 mg/day (depending on kidney function and tolerability)

Outcomes

Primary Outcome Measures

Ventricular enlargement
Change in ventricular size, on 3D T1 MR imaging, after 12 months of treatment
Safety - Blood pressure
Change in blood pressure (BP) measurements after 12 months of treatment.
Safety - Vital signs
Change in vital sign (heart rate, pulse) measurements after 12 months of treatment.
Safety - Electrolytes
Change in electrolyte measurements (Na, K) after 12 months of treatment.
Safety - Adverse Events
Adverse events and serious adverse events over 12 months of treatment.

Secondary Outcome Measures

Hippocampal volume
Change in hippocampal volume measurements after 12 months of treatment
Grey/White matter volume
Volume of grey and white matter in the cingulate, parietotemporal and dorsolateral frontal regions after 12 months of treatment
Cognitive and functional measures
Determine comparative efficacy of perindopril vs. telmisartan on cognitive and functional measures and on other structural brain imaging measures in this participant population

Full Information

First Posted
November 29, 2013
Last Updated
May 3, 2022
Sponsor
Sunnybrook Health Sciences Centre
Collaborators
Alzheimer's Drug Discovery Foundation, Weston Brain Institute
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1. Study Identification

Unique Protocol Identification Number
NCT02085265
Brief Title
Telmisartan vs. Perindopril in Mild-Moderate Alzheimer's Disease Patients
Acronym
SARTAN-AD
Official Title
The SARTAN-AD Trial: A Randomized, Open Label, Proof of Concept Study of Telmisartan vs. Perindopril in Mild-Moderate Alzheimer's Disease Patients
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 2014 (undefined)
Primary Completion Date
September 2023 (Anticipated)
Study Completion Date
September 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sunnybrook Health Sciences Centre
Collaborators
Alzheimer's Drug Discovery Foundation, Weston Brain Institute

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
To conduct a proof of concept study in patients with mild to moderate Alzheimer's Disease in order to determine if there is less global brain atrophy over one year, as measured by ventricular enlargement as a primary outcome measure, when patients are randomized to treatment with an angiotensin receptor blocker (ARB) compared to an angiotensin converting enzyme inhibitor (ACEI).
Detailed Description
This study uses a simple validated measure of brain atrophy as a surrogate marker in a repurposing effort that could recast an antihypertensive medication as a cognitive enhancer/neuroprotective agent and possibly as a drug of choice for Alzheimer patients and patients at risk for AD. If the proof of concept result is positive, a larger study would be warranted with potential practice-changing impact.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer's Disease
Keywords
Alzheimer's Disease, Perindopril, Telmisartan, Brain atrophy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Telmisartan
Arm Type
Experimental
Arm Description
Telmisartan 40 mg or 80 mg/day (depending on age and tolerability)
Arm Title
Perindopril
Arm Type
Active Comparator
Arm Description
Perindopril 2 mg, 4 mg or 8 mg/day (depending on kidney function and tolerability)
Intervention Type
Drug
Intervention Name(s)
Perindopril
Other Intervention Name(s)
Coversyl
Intervention Description
Perindopril 2 mg, 4 mg or 8 mg/day (depending on kidney function and tolerability)
Intervention Type
Drug
Intervention Name(s)
Telmisartan
Other Intervention Name(s)
Micardis
Intervention Description
Telmisartan 40 mg or 80 mg/day (depending on age and tolerability)
Primary Outcome Measure Information:
Title
Ventricular enlargement
Description
Change in ventricular size, on 3D T1 MR imaging, after 12 months of treatment
Time Frame
12 months
Title
Safety - Blood pressure
Description
Change in blood pressure (BP) measurements after 12 months of treatment.
Time Frame
12 months
Title
Safety - Vital signs
Description
Change in vital sign (heart rate, pulse) measurements after 12 months of treatment.
Time Frame
12 months
Title
Safety - Electrolytes
Description
Change in electrolyte measurements (Na, K) after 12 months of treatment.
Time Frame
12 months
Title
Safety - Adverse Events
Description
Adverse events and serious adverse events over 12 months of treatment.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Hippocampal volume
Description
Change in hippocampal volume measurements after 12 months of treatment
Time Frame
12 months
Title
Grey/White matter volume
Description
Volume of grey and white matter in the cingulate, parietotemporal and dorsolateral frontal regions after 12 months of treatment
Time Frame
12 months
Title
Cognitive and functional measures
Description
Determine comparative efficacy of perindopril vs. telmisartan on cognitive and functional measures and on other structural brain imaging measures in this participant population
Time Frame
6 and 12 months
Other Pre-specified Outcome Measures:
Title
Neuropsychiatric Measures
Description
Assess the comparative treatment responsiveness of neuropsychiatric measures and obtain pilot data
Time Frame
6 & 12 months
Title
Treatment responsiveness of Diffusion Tensor Imaging (DTI)
Description
Assess the comparative treatment responsiveness of Diffusion Tensor Imaging (DTI) and obtain pilot data
Time Frame
12 months
Title
Treatment responsiveness of resting state functional MRI (rsfMRI)
Description
Assess the comparative treatment responsiveness of multi-modal MRI, resting-state functional MRI (rsfMRI) and arterial spin labeling (in a subset of participants) and obtain pilot data.
Time Frame
12 months
Title
Quality of Life - Caregiver burden
Description
Assess the comparative response of caregiver burden after treatment using Zarit burden interview.
Time Frame
12 months
Title
Quality of Life - Health-related
Description
Assess health related quality of life after treatment using EQ-5D-5L questionnaire.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria Diagnosis of Probable AD dementia or Possible AD dementia due to concomitant cerebrovascular disease (as permitted by the study exclusion criteria), using the 2011 McKhann criteria. Previous brain MRI or CT scan to rule out exclusionary pathology, and absence of stepwise decline since the previous scan. Age 50 years or older Standardized Mini Mental State Examination (SMMSE) score of 16-27 at screening visit Sufficient hearing and vision to participate in testing as per investigator's judgement Sufficient fluency in English to understand instructions and to be able to complete SMMSE A study partner who in the opinion of the study investigator has regular interaction with the participant, can be present for study visits, can provide a collateral history and can ensure compliance with study procedures HbA1C <8.5%. Patients with stable type II diabetes are eligible for the study if there have been no severe hypoglycemic events requiring third party intervention (e.g. emergency department visit) for 6 months prior to randomization Patients on cholinesterase inhibitors or memantine, medications for vascular risk factors (e.g., hypertension, cholesterol, diabetes), or on psychotropic medications must be on a stable dose for 30 days prior to randomization. Exclusion criteria Intolerance, or any contraindications, to study medications Average SBP <110mmHg or average DBP <60 mmHg during screening Familial autosomal dominant form of Alzheimer's disease Creatinine clearance less than or equal to 30ml/min Serum potassium > 5.5 mEq/L ALT 3x > the upper limit of normal (ULN) History of angioedema Co-morbid acute or chronic conditions (including type I diabetes mellitus, other neurological conditions such as Parkinson's disease, psychiatric disorders, and severe or unstable medical conditions) that could confound assessments or would, in the judgment of the investigator, make the subject inappropriate for entry into this study Any of the following findings on previous CT/MRI or on screening MRI: Exclusionary Finding: Malignant tumour Brain Location: Anywhere Size: Any Exclusionary Number: Any Exclusionary Finding: Tumour with significant mass effect Brain Location: Anywhere Size: Sufficient for mass effect Exclusionary Number: Any Exclusionary Finding: Vascular malformations Brain Location: Anywhere Size: Any Exclusionary Number: Any Exclusionary Finding: Subdural hematoma Brain Location: Anywhere Size: Any Exclusionary Number: Any Exclusionary Finding: Intracerebral hemorrhage Brain Location: Anywhere Size: Any Exclusionary Number: Any Exclusionary Finding: Cerebral microbleeds, Brain Location: Anywhere Size: Any Exclusionary Number: more than 5 Exclusionary Finding: Superficial siderosis (SS) Brain Location: Cortex Size: Any Exclusionary Number: >1 instance of focal SS Exclusionary Finding: Ischemic infarct Brain Location: Cortex Size: >1.5 cm in diameter Exclusionary Number: Any Exclusionary Finding: Ischemic infarct Brain Location: Cortex Size: ≤1.5 cm in diameter Exclusionary Number: more than 1 Exclusionary Finding: Fazekas score 3 with white matter hyperintensity band along the lateral surface of the ventricles >0.5 cm in width Exclusionary Finding: Ischemic infarct Brain Location: White matter Size: >1.5 cm in diameter Exclusionary Number: Any Exclusionary Finding: Ischemic infarct Brain Location: White matter Size: 1.0-1.5 cm in diameter Exclusionary Number: More than 2 Exclusionary Finding: Ischemic infarct Brain Location: Basal ganglia Size: >1.0 cm in diameter Exclusionary Number: Any Exclusionary Finding: Ischemic infarct Brain Location: Basal ganglia and white matter Size: ≤1.0 cm in diameter Exclusionary Number: More than 4 Exclusionary Finding: Strategic infarct Brain Location: Thalamus Size: Any Exclusionary Number: Any Exclusionary Finding: Strategic infarct Brain Location: Hippocampus, Size: Any Exclusionary Number: Any Inability to perform the study procedures, including claustrophobia or contraindications for MRI Currently on or has taken an angiotensin receptor blocker within 12 months of randomization visit Resides in a nursing home (participants who reside in retirement homes may be included if they have a study partner who meets inclusion criterion #8) Current major depression by clinical history or score greater than 18 on the Cornell Scale for Depression in Dementia Documented potential cardiac source of brain infarction such as mechanical valve or atrial fibrillation that is untreated or treated with warfarin or an antiplatelet agent; atrial fibrillation treated with a novel oral anticoagulant is permitted, as is a history of remote, transient atrial fibrillation that has not recurred
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sandra Black, MD
Phone
416.480.4551
Email
sandra.black@sunnybrook.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Ljubica Zotovic, MD
Phone
416.480.6100
Ext
3004
Email
ljubica.zotovic@sunnybrook.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sandra Black, MD
Organizational Affiliation
Sunnybrook Health Sciences Centre
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Krista Lanctot, PhD
Organizational Affiliation
Sunnybrook Research Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Calgary
City
Calgary
State/Province
Alberta
ZIP/Postal Code
T2N 4N1
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Karyn Fischer, RN
Phone
403-220-8394
Email
Karyn.Fischer@albertahealthservices.ca
First Name & Middle Initial & Last Name & Degree
Eric Smith, MD
Facility Name
University of Lethbridge
City
Lethbridge
State/Province
Alberta
ZIP/Postal Code
T1K 6T5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
John Kennedy, MD
First Name & Middle Initial & Last Name & Degree
Robert Sutherland, PhD
Facility Name
UBC Hospital
City
Vancouver
State/Province
British Columbia
ZIP/Postal Code
V6T 2B5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michele Assaly, M.A.
Phone
604-822-1782
Email
Michele.Assaly@vch.ca
First Name & Middle Initial & Last Name & Degree
Robin Hsiung, MD
Facility Name
Hamilton General Hospital
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8L 2X2
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Shuhira Himed
Phone
905.521.2100
Ext
44468
Email
himed@hhsc.ca
First Name & Middle Initial & Last Name & Degree
Demetrios (James) Sahlas, MD
Facility Name
Parkwood Institute
City
London
State/Province
Ontario
ZIP/Postal Code
N6C 4R3
Country
Canada
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rebecca Shostak
Phone
519-685-4292
Ext
45609
Email
rebecca.shostak@sjhc.london.on.ca
First Name & Middle Initial & Last Name & Degree
Michael Borrie, MD
Facility Name
Centre for Memory and Aging
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4G 3E8
Country
Canada
Individual Site Status
Completed
Facility Name
Sunnybrook Health Sciences Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4N 3M5
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anna Malakhova
Phone
416-480-6100
Ext
63867
Email
anna.malakhova@sunnybrook.ca
First Name & Middle Initial & Last Name & Degree
Ljubica Zotovic
Phone
416-480-6100
Ext
3004
Email
ljubica.zotovic@sunnybrook.ca
First Name & Middle Initial & Last Name & Degree
Sandra Black, MD
Facility Name
St. Michael's Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5B 1W8
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Corinne Fischer, MD
Facility Name
Baycrest Health Sciences
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M6A 2E1
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Naga Avvaru
Phone
(416) 785-2500
Ext
3627
Email
navvaru@research.baycrest.org
First Name & Middle Initial & Last Name & Degree
Howard Chertkow, MD
Facility Name
Centre for Addiction and Mental Health (CAMH)
City
Toronto
State/Province
Ontario
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dewi Clark
Phone
416-535-8501
Ext
30409
Email
Dewi.Clark@camh.ca
First Name & Middle Initial & Last Name & Degree
Sanjeev Kumar, MD

12. IPD Sharing Statement

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Telmisartan vs. Perindopril in Mild-Moderate Alzheimer's Disease Patients

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