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The Effects of Metformin on Functional Capacity in Individuals With Peripheral Artery Disease-Related Intermittent Claudication

Primary Purpose

Peripheral Arterial Disease, Intermittent Claudication

Status
Terminated
Phase
Phase 4
Locations
Australia
Study Type
Interventional
Intervention
Metformin
Placebo
Sponsored by
Baker Heart and Diabetes Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Peripheral Arterial Disease focused on measuring Peripheral Arterial Disease, Intermittent Claudication, Peripheral Vascular Diseases, Vascular Diseases, Cardiovascular Diseases, Arterial Occlusive Diseases, Atherosclerosis, Insulin Resistance, Glucose Metabolism, Blood Glucose, Metformin, Biguanides, Hypoglycemic Agents, Endothelium, Vascular, Hemorheology, Blood Circulation, Regional Blood Flow, Microcirculation, Exercise, Physical Fitness, Exercise Test, Sedentary Lifestyle, Quality of Life, Plethysmography

Eligibility Criteria

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

Inclusion Criteria:

  • Age ≥40 years old.
  • Resting ankle-brachial index (ABI) ≤0.90 in the limiting leg(s), or a >20% reduction in the ABI measured immediately post-exercise where the resting ABI is >0.90. In cases of incompressible arteries in the limiting leg(s) (i.e. ABI ≥1.40), a toe-brachial index (TBI) of ≤0.70 is required.
  • Peripheral artery stenosis/occlusion in the limiting leg(s), documented by duplex ultrasonography or other imaging tests.
  • Stable (i.e. 3-month history) intermittent claudication in at least one PAD-affected leg.
  • Maximum walking time during graded treadmill exercise testing (Gardner-Skinner protocol) ≥1 minute and ≤16 minutes.
  • Concurrent medications that may affect primary, secondary or exploratory endpoints have remained stable over the previous 3 months.
  • Have given signed informed consent to participate in the study.

Exclusion Criteria:

  • Identification of any other medical condition requiring immediate therapeutic intervention.
  • Clinically significant abnormal electrocardiogram (ECG) at rest or during exercise that represents a contraindication to study procedures or the study drug.
  • Myocardial infarction, unstable angina, percutaneous transluminal coronary angioplasty (PTCA), coronary artery bypass graft surgery (CABG), or other major surgery within the previous 6 months.
  • Exercise capacity limited by a factor other than PAD-related intermittent claudication.
  • Any condition that precludes valid completion of a treadmill exercise test.
  • Critical limb ischemia in either leg, defined as PAD-related chronic ischemic rest pain or skin lesions (ulcers, gangrene).
  • Previous peripheral revascularisation or other surgical treatment for PAD in the previous 6 months.
  • Known non-atherosclerotic cause of PAD.
  • Active cancer.
  • Uncontrolled hypertension (resting brachial blood pressure ≥160/100 mmHg).
  • Evidence of pharmacologically-treated or poorly controlled (i.e. HbA1c ≥7.5%) type 2 diabetes or other class of diabetes (e.g. type 1 diabetes).
  • Known intolerance or contraindication(s) to metformin.
  • Known contraindication(s) to "Definity" (perflutren lipid microsphere).
  • Participation or intention to participate in another clinical research study during the study period.
  • History of non-compliance to medical regimens or unwillingness to comply with the study protocol.
  • Any other condition that in the opinion of the Investigators would confound the evaluation and interpretation of the data.
  • Persons directly involved in the execution of the protocol.
  • Incapable of providing written informed consent due to cognitive, language, or other reasons.

Sites / Locations

  • Baker IDI Heart and Diabetes Institute

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Metformin

Placebo

Arm Description

Metformin at a maximum dose of 1000mg twice daily for 16-18 weeks (i.e. maximum of 2000mg per day).

Matching placebo twice daily for 16-18 weeks.

Outcomes

Primary Outcome Measures

Change in pain-free walking time
Pain-free walking time (time to onset of claudication) will be measured during a graded treadmill exercise test.
Change in maximum walking time
Maximum walking time will be measured during a graded treadmill exercise test.

Secondary Outcome Measures

Change in questionnaire-based markers of quality of life / perceived functional capacity
Change in endothelial function
Change in skeletal muscle blood flow response to insulin
Change in skeletal muscle blood flow response to acute exercise
Change in insulin sensitivity
Change in objectively measured physical activity / sedentary behaviour in the daily life setting.

Full Information

First Posted
February 22, 2013
Last Updated
February 7, 2016
Sponsor
Baker Heart and Diabetes Institute
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1. Study Identification

Unique Protocol Identification Number
NCT01799057
Brief Title
The Effects of Metformin on Functional Capacity in Individuals With Peripheral Artery Disease-Related Intermittent Claudication
Official Title
Randomised, Double-Blind, Placebo-Controlled, Parallel-Group Study of Metformin for the Assessment of Changes in Functional Capacity, Endothelial Function, and Hemodynamics in Individuals With Peripheral Artery Disease-Related Intermittent Claudication
Study Type
Interventional

2. Study Status

Record Verification Date
February 2016
Overall Recruitment Status
Terminated
Why Stopped
The trial has been terminated due to difficulties with recruitment.
Study Start Date
July 2013 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
December 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Baker Heart and Diabetes Institute

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine the effects of metformin on functional capacity (pain-free and maximum walking times) in individuals with peripheral artery disease (PAD)-related intermittent claudication.
Detailed Description
Background and Rationale: Metformin has demonstrable efficacy in slowing or reversing the progression of various insulin-resistant disease states - most notably type 2 diabetes and pre-diabetes. In seeking to establish proof-of-concept that insulin resistance is a suitable pathophysiological target in the treatment of PAD-related intermittent claudication (pain in the leg muscles during walking, which resolves on exercise cessation), this study will determine whether the known insulin-sensitizing effects of metformin translate to alleviation of the functional limitations imposed by claudication. Study Design: A total of 80 individuals with PAD-related intermittent claudication will be randomised (1:1) to either metformin or matching placebo for 16-18 weeks (double-blind, parallel group design). The maximum daily dose of metformin will be 2000mg (up-titrated from half this dose at 2 weeks if tolerated). Primary Hypothesis: Improvement in functional capacity follows metformin therapy in individuals with PAD-related intermittent claudication. Change in functional capacity will be assessed by the co-primary endpoints of pain-free and maximum walking times during a standard graded treadmill exercise test. Secondary Aims: Exercise testing for functional performance will be complemented by assessments of perceived physical functioning / quality of life in the daily life setting (using standard questionnaires). As previous studies have indicated cardiovascular effects of metformin incremental to blood glucose-lowering, this study will also investigate potential mechanisms of efficacy relating to the primary endpoints, including changes in endothelial function, blood flow responses to various stimuli (including insulin and acute exercise), insulin sensitivity, and physical activity / sedentary behaviours. Changes in relevant clinical data (including ankle-brachial index and limb hemodynamics by duplex scanning) will also be determined. Outcomes and Significance: The unmet clinical need of efficacious medical therapies for intermittent claudication is a growing problem given the increasing prevalence of PAD worldwide. If positive, this study will identify a new potential treatment that is already widely available. The study will also inform on novel mechanistic targets with relevance to existing and future therapeutic strategies.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Arterial Disease, Intermittent Claudication
Keywords
Peripheral Arterial Disease, Intermittent Claudication, Peripheral Vascular Diseases, Vascular Diseases, Cardiovascular Diseases, Arterial Occlusive Diseases, Atherosclerosis, Insulin Resistance, Glucose Metabolism, Blood Glucose, Metformin, Biguanides, Hypoglycemic Agents, Endothelium, Vascular, Hemorheology, Blood Circulation, Regional Blood Flow, Microcirculation, Exercise, Physical Fitness, Exercise Test, Sedentary Lifestyle, Quality of Life, Plethysmography

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
2 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Metformin
Arm Type
Experimental
Arm Description
Metformin at a maximum dose of 1000mg twice daily for 16-18 weeks (i.e. maximum of 2000mg per day).
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Matching placebo twice daily for 16-18 weeks.
Intervention Type
Drug
Intervention Name(s)
Metformin
Other Intervention Name(s)
Diaformin
Intervention Description
Participants randomized to metformin will be treated at a maximum dose of 2000mg per day (i.e. 1000mg twice daily for 16-18 weeks; up-titrated from 500mg twice daily for the first 2 weeks). Participants may complete the 16-18 week treatment intervention at the lower dose of 500mg twice daily if limited by side effects.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Participants randomized to placebo will take matching oral capsules according to the same dose schedule specified for the metformin intervention.
Primary Outcome Measure Information:
Title
Change in pain-free walking time
Description
Pain-free walking time (time to onset of claudication) will be measured during a graded treadmill exercise test.
Time Frame
Measured at baseline and following 16-18 weeks treatment
Title
Change in maximum walking time
Description
Maximum walking time will be measured during a graded treadmill exercise test.
Time Frame
Measured at baseline and following 16-18 weeks treatment
Secondary Outcome Measure Information:
Title
Change in questionnaire-based markers of quality of life / perceived functional capacity
Time Frame
Measured at baseline and following 16-18 weeks treatment
Title
Change in endothelial function
Time Frame
Measured at baseline and following 16-18 weeks treatment
Title
Change in skeletal muscle blood flow response to insulin
Time Frame
Measured at baseline and following 16-18 weeks treatment
Title
Change in skeletal muscle blood flow response to acute exercise
Time Frame
Measured at baseline and following 16-18 weeks treatment
Title
Change in insulin sensitivity
Time Frame
Measured at baseline and following 16-18 weeks treatment
Title
Change in objectively measured physical activity / sedentary behaviour in the daily life setting.
Time Frame
Measured at baseline and following 16-18 weeks treatment
Other Pre-specified Outcome Measures:
Title
Change in glucose uptake and insulin signalling mechanisms in skeletal muscle (exploratory endpoint)
Time Frame
Measured at baseline and following 16-18 weeks treatment
Title
Change in skeletal muscle oxidative capacity and substrate utilization (exploratory endpoint)
Time Frame
Measured at baseline and following 16-18 weeks treatment
Title
Change in inflammation, fibrinolysis and coagulation (exploratory endpoint)
Time Frame
Measured at baseline and following 16-18 weeks treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥40 years old. Resting ankle-brachial index (ABI) ≤0.90 in the limiting leg(s), or a >20% reduction in the ABI measured immediately post-exercise where the resting ABI is >0.90. In cases of incompressible arteries in the limiting leg(s) (i.e. ABI ≥1.40), a toe-brachial index (TBI) of ≤0.70 is required. Peripheral artery stenosis/occlusion in the limiting leg(s), documented by duplex ultrasonography or other imaging tests. Stable (i.e. 3-month history) intermittent claudication in at least one PAD-affected leg. Maximum walking time during graded treadmill exercise testing (Gardner-Skinner protocol) ≥1 minute and ≤16 minutes. Concurrent medications that may affect primary, secondary or exploratory endpoints have remained stable over the previous 3 months. Have given signed informed consent to participate in the study. Exclusion Criteria: Identification of any other medical condition requiring immediate therapeutic intervention. Clinically significant abnormal electrocardiogram (ECG) at rest or during exercise that represents a contraindication to study procedures or the study drug. Myocardial infarction, unstable angina, percutaneous transluminal coronary angioplasty (PTCA), coronary artery bypass graft surgery (CABG), or other major surgery within the previous 6 months. Exercise capacity limited by a factor other than PAD-related intermittent claudication. Any condition that precludes valid completion of a treadmill exercise test. Critical limb ischemia in either leg, defined as PAD-related chronic ischemic rest pain or skin lesions (ulcers, gangrene). Previous peripheral revascularisation or other surgical treatment for PAD in the previous 6 months. Known non-atherosclerotic cause of PAD. Active cancer. Uncontrolled hypertension (resting brachial blood pressure ≥160/100 mmHg). Evidence of pharmacologically-treated or poorly controlled (i.e. HbA1c ≥7.5%) type 2 diabetes or other class of diabetes (e.g. type 1 diabetes). Known intolerance or contraindication(s) to metformin. Known contraindication(s) to "Definity" (perflutren lipid microsphere). Participation or intention to participate in another clinical research study during the study period. History of non-compliance to medical regimens or unwillingness to comply with the study protocol. Any other condition that in the opinion of the Investigators would confound the evaluation and interpretation of the data. Persons directly involved in the execution of the protocol. Incapable of providing written informed consent due to cognitive, language, or other reasons.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bronwyn A Kingwell, PhD
Organizational Affiliation
Baker Heart and Diabetes Institute
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Stephen J Duffy, MD, PhD
Organizational Affiliation
Baker Heart and Diabetes Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Baker IDI Heart and Diabetes Institute
City
Melbourne
State/Province
Victoria
ZIP/Postal Code
3004
Country
Australia

12. IPD Sharing Statement

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The Effects of Metformin on Functional Capacity in Individuals With Peripheral Artery Disease-Related Intermittent Claudication

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