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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/ct2/show/NCT01799057




Registration number
NCT01799057
Ethics application status
Date submitted
22/02/2013
Date registered
26/02/2013
Date last updated
9/02/2016

Titles & IDs
Public title
The Effects of Metformin on Functional Capacity in Individuals With Peripheral Artery Disease-Related Intermittent Claudication
Scientific 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
Secondary ID [1] 0 0
493/12
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Peripheral Arterial Disease 0 0
Intermittent Claudication 0 0
Condition category
Condition code
Cardiovascular 0 0 0 0
Diseases of the vasculature and circulation including the lymphatic system

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - Metformin
Treatment: Drugs - Placebo

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

Placebo Comparator: Placebo - Matching placebo twice daily for 16-18 weeks.


Treatment: Drugs: Metformin
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.

Treatment: Drugs: Placebo
Participants randomized to placebo will take matching oral capsules according to the same dose schedule specified for the metformin intervention.
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
Change in pain-free walking time
Timepoint [1] 0 0
Measured at baseline and following 16-18 weeks treatment
Primary outcome [2] 0 0
Change in maximum walking time
Timepoint [2] 0 0
Measured at baseline and following 16-18 weeks treatment
Secondary outcome [1] 0 0
Change in questionnaire-based markers of quality of life / perceived functional capacity
Timepoint [1] 0 0
Measured at baseline and following 16-18 weeks treatment
Secondary outcome [2] 0 0
Change in endothelial function
Timepoint [2] 0 0
Measured at baseline and following 16-18 weeks treatment
Secondary outcome [3] 0 0
Change in skeletal muscle blood flow response to insulin
Timepoint [3] 0 0
Measured at baseline and following 16-18 weeks treatment
Secondary outcome [4] 0 0
Change in skeletal muscle blood flow response to acute exercise
Timepoint [4] 0 0
Measured at baseline and following 16-18 weeks treatment
Secondary outcome [5] 0 0
Change in insulin sensitivity
Timepoint [5] 0 0
Measured at baseline and following 16-18 weeks treatment
Secondary outcome [6] 0 0
Change in objectively measured physical activity / sedentary behaviour in the daily life setting.
Timepoint [6] 0 0
Measured at baseline and following 16-18 weeks treatment

Eligibility
Key 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.
Minimum age
40 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key 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.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 4
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Terminated
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
1/07/2013
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
1/12/2014
Sample size
Target
Accrual to date
Final
2
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 0 0
Baker IDI Heart and Diabetes Institute - Melbourne
Recruitment postcode(s) [1] 0 0
3004 - Melbourne

Funding & Sponsors
Primary sponsor type
Other
Name
Baker Heart and Diabetes Institute
Address
Country

Ethics approval
Ethics application status

Summary
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.
Trial website
https://clinicaltrials.gov/ct2/show/NCT01799057
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Bronwyn A Kingwell, PhD
Address 0 0
Baker Heart and Diabetes Institute
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Address 0 0
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for scientific queries



Summary Results

For IPD and results data, please see https://clinicaltrials.gov/ct2/show/NCT01799057