Efficacy of Sildenafil on the Morbi-mortality of Peripheral Arterial Diseased Patients With Intermittent Claudication (VALSTAR)

University Hospital, Angers

Status and phase: Withdrawn; Phase 3

Conditions: Peripheral Arterial Occlusive Disease

Treatments: Drug: Placebo oral morning dose; Drug: Sildenafil 100 mg oral morning dose

Study type: Interventional

Funder types: Other

Identifiers

NCT02930811

PHRC-N-2015

Details and patient eligibility

About

Peripheral Arterial Disease (PAD) is a highly debilitating disease that affects 202 million people around the world and about 7 million people in France. Morbi-mortality from cardiovascular events is increased in this population. Intermittent claudication is the most common clinical feature of PAD.

Primary therapeutic approach is medical treatment and advice to walk. Sildenafil, a PDEi type 5, is well tolerated, largely used in impotence and has interesting clinical delay and duration of action in the concept of a potential use in claudication.

For patients agreeing and signing informed consent, randomisation of treatment (placebo/sildenafil) will be done. Treatment will be proposed in addition to usual treatment. The experimental drug will be delivered for a 1 month treatment. First follow up visit at month one will focus on tolerance, compliance and eventual side effects. If no major side effect is found the study drug will then be delivered for an additional 2 months. Patients will be evaluated at month 3 (second follow-up visit) for persistent or non-persistent indication for revascularisation and addressed for revascularization if needed. In parallel focus on tolerance, compliance and eventual side effects will be done. If no major side effect is found, the study drug will be delivered for an additional 3 months treatment. Third and fourth follow-up visit are scheduled at month 6 (end of treatment) and month 9 (3 months after the end of experimental drugs).

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Grade I cat 2 or 3 claudication despite optimal medical treatment
• Reporting a vascular claudication history for at least 3 months
• Able to achieve a walking treadmill test, Walking time on treadmill (3.2km/h, 10% slope) less than 5 minutes
• Having no cons Sildenafil indication
• Must be on optimal medical therapy (ACE Inhibitors / AT2 Antagonist + Antiplatelet + Lipid Lowering drugs) for at least 1 month

Exclusion criteria

• Critical ischemia
• Previous history of myocardial infarction or angina not stabilized
• Amblyopia
• Treated with nitrates (nitroglycerin ...) or drugs interfering with the action of the Sildenafil
• Pregnant woman and woman in labor
• Major Person subject to reinforced protection, deprived of their liberty by judicial or administrative decision, hospitalized without consent or admitted to a health or social establishment for purposes other than research
• Being in an exclusion period for another biomedical study

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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0 participants in 2 patient groups, including a placebo group

Sildenafil

Experimental group

Description:

Single Sildenafil oral morning intake (100mg/day) per day for a total duration of 6 months (Sildenafil 100 mg oral morning dose)

Treatment:

Drug: Sildenafil 100 mg oral morning dose

Placebo

Placebo Comparator group

Description:

Single Placebo oral morning intake per day for a total duration of 6 months (Placebo oral morning dose)

Treatment:

Drug: Placebo oral morning dose