VIRTUOSE : Efficiency of Sildenafil on the Absolute Claudication Distance of Peripheral Arterial Disease Patients With Intermittent Claudication.

Experimental design A Phase III, National, Multicentre, Prospective, Randomised, Double Blind, placebo-controlled clinical trial with two parallel groups.

Eligible patients will be randomised in two groups:

• Experimental group Sildenafil citrate 140 mg/day (single morning oral dose of 140 mg) for a total duration of 24 weeks.
• Control group Placebo (single morning oral dose) for a total duration of 24 weeks.

Treatment will be proposed in addition to optimal treatment (Antiplatelet / Direct Oral Anticoagulant + Lipid Lowering Drugs + AT2 antagonists / ACE Inhibitors; unless contra-indicated) + advice to walk.

The experimental drug will be delivered for a 4 weeks treatment period. Phone contact will be carried out at 7 and 14 days focusing on tolerance, compliance and eventual side effects.

First follow up visit at week 4 will focus on tolerance, compliance and side effects. If no major side effect is found, the study drug will be delivered for an additional 8 weeks.

Phone contact will be carried out at 8 weeks focusing on tolerance, compliance and eventual side effects.

Patients will be evaluated at week 12 (second follow-up visit) for persistent or non-persistent indication for revascularization and considered for revascularization if needed. In parallel, attention will be given to tolerance, compliance and eventual side effects. If no major side effect is found, the study drug will be delivered for an additional 12 weeks period.

Phone contact will be carried out at weeks 16 and 20 focusing on tolerance, compliance and eventual side effects.

Third and fourth follow-up visits are scheduled at week 24 (end of treatment) and week 48 (24 weeks after the end of experimental drugs).

Perspectives

• Improving quality of life of patients suffering a chronic debilitating disease is a major issue not only in vascular medicine.
• It is expected that the treatment may help patients change from a vicious circle (Pain > inactivity > disease progression > pain > increased morbi-mortality) to a virtuous circle (no Pain > improved ability for activity > collateral vessel development > slowing of disease progression > decreased morbi-mortality )
• We expect that half of the patients that fulfil inclusion criteria will be sufficiently improved not to require surgery anymore even 24 weeks after the end of the drug as a result of this virtuous circle.

Inclusion criteria

• Patient ≥ 18 years old;
• with peripheral artery disease (ABI ≤ 0.90 or TBI ≤ 0.70 or post-exercise ABI decrease of 18.5% from rest or ABI Exercise TcPO2 with DROPmin ≤ - 15 mmHg) reporting stable limiting claudication despite optimal medical treatment (Antiplatelet / Direct Oral Anticoagulant + Lipid Lowering Drugs + AT2 antagonists / ACE Inhibitors; unless contra-indication) and advice to walk for at least 4 weeks;
• with a walking capacity lower or equal to 500 meters on treadmill;
• affiliation to a social security agency
• Patient who has understood the protocol and signed the consent form to participate.

Exclusion criteria

• Revascularization already decided and scheduled;
• Critical limb ischemia;
• Life threatening disease;
• Contraindication related to Sildenafil:

• Patients treated with nitrates or drugs interfering with the action of sildenafil
• Ongoing treatment by Ritonavir or alpha-blockers
• Hypersensitivity to sildenafil or any of the excipients (lactose monohydrate)
• Recent history of myocardial infarction or stroke < 3 months
• Severe cardiovascular disorders such as unstable angina, severe cardiac failure and cardiomyopathy
• Hypotension (Blood pressure < 90/50 mmHg)
• Severe renal or hepatic failure
• Amblyopia
• Loss of vision in one eye because of Non-arterial ischemic Ophtalmic Neuropathy (NAION)
• Known hereditary degenerative retinal disorders such as retinitis pigmentosa
• Leukemia, Drepanocytosis, Multiple Myeloma
• Pregnancy or breastfeeding;
• Subjects under reinforced protection, deprived of liberty by judicial or administrative decision, hospitalized without consent or admitted to a health or social care establishment for purposes other than research;
• Being in an exclusion period for another clinical study or in an ongoing interventional clinical study.