Reduced Cardiovascular Morbi-mortality by Sildenafil in Patients With Arterial Claudication
Primary Purpose
Peripheral Arterial Disease
Status
Unknown status
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Sildenafil
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Peripheral Arterial Disease focused on measuring Claudication, Maximal walking distance, Morbi-mortality
Eligibility Criteria
Inclusion Criteria:
- ABI<0.90
- Vascular type claudication
- stable walking impairment for at least 3 months
- Optimal cardiovasc treatment (Anti-platelet, HMGCoA-Inh, ACE-Inh or AT2 inh)
- Age > 30 years
Exclusion Criteria:
- Refuse to participate
- Administrative protection
- Severe renal (clearance < 30 ml/min) or hepatic (Child-Pugh C) failure
Sites / Locations
- Centre hospitalier universitaire
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Treated group
Control group
Arm Description
Sildenafil, oral, 100mg per day
placebo oral
Outcomes
Primary Outcome Measures
Morbi-mortality : combined criterion (Cardiovascular fatal and non fatal event Improvement of 1 stage)
Secondary Outcome Measures
Quality of life Questionnaire
Safety and secondary effects (Headache, Hypotension) (Proportion of Participants with Adverse Event)
Proportion of Participants with Adverse Events (sildenafil vs. placebo)
Walking capacity (treadmill test)
treadmill test
Proportion of revascularized patients
Revascularisation
Full Information
NCT ID
NCT02387450
First Posted
March 2, 2015
Last Updated
March 12, 2015
Sponsor
University Hospital, Angers
1. Study Identification
Unique Protocol Identification Number
NCT02387450
Brief Title
Reduced Cardiovascular Morbi-mortality by Sildenafil in Patients With Arterial Claudication
Official Title
Reduction de la Morbi-mortalité Cardiovasculaire Chez l'artériopathe Claudicant Par le Sildenafil
Study Type
Interventional
2. Study Status
Record Verification Date
March 2015
Overall Recruitment Status
Unknown status
Study Start Date
September 2015 (undefined)
Primary Completion Date
June 2017 (Anticipated)
Study Completion Date
September 2017 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Angers
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Sildenafil has shown potential effects both on vasodilator mechanisms and as an inhibitor of the NO/GMPc Pain activation. The investigators aim at estimating the benefit of sildenafil in term of morbi-mortality in patients with arterial claudication on a multicenter prospective double blind study.
Detailed Description
Eligible patients will ask to participate after oral and written information. Evaluation of walking capacity (self reported and treadmill measured), co-morbid condition and quality of life (WELCH, SF-36, Edinburg) will be performed at inclusion, after the first dose and at 3 months of oral treatment through sildenafil 100mg/day or placebo from inclusion to 3 months.
Indication for revascularisation will be evaluated at 3 months according to symptoms and walking capacity according to the Rutherford classification.
Primary endpoint is the proportion of patients showing either a fatal events (cardio-vascular or noncardiovascular) or hospitalisation for non fatal cardiovascular events at 6 and 9 months follow up from inclusion.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Arterial Disease
Keywords
Claudication, Maximal walking distance, Morbi-mortality
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderOutcomes Assessor
Allocation
Randomized
Enrollment
400 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Treated group
Arm Type
Active Comparator
Arm Description
Sildenafil, oral, 100mg per day
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
placebo oral
Intervention Type
Drug
Intervention Name(s)
Sildenafil
Other Intervention Name(s)
Viagra or revatio
Intervention Description
100 mg per day
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo with same presentation as the active drug
Primary Outcome Measure Information:
Title
Morbi-mortality : combined criterion (Cardiovascular fatal and non fatal event Improvement of 1 stage)
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Quality of life Questionnaire
Time Frame
3, 6 and 9 months
Title
Safety and secondary effects (Headache, Hypotension) (Proportion of Participants with Adverse Event)
Description
Proportion of Participants with Adverse Events (sildenafil vs. placebo)
Time Frame
3, 6 and 9 months
Title
Walking capacity (treadmill test)
Description
treadmill test
Time Frame
3, 6 and 9 months
Title
Proportion of revascularized patients
Description
Revascularisation
Time Frame
6 and 9 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
ABI<0.90
Vascular type claudication
stable walking impairment for at least 3 months
Optimal cardiovasc treatment (Anti-platelet, HMGCoA-Inh, ACE-Inh or AT2 inh)
Age > 30 years
Exclusion Criteria:
Refuse to participate
Administrative protection
Severe renal (clearance < 30 ml/min) or hepatic (Child-Pugh C) failure
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
pierre ABRAHAM, MD, PhD
Phone
+33 241353689
Email
piabraham@chu-angers.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
pierre Abraham, MD, PhD
Organizational Affiliation
University Hospital in Angers
Official's Role
Principal Investigator
Facility Information:
Facility Name
Centre hospitalier universitaire
City
Angers
ZIP/Postal Code
49933
Country
France
12. IPD Sharing Statement
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Reduced Cardiovascular Morbi-mortality by Sildenafil in Patients With Arterial Claudication
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