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CompletedNCT02832570

Sildenafil Efficacy Study on Time Walk From Peripheral Arterial Desease Patients (Stade II) With Arterial Claudication

Etude préliminaire Sur l'efficacité Aigue du Sildenafil Sur le Temps de Marche Chez Les Patients Atteints d'AOMI de Stade II présentant Une Claudication artérielle

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
14 (actual)
Sponsor
University Hospital, Angers · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Efffect of a single dose oral intake of sildenafil Or placebo on the walking capacity on treadmill of PAD patients with claudication

Detailed description

Sildenafil 100mg or Placebo Oral intake 2 hours before the treadmill test Safety and security control throughout the period of drug efficacy (approx 4 hours) Evaluation of maximal walking distance for a constant load treadmill test (3.2 kml/h 10% slope)

Conditions

Interventions

TypeNameDescription
DRUGSildenafil 100mg single oral doseMeasurement of maximal walking distance on a constant load treadmill test (3.12 km/ 10% slope)
DRUGPlacebo, Oral intake single doseMeasurement of maximal walking distance on a constant load treadmill test (3.12 km/ 10% slope)

Timeline

Start date
2016-11-07
Primary completion
2017-10-01
Completion
2017-10-01
First posted
2016-07-14
Last updated
2022-07-29

Source: ClinicalTrials.gov record NCT02832570. Inclusion in this directory is not an endorsement.

Sildenafil Efficacy Study on Time Walk From Peripheral Arterial Desease Patients (Stade II) With Arterial Claudication (NCT02832570) · Clinical Trials Directory