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Anticoagulant
Vascular dose for Intermittent Claudication
Phase 4
Waitlist Available
Research Sponsored by Science Valley Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 6 months
Awards & highlights
Study Summary
This trial is evaluating if rivaroxaban 2.5 mg BID and aspirin 100 mg OD compared to aspirin alone improves on intermittent claudication distance in PAD patients.
Eligible Conditions
- Intermittent Claudication
- Peripheral Arterial Disease
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 6 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~6 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Absolute claudication distance (ACD) on treadmill
Initial claudication distance (ICD) and the total walking distance (TWD) on 6 MWT
Quality of life Walking Impairment Questionnaire (WIQ)
Secondary outcome measures
Major adverse cardiovascular event
Major adverse events of the limbs
Other outcome measures
Bleeding
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Vascular doseExperimental Treatment1 Intervention
Rivaroxaban 2.5 mg BID and aspirin 100 mg OD for 6 months
Group II: AspirinActive Control1 Intervention
Aspirin 100 mg OD for 6 months
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Acetylsalicylic acid
FDA approved
Find a Location
Who is running the clinical trial?
Science Valley Research InstituteLead Sponsor
8 Previous Clinical Trials
1,243 Total Patients Enrolled
BayerIndustry Sponsor
2,240 Previous Clinical Trials
25,332,689 Total Patients Enrolled
Frequently Asked Questions
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