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Phase 2 N=20 Randomized Prevention

Pilot Study to Examine the Use of Rivaroxaban After Angioplasty for Critical Limb Ischemia

Critical Limb Ischemia

Enrolled (actual)
20
Serious AEs
0.0%
Results posted
Nov 2019
Primary outcome: Primary: Reintervention, Above Ankle Amputation and Restenosis (RAS) — 7; 4 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
rivaroxaban plus aspirin (Drug); clopidogrel plus aspirin (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Ottawa Hospital Research Institute
Primary completion
Jun 2017

Outcome Measures

OutcomeResultp-value
PRIMARY
Reintervention, Above Ankle Amputation and Restenosis (RAS)
7; 4
SECONDARY
Number of Participants With 2 Class Improvement on the Rutherford Scale
5; 8
SECONDARY
Event-free Survival
4; 4
SECONDARY
Overall Survival
11; 9
SECONDARY
The Number of Patients Requiring Target Lesions Revascularization Between Day 1 and the Final Visit (TLR)
2; 1
SECONDARY
TVR
2; 1
SECONDARY
Peri-procedure Death
0; 0
SECONDARY
MACE
0; 0
SECONDARY
Major Bleeding
0; 0
SECONDARY
Minor Bleeding
0; 1
SECONDARY
Biomarkers

Summary

Background: Up to 10% of patients with peripheral arterial disease (PAD) will develop critical limb ischemia (CLI) which is a decrease of blood flow in the arteries of the limb. CLI results in resting pain, ulcers, gangrene, and limb loss. The outcome for patients with CLI is poor. Within 3 months of onset, 12% of patients will require an amputation (removal of part of the limb) and 9% will die of major cardiovascular events (heart attack or stroke). Percutaneous angioplasty (PTA), a procedure used to open the blockages in blood flow, has become the first-line treatment for CLI given its effectiveness, lower cost, and lower risk of complications. However, 40% of patients will have re-narrowing of the arteries (restenosis) following the PTA procedure. This is thought to happen in part due to build up of blood cells called platelets which can also lead to the formation of blood clots. In order to try to avoid this problem, most patients are prescribed a combination of two blood thinning medications, acetylsalicylic acid (ASA or aspirin) and clopidogrel (the brand name is Plavix). The purpose of this study is to determine if a new blood thinner called rivaroxaban, given in combination with aspirin, would be more effective in preventing re-narrowing of the arteries than the current standard of care (aspirin and clopidogrel). Rivaroxaban is a pill and does not require blood test monitoring. It has been approved by Health Canada for use in prevention of blood clots in patients undergoing hip or knee surgery and to treat patients with blood clots in their legs and lungs. Low dose aspirin has been approved for reducing the risk of heart attacks and strokes. These medications have not been tested together in patients for prevention of re-narrowing of their arteries This is a pilot study conducted at one center, The Ottawa Hospital. It is a Phase 2 open label randomized controlled trial. Following the PTA procedure, once all inclusion/exclusion criteria are met, the participant will be randomized into one of two groups: 1. Rivaroxaban 2.5 mg BID X 90 days plus ASA 81 mg daily OR 2. Clopidogrel 75 mg daily X 90 days plus ASA 81 mg daily Visits will occur at 7 days, 30 days, 90 days, 6 months and 12 months. Participants will be followed for 12 months (± 14 days) in total. All adverse events will be collected for the duration of the study.

Eligibility Criteria

Inclusion Criteria

  • Written informed consent.
  • Infra-inguinal PAD presenting as CLI defined as a Rutherford category of 3, 4, or 5
  • More than 50% stenosis in the target infrainguinal vessel
  • Good candidates for PTA using POBA (plain old balloon angioplasty) with or without stenting defined as TASC a and b lesions.

Exclusion Criteria

  • Rutherford scale of 0,1,2 or 6
  • Acute limb-threatening ischemia (e.g. embolic disease)
  • Previous infrainguinal bypass or PTA procedures of the affected leg
  • Hybrid procedures
  • Creatinine clearance 1.5; Hbg 3ULN)
  • Childbearing potential without proper contraceptive measures, pregnancy or breast feeding
  • Drug addiction or alcohol abuse within 12 months before the randomization visit
  • Systemic treatment with strong CYP 3A4 and P-glycoprotein inhibitors : such as ketoconazole, itraconazole, posaconazole, or ritonavir
  • Known allergy or hypersensitivity to any component of rivaroxaban, ASA or clopidogrel
  • Need for long term anticoagulation or double antiplatelet agents other than PAD such as atrial fibrillation, heart valve replacement, acute coronary syndrome, stroke or venous thromboembolism
  • Anticipated need for chronic (> 4 weeks) therapy with non-steroidal anti-inflammatory drugs.
  • Concomitant treatment with any other anticoagulant, including oral anticoagulants, such as warfarin, dabigatran, apixaban, except under circumstances of switching therapy to or from study treatment.
  • Inability to adhere to protocol.
  • Severe concomitant condition or disease (e.g. life expectancy <6 months secondary to cancer, advanced liver disease or dementia)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02260622). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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