PAD_RIV_CLI: Influence of Rivaroxaban for Intermittent Claudication and Exercise Tolerance in Patients With Symptomatic PAD
Study Details
Study Description
Brief Summary
The aim of the conducted research is to evaluate the protective effect of rivaroxaban (trade name of the Xarelto medicinal product), administered together with acetylsalicylic acid (ASA), in comparison with the effectiveness of using ASA alone, in relation to the distance of claudication and exercise tolerance in patients with PAD over a period of 3 months. At present, COMPASS results show that rivaroxaban vascular dose (2.5 mg twice daily) in combination with ASA (75-100 mg once daily) provides more effective cardiovascular protection (defined as cardiovascular death, vascular, myocardial infarction and stroke) compared to ASA alone. So far, however, no scientific studies have been carried out into account the effect of the drug on the progress of PAD and exercise tolerance in patients.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
Detailed Description
EXISTING KNOWLEDGE AND MAIN ASSUMPTIONS OF THE PROJECT.
Atherosclerosis is the most common cause of peripheral artery disease (PAD). The first symptom of PAD is intermittent claudication (IC), which is characterized by the occurrence of pain, cramps, numbness, and discomfort in the lower limb muscles. They gradually intensify while walking, forcing the patient to stop. The symptoms are caused by continuous, specific physical effort and quickly disappear when it is stopped. The reduction of the possibility of walking leads to a decrease in the quality of life of patients and adds to other dangerous consequences of atherosclerosis, increased risk of cardiovascular incidents (myocardial infarction (MI), stroke, acute lower limb ischemia, Micker M et al. 2006).
Pharmacological treatment of patients with IC is aimed at modifying cardiovascular risk factors and improving the quality of life by alleviating pain and prolonging the claudication distance (Goszcz et al., 2009).
- New possibilities for the pharmacotherapy of patients with symptomatic PAD.
According to the adopted TASC (The Trans Atlantic Inter-Society Consensus), and its TASC II supplement concerning aspects of management and treatment of patients with chronic limb ischemia (CLI), drugs used in PAD are divided into nine groups: those with documented clinical effect used in IC (cilostazol and naphthydrofuryl), drugs with probable clinical effect used in IC (carnitine and propyl-L-carnitine), lipid-lowering drugs (statins), drugs with insufficiently proven clinical effects (penthoxyphilin), anticoagulants, L-arginine, 5-hydroxytryptamine (ketanserin) antagonism, buflomedil, and defibrotide.
- Antiplatelet drugs
Antiplatelet drugs are used to prevent thrombotic complications in the course of myocardial infarction, stroke, and thrombi in peripheral arteries. Acetylsalicylic acid (ASA, aspirin) at doses of 75-325 mg per day, ticlopidine at doses of 250 mg twice a day, and clopidogrel at doses of 75 mg once a day (CAPRIE, 1996) are proven to be effective in PAD patients. Recently there have been reports of beneficial effects of policosanol (a cholesterol-lowering drug with an antiplatelet effect), which prolongs the claudication distance after 10 weeks of treatment (10 mg once a day; clinical trial). The results of ASA (100 mg daily) were however inconclusive (Illnait et al., 2008).
The group of new antiplatelet drugs, used in PAD patients, includes rivaroxaban (trade name Xarelto), which in a vascular dose (2.5 mg twice a day) combined with ASA (75-100 mg once a day) provides more effective cardiovascular protection (defined together as cardiovascular death, MI and stroke) compared to ASA alone in the COMPASS study (Anand SS et al. 2018; Olinic DM et al. 2018; Connolly SJ, 2018).
Other studies with the acronyms MACE and MALE, conducted in the PAD patients of nearly 5,000 cases in total, confirm that the use of rivaroxaban provides comprehensive vascular protection in PAD. The former showed a 28% reduction in the risk of cardiovascular death/myocardial infarction/brain stroke, the latter a 44% reduction in the risk of acute lower limb ischemia and a 46% reduction in the risk of acute/chronic limb ischemia and a 70% reduction in the risk of large amputations. This is the only anticoagulant that, in combination with ASA, reduces mortality in patients with coronary artery disease (CAD) and PAD. At the same time, Xarelto, in a vascular dose, in combination with ASA, does not cause a significant increase in the risk of major bleedings compared to ASA itself. So far, this drug has not been tested in the context of prolongation of the claudication distance.
Rivaroxaban inhibits the formation of thrombin and clots by directly inhibiting factor Xa (activated factor X), thus preventing the transformation of prothrombin into thrombin and interrupting the final common path of the blood clotting cascade. This drug competitively inhibits factor Xa with 10,000 times the selectivity of related serine proteases such as thrombin and factors VIIa, IXa, and XIa. Numerous experimental data suggest the role of clotting system components in regulating atherosclerosis progression (Borensztajn K et al., 2008; Borissoff et al., 2009; Platek and Szymanski, 2019). Various factors of the coagulation cascade mediate these activities, and the broadest spectrum of action concerns the effect of the complex of factor Xa and thrombin precisely.
Scientific research confirms the pleiotropic effects of rivaroxaban on the cardiovascular system. However, most of the currently available observations come from basic research whose results need to be confirmed in clinical trials. Among the planned clinical trials that may establish pleiotropic rivaroxaban actions, the PRE -FER-AF study (PREvention oF thromboembolic events - European Registry in Atrial Fibrillation) is mentioned as the most important. This study aims to determine the efficacy of oral anticoagulants other than vitamin K antagonists (NOAC) in preventing endothelial dysfunction and atherosclerosis progression in patients with atrial fibrillation. However, it will not provide information on the effect of the drug on the progress of PAD or exercise tolerance.
- The objective
The aim of the study is to assess the protective efficacy of rivaroxaban, administered together with ASA, in comparison with the efficacy of ASA alone, with respect to intermittent claudication and exercise tolerance in patients with PAD over a 3-month period.
- Type of study
Prospective, observational, unblinded (open), randomized, case-control, single-centre.
- Description of the study group (age, gender, health status, size of the group).
The study will include PAD patients in Fountaine stage II, hospitalized in the Clinical Hospital of Transfiguration (Department of Vascular and Endovascular Surgery, Angiology and Phlebology of the Poznan University of Medical Sciences), monitored in the adjacent Outpatient Clinic or referred by cooperating physicians who will use a different protocol of anticoagulation pharmacotherapy to prevent thrombotic events. The recommended pharmacotherapy does not exceed the standard of treatment in patients with PAD.
5.1 Size of the study group. At least 60 PAD patients will be included. The collection and observation of the study group will take place until the scientific goal of the study is achieved. Therefore the possibility of increasing the recruitment of patients for the study is assumed up to 100 patients.
5.2 Characteristics of the study group. The inclusion/exclusion criteria, medical history, and cardiovascular risk factors will be examined. Then patients will be subjected to objective assessment of exercise tolerance, assessment of claudication distance, implementation of anticoagulation pharmacotherapy protocol and prospective study protocol. Venous blood samples (9-18 ml), and capillary blood for diagnostic, biochemical, and molecular analysis will be collected. Costs will be shared between cooperating centers.
5.3 Pharmacotherapy. Vascular doses of drugs will be used in one group: 1 x/day ASA 75-100 mg and in the other: 1 x/day ASA 75-100 mg + 2 x/day 2.5 mg Xarelto.
- Methods The general study plan assumes up to 5 visits of the patient to the cooperating centers during the study. First visit to the Hospital-Outpatient Clinic for recruitment (interview with the patient, obtaining written consent, patient registration, the appointment of the next visit, and optionally USG-Doppler of arteries). Second visit to the hospital's blood collection point for fasting blood tests (blood collection for tests and optionally USG-Doppler of arteries). During the third and fourth visits at University of Physical Education treadmill tests with additional tests (ECG, ABI, TCPO2 measurements before and after treadmill test, as well as biochemical evaluation of effort tolerance and subjective assessment of effort using Borg scale) will be performed. During third visit, randomization will also be done. The fourth visit will be scheduled after three months. Then data will be collected and analyzed. During the fifth visit, USG-Doppler of arteries will be performed, and a patient recommendation will be issued.
6.1 Clinical characteristics of the studied population. The following clinical data will be collected for the study: a) results of aortic and lower limb arteries imaging, b) results of heart function tests, c) assessment of the occurrence and severity of atherosclerotic lesions in blood vessels (including: ABI, IMT,TcPO2 value), d) results of fasting venous blood laboratory tests including blood lipid parameters, glucose metabolism, liver and renal function, homocysteine, folic acid, peripheral blood morphology, blood coagulation parameters, e) blood pressure parameters, f) results of virological and bacteriological tests, g) anthropometric data, h) smoking status, i) pharmacotherapy j) coexisting diseases,
- pain, l) family history of cardiovascular disease and cancer.
6.2 Treadmill test. The effect of pharmacotherapy will be assessed based on the treadmill test that will be carried out according to Gardner protocol (Gardner et al., 1991). Patients will march on a treadmill at a constant speed of 3.2 km/h. The initial angle of the slope will be 0% and will be raised by 2% every 2 minutes. The test will be carried out in the Laboratory of Functional Testing of the Department of Physiology and Biochemistry of the University of Physical Education in Poznan, with no contraindications (based on the result of an ECG). The subjects will be tested at each of the test dates to assess the claudication distance on the Katana S30p medical treadmill (Lode BV, Netherlands) (Mika et al. 2009). The total time of each test will not exceed 16 minutes 40 seconds, and the regeneration time will be at least 5 minutes. When the patient reports pain (i.e., grade 2 on a subjective pain assessment scale), the time of occurrence of the claudication will be recorded, from which the claudication distance (DGCH) will be estimated. The test will be interrupted when very severe pain occurs that prevents further walking (step 5 corresponding to maximum walking time), and the maximum walking time will then be recorded. The maximum walking time will be used to estimate the maximum walking distance (DGMAX). Once the treadmill tests have been completed, patients will undergo a control ECG examination to exclude ischemic changes in the heart muscle and cardiac arrhythmias.
6.3. Evaluation of exercise tolerance. The assessment of exercise tolerance will be carried out based on the duration of the effort and questionnaires (Borg scale; Smarż et al. 2015), and biochemical exponents (metabolic equivalent MET-s will be estimated; Bires AM et al., 2013). At rest and 3 minutes after the exercise, the intensity of metabolic exercise acidosis will be assessed based on lactate concentration in capillary blood taken from the fingertip. At the same time, venous blood will also be collected for other biochemical tests, including gasometry.
6.4 Length of observation. The effects of the treatment will be assessed within three months, but the observation period can be extended to a maximum of 12 months.
6.5 End points of the study. The main endpoints of this study and the complications have been developed in accordance with the results adopted in the COMPASS study. Parameters related to the effects of the treadmill test were added.
6.6 Biological material and its use. Blood samples will be collected for further analysis and DNA extraction. The concentration of lactate will be tested using EDGE Blood Lactate Test Strip, ApexBio, (Taiwan). The level of selected blood biomarkers will be assessed by the immunoenzymatic method (ELISA) for proteins, and TaqMan tests or corresponding methods for circulating miRNAs and DNA.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Rivaroxaban [2.5 mg] + Aspirin Drug: Rivaroxaban 2.5 mg twice daily, tablet Drug: Aspirin 75-100 mg once daily, tablet |
Drug: Rivaroxaban
Rivaroxaban 2.5 MG (Xarelto) twice daily, tablet
Other Names:
Drug: Aspirin
Aspirin 75-100 mg once daily, tablet
Other Names:
|
| Active Comparator: Aspirin Drug: Aspirin 75-100 mg once daily, tablet |
Drug: Aspirin
Aspirin 75-100 mg once daily, tablet
Other Names:
|
Outcome Measures
Primary Outcome Measures
- Number of Participants Diagnosed with Stroke at 3 Months [3 months]
Number of participants diagnosed with ischemic or hemorrhagic stroke
- Number of Participants Diagnosed with Myocardial Infarction (MI) at 3 Months [3 months]
Number of participants diagnosed with myocardial infarction
- Number of Participants who Died from Cardiovascular Causes at 3 Months [3 months]
Number of participants who died because of Cardiovascular causes
- Number of Participants who Died from Any Cause at 3 Months [3 months]
Number of Participants who died for any reason not related to accidents.
- Number of Participants Diagnosed with Acute Limb Ischaemia (ALI) at 3 Months [3 months]
Number of participants diagnosed with acute limb ischaemia definied as limb threatening ischaemia with evidence of acute arterial obstruction by radiological criteria or a new pulse deficit leading to an intervention (ie, surgery, thrombolysis, peripheral angioplasty, or amputation.
- Number of Participants Diagnosed with Major Limb Amputation (AMI) at 3 Months [3 months]
Number of participants diagnosed with major limb amputation defined as amputations due to a vascular event above the forefoot, or defined as minor amputation if involving the forefoot and digits.
- Change From Baseline in the Distance of Intermittent Claudication (Δ Dch) at 3 Months [3 months]
Change in the distance of intermittent claudication in the test according to Gardner's protocol
- Change From Baseline in the Maximal Distance of Intermittent Claudication (Δ Dmax) at 3 Months [3 months]
Change in the maximal distance of intermittent claudication in the test according to Gardner's protocol
Other Outcome Measures
- Number of Participants Diagnosed with Fatal Bleeding (FB) at 3 Months [3 months]
Number of participants diagnosed with bleeding that directly results in death within 7 days after its occurrence
- Number of Participants Diagnosed with Non-Fatal Symptomatic Intracranial Haemorrhage (IH) at 3 Months [3 months]
Number of participants diagnosed with non-fatal symptomatic intracranial haemorrhage.
- Number of Participants Diagnosed with Non-Fatal, Non-Intracranial Haemorrhage (Non-IH) Symptomatic Bleeding at 3 Months into a critical organ [3 months]
Number of participants diagnosed with non-fatal, non-intracranial haemorrhage symptomatic bleeding into a critical organ
- Number of Participants Diagnosed with Other Major Bleeding at 3 Months [3 months]
Number of participants diagnosed with other major bleeding defined as surgical site bleeding, surgical site bleeding, that requires reoperation or bleeding leading to hospitalization
- Number of Participants Diagnosed with Fatal or Symptomatic Bleeding into a Critical Organ at 3 Months [3 months]
Number of participants diagnosed with fatal or symptomatic bleeding into a critical organ
- Number of Participants Diagnosed with Major Bleeding according to ISTH criteria at 3 Months [3 months]
Number of participants diagnosed with major bleeding according to modified the International Society on Thrombosis and Haemostasis (ISTH) criteria for major bleeding, defined as the composite of bleeding that was fatal, symptomatic bleeding into a critical organ, surgical site requiring reoperation, or requiring hospitalization (including presentation to an acute care facility without an overnight stay).(ISTH)/Scientific and Standardization Committee (SSC) definitions
- Number of Participants Diagnosed with Minor Bleeding at 3 Months [3 months]
Number of participants diagnosed with clinically relevant minor bleeding defined as an acute or subacute clinically overt bleed that does not meet the criteria for a major bleed but prompts a clinical response, in that it leads to at least one of the following: 1) a hospital admission for bleeding, or 2) a physician-guided medical or surgical treatment for bleeding, or 3) a change in antithrombotic therapy (including interruption or discontinuation of study drug).
- Number of Participants Diagnosed with Gastrointestinal Bleeding at 3 Months [3 months]
Number of participants diagnosed with gastrointestinal bleeding.
- Number of Participants Diagnosed with Intracranial Bleeding at 3 Months [3 months]
Number of participants diagnosed with intracranial bleeding
- Number of Participants Diagnosed with Genitourinary Bleeding at 3 Months. [3 months]
Number of participants diagnosed with genitourinary bleeding.
- Number of Participants Diagnosed with Ocular Bleeding at 3 Months. [3 months]
Number of participants diagnosed with ocular bleeding.
- Number of Participants Diagnosed with Skin Bleeding at 3 Months. [3 months]
Number of participants diagnosed with skin bleeding.
- Number of Participants Diagnosed with Respiratory Bleeding at 3 Months. [3 months]
Number of participants diagnosed with respiratory bleeding.
- Number of Participants Diagnosed with Other Bleeding at 3 Months. [3 months]
Number of participants diagnosed with bleeding other than: gastrointestinal, intracranial, genitourinary, ocular, skin, respiratory.
Eligibility Criteria
Criteria
Inclusion Criteria:
- PAD, the Fontaine classification II
Exclusion Criteria:
-
Severe heart failure with known ejection fraction <30% or NYHA class III or IV symptoms
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High risk of bleeding
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Stroke with one month or any history of hemorrhaging or lacunar stroke
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Estimated glomerular filtration rate <15 ml/ml
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Need for dual antiplatelet therapy, other non-aspirin antiplatelet therapy/, oral anticoagulant therapy/
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The known non-cardiovascular disease that is associated with poor prognosis (i.n, metastatic cancer)
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History of hypersensitivity or known contraindication for rivaroxaban, aspirin
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Systemic treatment with strong inhibitors of CYP 3A4 as well as p-glycoprotein or strong inducers of CYP 3M
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Any known hepatic disease associated with coagulopathy
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Concurrent participation in another study with an investigational drug
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Known contraindication to any study-related procedures* Concerns: Absolute contraindications to an exercise test
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Respiratory failure
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BMI above or equal 40
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Musculoskeletal dysfunction preventing walking (e.g. amputations)
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Poznan University of Medical Sciences
- Poznan University of Physical Education
Investigators
- Principal Investigator: Zbigniew Krasiński, Prof, MD, Poznan University of Medical Sciences
- Study Director: Ewa Strauss, PhD, Poznan University of Medical Sciences
Study Documents (Full-Text)
More Information
Additional Information:
Publications
None provided.- 132/20