Rivaroxaban for Antiphospholipid Antibody Syndrome

Antiphospholipid Antibody Syndrome Clinical Trial

— RAPS  

Official title:

Rivaroxaban in Antiphospholipid Syndrome Pilot Study: A Multicenter Feasibility Study of Rivaroxaban for Patients With Antiphospholipid Syndrome and Prior Arterial or Venous Thrombosis

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02116036
• Other study ID #: G-13-0002011
• Status: Completed
• Phase: Phase 4
• First received: April 14, 2014
• Last updated: October 16, 2017
• Start date: September 2014
• Est. completion date: September 30, 2017

Study information

• Verified date: October 2017
• Source: St. Joseph's Healthcare Hamilton
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The antiphospholipid antibody syndrome (APS) is a syndrome associated with excessive blood clotting (thrombosis). APS is among the most common cause of heart attack and stroke in patients under the age of 50 and is particularly prevalent in patients with autoimmune conditions. Patients with APS and prior thrombosis require lifelong anticoagulant therapy to prevent recurrent clots; such therapy is currently provided with warfarin. Warfarin requires frequent bloodwork monitoring, and many medications or foods can alter its effect, which can put people either at increased risk for clotting or bleeding. Rivaroxaban is a new mediation that prevents blood clots that does not require bloodwork monitoring and that has fewer interactions. This study is a pilot feasibility study which will: 1) examine our ability to identify 150 eligible APS patients; 2) measure our ability to obtain consent from 135 of these patients; and 3) test our hypothesis that we can obtain 95% compliance with daily rivaroxaban administration. The investigators propose to treat eligible patients with rivaroxaban 20 mg once daily. Patients will be followed for a minimum of one year and their rates of bleeding and thrombosis will be monitored as secondary outcome measures.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 81
• Est. completion date: September 30, 2017
• Est. primary completion date: September 30, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Prior objectively-confirmed venous thrombosis, irrespective of history of arterial thrombosis

• Two or more prior positive APS serological evaluations at least 12 weeks apart

• Current treatment with warfarin administered to achieve an INR of 2.0 to 3.0, rivaroxaban or dabigatran at any dose currently used for secondary prophylaxis of thrombosis, or short term therapeutic dose LMWH (for example, for the treatment of recently diagnosed deep vein thrombosis). Patients not currently receiving anticoagulation but in whom anticoagulation is mandated, may also be enrolled if a 20 mg rivaroxaban dose would be appropriate

Exclusion Criteria:

• Prior recurrent thrombosis while taking warfarin with a demonstrated INR of 2.0 to 3.0, or prior recurrent thrombosis while receiving dabigatran or rivaroxaban

• History of isolated arterial thrombosis (no history of venous thrombosis) pending CTA approval by Health Canada

• Need for continued treatment with both aspirin (irrespective of dose) AND clopidogrel

• Pregnancy or planned pregnancy during the study period; women who may become pregnant will be required to utilize reliable contraceptive measures while on study drug

• Chronic kidney disease with calculated GFR < 30mL/min

• Geographic inaccessibility

• Age < 18 years

• Inability or failure to provide informed consent

Related Conditions & MeSH terms

• Antiphospholipid Antibody Syndrome
• Antiphospholipid Syndrome
• Syndrome

Intervention

Drug:
• Rivaroxaban

Locations

Country	Name	City	State
Canada	University of Alberta Hospital	Edmonton	Alberta
Canada	Queen Elizabeth II Hospital	Halifax	Nova Scotia
Canada	Hamilton General Hospital	Hamilton	Ontario
Canada	St. Joseph's Healthcare Hamilton	Hamilton	Ontario
Canada	Jewish General Hospital	Montreal	Quebec
Canada	The Ottawa Hospital	Ottawa	Ontario

Sponsors (8)

Lead Sponsor	Collaborator
St. Joseph's Healthcare Hamilton	Bayer, Hamilton Health Sciences Corporation, Heart and Stroke Foundation of Canada, Jewish General Hospital, Queen Elizabeth II Health Sciences Centre, The Ottawa Hospital, University of Alberta

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Feasibility of identification for enrolment	The investigators define success as the ability to identify 150 eligible patients at 6 clinical centres over 18 months.	18 months
Primary	Feasibility of Consent	The investigators define success as a consent rate of 90% (thus, if we identify 150 patients, at least 135 will provide consent).	18 months
Primary	Compliance	The investigators define success as a patient missing fewer than 5% of days with pill administrations, as measured by pill counts.	Minimum of one year for all subjects
Secondary	Bleeding	The investigators will collect and report the rates of minor bleeding (clinically apparent bleeding that does not meet the criteria for major), and major and fatal bleeding. Major bleeding will be defined by International Society of Thrombosis and Hemostasis criteria.	Minimum of one year for all subjects
Secondary	Thrombosis	The investigators will collect and report the rates of objectively-confirmed venous and arterial thrombosis.	Minimum of one year for all subjects