Secondary Prevention of VTE in Patients With Cancer and Catheter-Related Upper Extremity Deep Vein Thrombosis

PHASE4RecruitingINTERVENTIONAL
Enrollment

330

Participants

Timeline

Start Date

December 19, 2024

Primary Completion Date

October 31, 2029

Study Completion Date

October 31, 2029

Conditions
Venous ThromboembolismCancerUpper Extremity Deep Vein ThrombosisCatheter-Related Infections
Interventions
DRUG

Apixaban

Apixaban is Health Canada approved for routine treatment and secondary prevention of VTE. Upon enrollment and during follow-up, patients will be managed with a prophylactic dose of apixaban (2.5 mg orally twice daily) as long as either a CVC or active cancer is present. Apixaban will be stopped at the time of CVC removal and when cancer is in remission. Patients will be instructed to contact the study team when their CVC is removed (to determine if apixaban should be continued, based on cancer status at the time), or any thrombotic or bleeding concerns were to occur in between visits. The investigators will record loss to follow-up, drop out, or death during the study.

Trial Locations (1)

K1H 8L6

RECRUITING

The Ottawa Hospital, Ottawa

All Listed Sponsors
lead

Ottawa Hospital Research Institute

OTHER