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Clinical Trials/ACTRN12613001304729
ACTRN12613001304729
Recruiting
未知

A multicentre, observational, prospective study of the current practice in major centres in Australia and New Zealand for achieving haemostasis in consecutive patients who present with significant haemorrhage, thromboembolism or urgent surgery whilst on new or established oral anticoagulants

ARES Collaborative0 sites2,000 target enrollmentNovember 22, 2013

Overview

Phase
未知
Intervention
Not specified
Conditions
Significant haemorrhage
Sponsor
ARES Collaborative
Enrollment
2000
Status
Recruiting
Last Updated
6 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 22, 2013
End Date
TBD
Last Updated
6 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
ARES Collaborative

Eligibility Criteria

Inclusion Criteria

  • Patients presenting with significant haemorrhage, thromboembolism or require anticoagulation reversal for urgent surgery and/or a procedure and have taken a NOAC (dabigatran, rivaroxaban, or apixaban) or warfarin within the last 7 days.

Exclusion Criteria

  • Patients who have minor haemorrhage responding to local measures not requiring admission, blood testing or change in anticoagulant management.
  • Patients who are unable to have objective testing for recurrence of thromboembolism.

Outcomes

Primary Outcomes

Not specified

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