Clinical Trials Directory

Trials / Completed

CompletedNCT01722786

Reversal Agent Use in Patients Treated With Direct Oral Anticoagulants or Vitamin K Antagonists

Prospective, Observational, Non-interventional Open-label Multicenter Registry Regarding the Management of Severe Bleeding and/or Urgent Interventions During Treatment With Direct Oral Anticoagulants or Vitamin K Antagonists

Status
Completed
Phase
Study type
Observational
Enrollment
272 (actual)
Sponsor
Cardioangiologisches Centrum Bethanien · Academic / Other
Sex
All
Age
18 Years – 99 Years
Healthy volunteers
Not accepted

Summary

Patients treated with Vitamin K antagonists (VKA) or direct oral anticoagulants as Rivaroxaban, Apixaban, Edoxaban or Dabigatran, who experience severe bleeding and/or need urgent interventions/operations that cannot wait are included in this registry, or during emergency operations.

Detailed description

The Registry will offer the opportunity to evaluate the effects of reversal agents as PCC, aPCC, rVIIa, specific antidots in e.g. severe bleeding patients treated with oral anticoagulants. By collecting case reports from several university hospitals and clinics, different treatment strategies in clinical practice will be observed and evaluated, and may serve as a comprehensive information resource for the safe management with DOA, but also with the long-term anticoagulation based on coumarin derivatives in the near future. The current objective of this registry is to: 1. Document the clinical course and outcome of various clinical bleeding events associated with DOA or VKA in patients with severe life-threatening bleeding making intervention necessary 2. Document the clinical course and outcome of urgent surgical interventions within 24 hours after admission in patients under DOA or VKA treatment. 3. Characterisation of therapeutic strategies in stopping acute life-threatening bleeding including following agents and methods: 1. blood transfusion, 2. platelet concentrates 3. reversal agents \[e.g. vitamin K, prothrombin complex concentrate (PCC), activated PCC (aPCC), activated factor VII (aVII), fibrinogen concentrate, fresh frozen plasma (FFP)\] 4. specific antidots, e.g. idarucizumab 5. haemodialysis 6. desmopressin 7. tranexamic acid 8. no specific treatment in respect to the above mentioned treatments (e.g. stop of medication and waiting until anticoagulant effect of DOA is decreased).

Conditions

Timeline

Start date
2014-04-01
Primary completion
2018-06-30
Completion
2019-07-09
First posted
2012-11-07
Last updated
2020-07-16

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT01722786. Inclusion in this directory is not an endorsement.