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Register for New Oral Anticoagulants (NOAC)

This study is currently recruiting participants. (see Contacts and Locations)
Verified August 2016 by GWT-TUD GmbH
Information provided by (Responsible Party):
GWT-TUD GmbH Identifier:
First received: April 26, 2012
Last updated: January 19, 2017
Last verified: August 2016
Patients, who are adjusted to a new oral anticoagulant (Dabigatran, Rivaroxaban, Apixaban, Edoxaban) in routine treatment will recorded in this register. Within this register a characterization of patients (with regard to demography and indication) and therapy (with regard to medication, dose and duration) will be done. On basis of defined clinical relevant end points the long-term efficacy and safety will be evaluated.

Anticoagulation Treatment

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Prospective Register Study to Record Safety and Efficacy of New Oral Anticoagulants

Resource links provided by NLM:

Further study details as provided by GWT-TUD GmbH:

Estimated Enrollment: 3500
Study Start Date: November 2011
Estimated Study Completion Date: December 2018
Estimated Primary Completion Date: December 2018 (Final data collection date for primary outcome measure)
in atrial fibrillation
in atrial fibrillation and VTE
in atrial fibrillation and VTE
in atrial fibrillation


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
patients in clinical routine

Inclusion Criteria:

  • indication for treatment with long term anticoagulation
  • initial adjustment or change to nex oral anticoagulant within routine treatment
  • indication for treatment with long term anticoagulation within the register:
  • permanent anticoagulation in arterial fibrillation
  • intended anticoagulation in acute venous thromboembolism for min. 3 months
  • other anticoagulation for min. 3 months within the approved indication

Exclusion Criteria:

  • missing Informed Consent Form
  • missing phone number for telephone follow up
  • contraindication for therapy with new oral anticoagulant (Dabigatran, Rivaroxaban, Apixaban, Edoxaban) according to Summary of Product Characteristics
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its identifier: NCT01588119

Contact: Jan Beyer-Westendorf, MD +49 351 458 ext 3659

Universitätsklinikum Dresden on behalf of GWT-TUD GmbH Recruiting
Dresden, Germany, 01307
Contact: Jan Beyer-Westendorf, MD    0049 0351 458 ext 3659   
Principal Investigator: Jan Beyer-Westendorf, MD         
Sponsors and Collaborators
Principal Investigator: Jan Beyer-Westendorf, MD study site at Universitätsklinikum Dresden on behalf of GWT-TUD GmbH