Very Low Dose Oral Anticoagulation and Thromboembolic and Bleeding Complications (ESCAT III)

This study is currently recruiting participants.
Verified August 2012 by Heart and Diabetes Center North-Rhine Westfalia
Sponsor:
Collaborators:
Klinikum Ludwigshafen
University of Kiel
Information provided by (Responsible Party):
Heart and Diabetes Center North-Rhine Westfalia
ClinicalTrials.gov Identifier:
NCT00528671
First received: September 11, 2007
Last updated: August 9, 2012
Last verified: August 2012

September 11, 2007
August 9, 2012
January 2006
December 2013   (final data collection date for primary outcome measure)
Thromboembolic events, Bleeding events, Survival rates [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
Thromboembolic events, Bleeding events, Survival rates [ Time Frame: 2 years ]
Complete list of historical versions of study NCT00528671 on ClinicalTrials.gov Archive Site
INR values, Percent of INR values in the target range [ Time Frame: 2 years ] [ Designated as safety issue: No ]
INR values, Percent of INR values in the target range [ Time Frame: 2 years ]
Not Provided
Not Provided
 
Very Low Dose Oral Anticoagulation and Thromboembolic and Bleeding Complications
Effects of Very Low Dose Oral Anticoagulation on Thromboembolism and Bleeding Events in Patients With Mechanical Heart Valve Replacement

We aim to investiagte whether very low dose self management of oral anticoagulation is superior to low dose oral anticoagulation in order to prevent bleeding events in patients undergoing mechanuical heart valve replacement.

In mechanical heart valve recipients, self-management of oral anticoagulation can reduce the risk of developing thromboembolic events and improves long-term survival compared with international normalized ratio (INR) control by a general practitioner. Low-dose INR self-management (INR values of 1.8.-2.8 for aortic valve recipients and 2.5 - 3.5 for mitral or double valve recipients) does not increase the risk of thromboembolic events compared to conventional dose INR self-management. Even in patients with a low INR target range, however, the risk of bleeding events is still higher than the risk of thromboembolism. We therefore perform a prospective, randomized trial in 1,800 patients with mechanical heart valve replacement. During the first six postoperative months, low dose INR self-management will be performed by all patients (INR measurement once a week). Thereafter, 600 patients will continue with this treatment regimen, whereas the other 1,200 patients with perform very low dose oral anticoagulation. Out of these 1,200 patients, 600 will perform INR measurement once a week and 600 patients will perform INR measurement twice a week. Patients are followed up for 24 months.

Interventional
Phase 4
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Investigator)
Primary Purpose: Treatment
Mechanical Heart Valve Recipients
  • Drug: phenprocoumon
    The daily phenprocoumon dose administered should achieve an international normalized ratio (INR) of 1.8 - 2.8 for aortic valve recipients and 2.5 - 3.5 for mitral or double valve recipients, INR-self management once a week
  • Drug: phenprocoumon
    The daily phenprocoumon dose administered should achieve an international normalized ratio (INR) of 1.6-2.1 for aortic valve recipients and 2.0 - 2.5 for mitral or double valve recipients, INR self management once a week
  • Drug: phenprocoumon
    The daily phenprocoumon dose administered should achieve an international normalized ratio (INR) of 1.6-2.1 for aortic valve recipients and 2.0 - 2.5 for mitral or double valve recipients, INR self management twice a week
  • Active Comparator: A
    Low dose oral anticoagulation, INR self-management once a week
    Intervention: Drug: phenprocoumon
  • Active Comparator: B
    very low dose oral anticoagulation, INR self-management once a week
    Intervention: Drug: phenprocoumon
  • Experimental: C
    very low dose oral anticoagulation, INR self-management twice a week
    Intervention: Drug: phenprocoumon

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
1800
December 2013
December 2013   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Mechanical heart valve recipients

Exclusion Criteria:

  • Contra-indication to phenprocoumon
  • Ulcerous disease with bleeding tendency,
  • Hypo- or hypercoagulability
  • Dementia
  • Missing informed consent
Both
18 Years to 85 Years
No
Contact: Heinrich Koertke, MD +49 5731 97 2319 hkoertke@hdz-nrw.de
Contact: Armin Zittermann, PhD +49 5731 97 1912 azittermann@hdz-nrw.de
Germany
 
NCT00528671
002
Yes
Heart and Diabetes Center North-Rhine Westfalia
Heart and Diabetes Center North-Rhine Westfalia
  • Klinikum Ludwigshafen
  • University of Kiel
Principal Investigator: Heinrich Koertke, MD Institute of Applied Telemedicine, Heart and Diabetes Center North-Rhine Westfalia, 32545 Bad Oeynhausen, Germany
Heart and Diabetes Center North-Rhine Westfalia
August 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP