Very Low Dose Oral Anticoagulation and Thromboembolic and Bleeding Complications (ESCAT III)
Primary Purpose
Mechanical Heart Valve Recipients
Status
Terminated
Phase
Phase 4
Locations
Germany
Study Type
Interventional
Intervention
phenprocoumon
phenprocoumon
phenprocoumon
Sponsored by

About this trial
This is an interventional treatment trial for Mechanical Heart Valve Recipients focused on measuring phenprocoumon, INR self-management, mechanical heart valve replacement, bleeding, thromboembolism
Eligibility Criteria
Inclusion Criteria:
- Mechanical heart valve recipients
Exclusion Criteria:
- Contra-indication to phenprocoumon
- Ulcerous disease with bleeding tendency,
- Hypo- or hypercoagulability
- Dementia
- Missing informed consent
Sites / Locations
- Heart and Diabetes Center NRW
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Experimental
Arm Label
A
B
C
Arm Description
Low dose oral anticoagulation, INR self-management once a week
very low dose oral anticoagulation, INR self-management once a week
very low dose oral anticoagulation, INR self-management twice a week
Outcomes
Primary Outcome Measures
Thromboembolic events, Bleeding events, Survival rates
Secondary Outcome Measures
INR values, Percent of INR values in the target range
Full Information
NCT ID
NCT00528671
First Posted
September 11, 2007
Last Updated
December 10, 2013
Sponsor
Heart and Diabetes Center North-Rhine Westfalia
Collaborators
Klinikum Ludwigshafen, University of Kiel
1. Study Identification
Unique Protocol Identification Number
NCT00528671
Brief Title
Very Low Dose Oral Anticoagulation and Thromboembolic and Bleeding Complications
Acronym
ESCAT III
Official Title
Effects of Very Low Dose Oral Anticoagulation on Thromboembolism and Bleeding Events in Patients With Mechanical Heart Valve Replacement
Study Type
Interventional
2. Study Status
Record Verification Date
December 2013
Overall Recruitment Status
Terminated
Study Start Date
January 2006 (undefined)
Primary Completion Date
November 2013 (Actual)
Study Completion Date
November 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Heart and Diabetes Center North-Rhine Westfalia
Collaborators
Klinikum Ludwigshafen, University of Kiel
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
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.
Detailed Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mechanical Heart Valve Recipients
Keywords
phenprocoumon, INR self-management, mechanical heart valve replacement, bleeding, thromboembolism
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
1571 (Actual)
8. Arms, Groups, and Interventions
Arm Title
A
Arm Type
Active Comparator
Arm Description
Low dose oral anticoagulation, INR self-management once a week
Arm Title
B
Arm Type
Active Comparator
Arm Description
very low dose oral anticoagulation, INR self-management once a week
Arm Title
C
Arm Type
Experimental
Arm Description
very low dose oral anticoagulation, INR self-management twice a week
Intervention Type
Drug
Intervention Name(s)
phenprocoumon
Intervention Description
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
Intervention Type
Drug
Intervention Name(s)
phenprocoumon
Intervention Description
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
Intervention Type
Drug
Intervention Name(s)
phenprocoumon
Intervention Description
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
Primary Outcome Measure Information:
Title
Thromboembolic events, Bleeding events, Survival rates
Time Frame
2 years
Secondary Outcome Measure Information:
Title
INR values, Percent of INR values in the target range
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Mechanical heart valve recipients
Exclusion Criteria:
Contra-indication to phenprocoumon
Ulcerous disease with bleeding tendency,
Hypo- or hypercoagulability
Dementia
Missing informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Heinrich Koertke, MD
Organizational Affiliation
Institute of Applied Telemedicine, Heart and Diabetes Center North-Rhine Westfalia, 32545 Bad Oeynhausen, Germany
Official's Role
Principal Investigator
Facility Information:
Facility Name
Heart and Diabetes Center NRW
City
Bad Oeynhausen
ZIP/Postal Code
32545
Country
Germany
12. IPD Sharing Statement
Citations:
PubMed Identifier
12970212
Citation
Koertke H, Minami K, Boethig D, Breymann T, Seifert D, Wagner O, Atmacha N, Krian A, Ennker J, Taborski U, Klovekorn WP, Moosdorf R, Saggau W, Koerfer R. INR self-management permits lower anticoagulation levels after mechanical heart valve replacement. Circulation. 2003 Sep 9;108 Suppl 1:II75-8. doi: 10.1161/01.cir.0000089185.80318.3f.
Results Reference
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PubMed Identifier
17184625
Citation
Koertke H, Zittermann A, Wagner O, Koerfer R. Self-management of oral anticoagulation therapy improves long-term survival in patients with mechanical heart valve replacement. Ann Thorac Surg. 2007 Jan;83(1):24-9. doi: 10.1016/j.athoracsur.2006.08.036.
Results Reference
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PubMed Identifier
15976964
Citation
Koertke H, Zittermann A, Mommertz S, El-Arousy M, Litmathe J, Koerfer R. The Bad Oeynhausen concept of INR self-management. J Thromb Thrombolysis. 2005 Feb;19(1):25-31. doi: 10.1007/s11239-005-0937-1.
Results Reference
background
PubMed Identifier
15919283
Citation
Koertke H, Zittermann A, Minami K, Tenderich G, Wagner O, El-Arousy M, Krian A, Ennker J, Taborski U, Klovekorn WP, Moosdorf R, Saggau W, Morshuis M, Koerfer J, Seifert D, Koerfer R. Low-dose international normalized ratio self-management: a promising tool to achieve low complication rates after mechanical heart valve replacement. Ann Thorac Surg. 2005 Jun;79(6):1909-14; discussion 1914. doi: 10.1016/j.athoracsur.2004.09.012.
Results Reference
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Very Low Dose Oral Anticoagulation and Thromboembolic and Bleeding Complications
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