Reinitiation of Anticoagulation After Temporary Withdrawal of Vitamin K Antagonist (DOSIDO)
Primary Purpose
Atrial Fibrillation, Venous Thromboembolism, Heart Valve Disease
Status
Completed
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Double dose
Sponsored by
About this trial
This is an interventional treatment trial for Atrial Fibrillation focused on measuring warfarin, surgery, management, thromboembolism, bleeding
Eligibility Criteria
Inclusion Criteria:
- Current treatment with warfarin
- Need for temporary interruption for invasive procedure or surgery
Exclusion Criteria:
- Need for post-operative hospitalization more than one day
- Participation in another clinical trial
- No consent given
Sites / Locations
- Thrombosis Service, HHS- General Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Double dose
Usual maintenance dose
Arm Description
Re-initiation with warfarin at twice the usual maintenance dose the first 2 days, then maintenance dose.
Usual maintenance dose from Day 1, i.e. no postoperative loading dose.
Outcomes
Primary Outcome Measures
Proportion of patients with INR back in therapeutic range Day 5 or Day 10
Proportion of patients with INR 2.0-3.0 on Day 5 or Day 10 (day of invasive procedure defined as Day 1)
Secondary Outcome Measures
Thromboembolic events
Objectively verified arterial or venous thromboembolic events
Major bleeding events
Defined by the ISTH criteria of 2010
Minor bleeding events
Any bleeding requiring medical attention but not fulfilling the criteria of Major bleeding
Laboratory parameters of hypercoagulability
Quantitative D-dimer and Thrombin Generation performed in a subset at day of procedure, day 5 and 10 to identify abnormal rise.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01348074
Brief Title
Reinitiation of Anticoagulation After Temporary Withdrawal of Vitamin K Antagonist
Acronym
DOSIDO
Official Title
Phase II Study of Double Versus Single Reinitiation Dose of Warfarin After Interruption for Surgery
Study Type
Interventional
2. Study Status
Record Verification Date
April 2016
Overall Recruitment Status
Completed
Study Start Date
April 2011 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
McMaster University
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
It is not known how to best restart warfarin after temporary withdrawal. Participants will be randomized to two groups. Group 1 will restart warfarin at their usual maintenance dose, group 2 will restart warfarin at double their maintenance dose for two days followed by their usual maintenance dose. The main outcome parameter will be the number of patients who are back in therapeutic INR (international normalized ratio) range 4, and 9 days after restarting anticoagulation with warfarin. Thromboembolic and/or bleeding events will be recorded as additional parameters. These data will be collected by a standardized telephone interview at 1 month. In addition, the investigators will evaluate a possible prothrombotic state by measuring the potential of thrombin generation and D-dimers in the subset of patients visiting HHS-General Hospital for their INR tests.
Detailed Description
We will investigate if it is feasible to use double maintenance dose for the first two administrations of vitamin K antagonists when these drugs were temporarily interrupted and thus keep the time of an increased risk of thromboembolism and duration of "bridging" at a minimum. The control group will consist of patients who resume vitamin K antagonists at their usual maintenance dose. The aim of the study is to establish how to best restart anticoagulation with vitamin K antagonists after temporal withdrawal of these drugs. The main outcome parameter will be the proportion of patients who are back to a therapeutic international normalized ratio (INR) ratio at certain days after restarting vitamin K antagonists. Two additional parameters will be evaluated: Firstly, bleeding and thromboembolic complications will be reported and secondly, a possible prothrombotic state, measured as an elevation of D-dimer, at the initiation of anticoagulation will be evaluated.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation, Venous Thromboembolism, Heart Valve Disease, Surgery
Keywords
warfarin, surgery, management, thromboembolism, bleeding
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
104 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Double dose
Arm Type
Experimental
Arm Description
Re-initiation with warfarin at twice the usual maintenance dose the first 2 days, then maintenance dose.
Arm Title
Usual maintenance dose
Arm Type
No Intervention
Arm Description
Usual maintenance dose from Day 1, i.e. no postoperative loading dose.
Intervention Type
Drug
Intervention Name(s)
Double dose
Other Intervention Name(s)
Loading dose
Intervention Description
For each individual the dose on Day 1 and Day 2 will be twice the one normally taken
Primary Outcome Measure Information:
Title
Proportion of patients with INR back in therapeutic range Day 5 or Day 10
Description
Proportion of patients with INR 2.0-3.0 on Day 5 or Day 10 (day of invasive procedure defined as Day 1)
Time Frame
Day 5-10
Secondary Outcome Measure Information:
Title
Thromboembolic events
Description
Objectively verified arterial or venous thromboembolic events
Time Frame
30 days
Title
Major bleeding events
Description
Defined by the ISTH criteria of 2010
Time Frame
30 days
Title
Minor bleeding events
Description
Any bleeding requiring medical attention but not fulfilling the criteria of Major bleeding
Time Frame
30 days
Title
Laboratory parameters of hypercoagulability
Description
Quantitative D-dimer and Thrombin Generation performed in a subset at day of procedure, day 5 and 10 to identify abnormal rise.
Time Frame
10 days
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Current treatment with warfarin
Need for temporary interruption for invasive procedure or surgery
Exclusion Criteria:
Need for post-operative hospitalization more than one day
Participation in another clinical trial
No consent given
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sam Schulman, MD, PhD
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Thrombosis Service, HHS- General Hospital
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8L 2X2
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
18205763
Citation
Schulman S, El Bouazzaoui B, Eikelboom JW, Zondag M. Clinical factors influencing the sensitivity to warfarin when restarted after surgery. J Intern Med. 2008 Apr;263(4):412-9. doi: 10.1111/j.1365-2796.2007.01913.x. Epub 2008 Jan 16.
Results Reference
background
PubMed Identifier
24837794
Citation
Schulman S, Hwang HG, Eikelboom JW, Kearon C, Pai M, Delaney J. Loading dose vs. maintenance dose of warfarin for reinitiation after invasive procedures: a randomized trial. J Thromb Haemost. 2014 Aug;12(8):1254-9. doi: 10.1111/jth.12613. Epub 2014 Jun 25.
Results Reference
result
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Reinitiation of Anticoagulation After Temporary Withdrawal of Vitamin K Antagonist
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