search
Back to results

Early Identification of Warfarin Maintenance Dosage

Primary Purpose

Atrial Fibrillation

Status
Completed
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
Calculate warfarin dose using demographic/genetic algorithm
Sponsored by
University of Padova
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Atrial Fibrillation focused on measuring Warfarin, Dose, Pharmacogenetic, INR

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age >18 years
  • Indication to warfarin with INR between 2.0 and 3.0

Exclusion Criteria:

  • Pregnancy
  • Drug interactions
  • Basal INR > 1.2

Sites / Locations

  • Thrombosis Centre

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

pharmacogenetic warfarin dose

Arm Description

Warfarin maintenance dose on the basis of demographic/pharmacogenetic data

Outcomes

Primary Outcome Measures

International Normalized Ratio (INR)
Number of INR outside the therapeutic range (INR 2.0-3.0)

Secondary Outcome Measures

Number of changes in warfarin dosage
Difference between predicted and actual warfarin maintenance dose
Thromboembolic and Bleeding complications

Full Information

First Posted
August 6, 2010
Last Updated
October 21, 2012
Sponsor
University of Padova
search

1. Study Identification

Unique Protocol Identification Number
NCT01178034
Brief Title
Early Identification of Warfarin Maintenance Dosage
Official Title
Early Identification of Warfarin Maintenance Dose in Patients With Atrial Fibrillation: a Randomized Trial Evaluating a New Genotype-based Versus Usual Care Initiation of Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
October 2012
Overall Recruitment Status
Completed
Study Start Date
October 2009 (undefined)
Primary Completion Date
October 2012 (Actual)
Study Completion Date
October 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Padova

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Initiation of warfarin therapy is problematic. The investigators goal was to evaluate if a new demographic/pharmacogenetic algorithm is better than a usual algorithm based on INR value at day five after four days of 5 mg/day warfarin. To this end patients with atrial fibrillation starting warfarin are randomized in two arms.
Detailed Description
The objective of this randomized study is to evaluate the accuracy of a new demographic/pharmacogenetic as compared to usual warfarin dosing algorithm in predicting warfarin maintenance dose. In patients with atrial fibrillation starting anticoagulation, the loading dose of warfarin in the tested group is calculated on the basis of VKORC1 genotype and patient's body weight.The second day warfarin maintenance dose is calculated on the basis of surface area and CYP2C9, CYP4F2 e VKORC1 genotype. In the usual care group the maintenance dose at day 5 is calculated on the basis of a published algorithm (Pengo V, Am J Cardiol 2001). INR is checked on day 0, 5, 7, 9, 12, 15 and 19. Primary end-point of the trial is the number of INR outside the therapeutic range of 2.0 to 3.0. Secondary end-points are the number of changes in dose prescription, the difference between predicted and actual warfarin maintenance dose and thrombotic and bleeding events.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Atrial Fibrillation
Keywords
Warfarin, Dose, Pharmacogenetic, INR

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
180 (Actual)

8. Arms, Groups, and Interventions

Arm Title
pharmacogenetic warfarin dose
Arm Type
Experimental
Arm Description
Warfarin maintenance dose on the basis of demographic/pharmacogenetic data
Intervention Type
Genetic
Intervention Name(s)
Calculate warfarin dose using demographic/genetic algorithm
Intervention Description
Age, body weight and genetic to calculate warfarin dosage
Primary Outcome Measure Information:
Title
International Normalized Ratio (INR)
Description
Number of INR outside the therapeutic range (INR 2.0-3.0)
Time Frame
Day 0, 5, 7, 9, 12, 15, 19.
Secondary Outcome Measure Information:
Title
Number of changes in warfarin dosage
Time Frame
Day 0-19
Title
Difference between predicted and actual warfarin maintenance dose
Time Frame
Day 19
Title
Thromboembolic and Bleeding complications
Time Frame
Day 0-30

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age >18 years Indication to warfarin with INR between 2.0 and 3.0 Exclusion Criteria: Pregnancy Drug interactions Basal INR > 1.2
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vittorio Pengo, M.D.
Organizational Affiliation
University of Padova
Official's Role
Principal Investigator
Facility Information:
Facility Name
Thrombosis Centre
City
Padova
ZIP/Postal Code
35128
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
26710337
Citation
Pengo V, Zambon CF, Fogar P, Padoan A, Nante G, Pelloso M, Moz S, Frigo AC, Groppa F, Bozzato D, Tiso E, Gnatta E, Denas G, Padayattil Jose S, Padrini R, Basso D, Plebani M. A Randomized Trial of Pharmacogenetic Warfarin Dosing in Naive Patients with Non-Valvular Atrial Fibrillation. PLoS One. 2015 Dec 28;10(12):e0145318. doi: 10.1371/journal.pone.0145318. eCollection 2015.
Results Reference
derived

Learn more about this trial

Early Identification of Warfarin Maintenance Dosage

We'll reach out to this number within 24 hrs