Model-based Versus Traditional Warfarin Dosing in Children (WATCH)
Primary Purpose
Congenital Heart Defects
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Warfarin Dosing Aid
Standard Practice
Sponsored by
About this trial
This is an interventional supportive care trial for Congenital Heart Defects
Eligibility Criteria
Inclusion Criteria: -Children from birth up to 18 years with congenital heart disease who have been treated or to be treated with warfarin after undergoing reconstructive heart surgery at Glenfield Hospital, Leicester, United Kingdom.
Exclusion Criteria:
- Patients aged over 18 years who are treated as 'adults'.
- Children who refuse assent, parents who refuse consent.
- Any significant disease or disorder which, in the opinion of the direct care team, may either put the participant at risk because of study participation or adversely affect the participants' ability to participate in the study.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Warfarin dosing aid
Standard practice
Arm Description
A pharmacokinetic/pharmacodynamic model-based dosing algorithm for warfarin.
Dosing adjustments according to the normal unit protocol
Outcomes
Primary Outcome Measures
The difference between the model based and traditional warfarin dosing method in International Normalised Ratio (INR) response.
INR response includes: Time taken (days per patient) to achieve stable anticoagulation within the desired therapeutic range (TR), number and percentage of INR measurements within the TR, Time in TR, and frequency of INR measurements (number of INR measurements per month) per patient.
Secondary Outcome Measures
Medical staff perceptions of value of warfarin dosing aid
Interviews with medical staff will be conducted
Patients or carers 'lived experience' of monitoring warfarin dosing and INR
Interviews will be conducted with patients and or carers
The incidence of warfarin-related adverse events, bleeding and bruising, by recording on symptom diary cards
Full Information
NCT ID
NCT02475863
First Posted
June 12, 2015
Last Updated
June 19, 2015
Sponsor
De Montfort University
Collaborators
University Hospitals, Leicester
1. Study Identification
Unique Protocol Identification Number
NCT02475863
Brief Title
Model-based Versus Traditional Warfarin Dosing in Children
Acronym
WATCH
Official Title
A Study to Compare Model-based Warfarin Dosing to the Traditional Approach in Children After Congenital Heart Surgery at Glenfield Hospital, Leicester
Study Type
Interventional
2. Study Status
Record Verification Date
June 2015
Overall Recruitment Status
Unknown status
Study Start Date
August 2015 (undefined)
Primary Completion Date
August 2016 (Anticipated)
Study Completion Date
January 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
De Montfort University
Collaborators
University Hospitals, Leicester
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study compares the clinical effectiveness of a new algorithm (model-based warfarin dosing) with standard practice (doctor's own judgement and intuition) designed to determine the most appropriate anticoagulant dose of warfarin in children after congenital heart surgery.
Detailed Description
Warfarin is widely used in children after heart surgery in order to prevent complications that may arise due to blood clots forming in unwanted places - for example in the brain causing a stroke. If too little warfarin is given, there is a risk that clots may form. If the dose is too high, bleeding will result.
Traditionally, the approach to dosing warfarin in children has been to select a starting dose according to standard guidelines and to then adjust the doses for each child by monitoring the INR (which measures how quickly blood clots). However, a person's make up as well as external factors, such as age, weight, diet and genetics can affect warfarin dosing and this makes controlling the dose and hence controlling the INR, more difficult. Recently however, a more sophisticated dosing model has been developed by researchers which takes into account some of these factors. The model is designed to help doctors select the best dose of warfarin for children by individualising prescriptions.
The aim of the proposed research is, therefore, to compare the model based warfarin dosing with the traditional approach to warfarin dosing in children who have undergone congenital heart surgery. The research will involve children who are started on warfarin for the first time and also children who are already receiving ongoing warfarin therapy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Congenital Heart Defects
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
45 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Warfarin dosing aid
Arm Type
Experimental
Arm Description
A pharmacokinetic/pharmacodynamic model-based dosing algorithm for warfarin.
Arm Title
Standard practice
Arm Type
Active Comparator
Arm Description
Dosing adjustments according to the normal unit protocol
Intervention Type
Device
Intervention Name(s)
Warfarin Dosing Aid
Intervention Description
A pharmacokinetic/pharmacodynamic model-based dosing algorithm for warfarin
Intervention Type
Other
Intervention Name(s)
Standard Practice
Intervention Description
Warfarin dose adjustments according to standard unit protocol
Primary Outcome Measure Information:
Title
The difference between the model based and traditional warfarin dosing method in International Normalised Ratio (INR) response.
Description
INR response includes: Time taken (days per patient) to achieve stable anticoagulation within the desired therapeutic range (TR), number and percentage of INR measurements within the TR, Time in TR, and frequency of INR measurements (number of INR measurements per month) per patient.
Time Frame
6 months for warfarin naiive patients and 12 months for patients already on warfarin therapy.
Secondary Outcome Measure Information:
Title
Medical staff perceptions of value of warfarin dosing aid
Description
Interviews with medical staff will be conducted
Time Frame
Within six months of end of period of data collection
Title
Patients or carers 'lived experience' of monitoring warfarin dosing and INR
Description
Interviews will be conducted with patients and or carers
Time Frame
Within six months of end of cross-over trial
Title
The incidence of warfarin-related adverse events, bleeding and bruising, by recording on symptom diary cards
Time Frame
6 months for warfarin naiive patients and 12 months for patients already on warfarin therapy.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Day
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: -Children from birth up to 18 years with congenital heart disease who have been treated or to be treated with warfarin after undergoing reconstructive heart surgery at Glenfield Hospital, Leicester, United Kingdom.
Exclusion Criteria:
Patients aged over 18 years who are treated as 'adults'.
Children who refuse assent, parents who refuse consent.
Any significant disease or disorder which, in the opinion of the direct care team, may either put the participant at risk because of study participation or adversely affect the participants' ability to participate in the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Hussain Mulla, PhD
Phone
0116 2563323
Email
hussain.mulla@uhl-tr.nhs.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Peter Rivers, PhD
Phone
0116 2577039
Ext
7039
Email
privers@dmu.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hussain Mulla, PhD
Organizational Affiliation
Univesity Hospitals Leicester NHS Trust
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Model-based Versus Traditional Warfarin Dosing in Children
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