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Low INR to Minimize Bleeding With Mechanical Valves Trial (LIMIT)

Primary Purpose

Bleeding Post-mechanical Valve Replacement, Thromboembolism Post-mechanical Valve Replacement

Status
Recruiting
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
Warfarin
Sponsored by
Population Health Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bleeding Post-mechanical Valve Replacement focused on measuring Mechanical valve replacement, Vitamin K antagonist, INR targets, Bleeding, Thromboembolism

Eligibility Criteria

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

Inclusion criteria:

  • Age is 18 or older at the time of enrolment
  • Have had a bileaflet mechanical heart valve implant in the aortic position 3 or more months ago
  • Written informed consent from either the patient or substitute decision maker

Exclusion criteria:

  • Has a second implanted mechanical valve (any position)
  • Lower boundary of planned INR range is less than 2.0
  • Pregnant or expecting to become pregnant during the study follow-up
  • On-X Valve

Sites / Locations

  • Universitair Ziekenhuis LeuvenRecruiting
  • Hamilton General HospitalRecruiting
  • Jewish General HospitalRecruiting
  • Erasmus University Medical CentreRecruiting
  • Meshalkin National Medical Research CenterRecruiting
  • Hospital de la Santa Creu i Sant PauRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Reduced INR Target

Standard INR Target

Arm Description

Warfarin therapy will be titrated to a target INR in the range of 1.5 to 2.5.

Warfarin therapy will be titrated to a "standard of care" target INR range.

Outcomes

Primary Outcome Measures

Thrombosis/thromboembolism
Number of patients who have at least one of the following: ischemic stroke, systemic thromboembolism, and valve thrombosis
Major bleeding
Number of patients that have bleeding that results in the following: Death and/or, Symptomatic bleeding in critical area or organ (e.g. intracranial, intraspinal, intraocular, retroperitoneal, intraarticular, pericardial, or intramuscular with compartment syndrome) and/or, Bleeding that causes drop of hemoglobin level by 20 g/L or more, or that requires the transfusion of 2 or more units of packed red blood cells or whole blood

Secondary Outcome Measures

All cause mortality
Selected rather than cardiovascular mortality, as cause-specific mortality is often difficult to ascertain or define in complex cardiovascular patients in whom multi-end-organ dysfunction may accompany cardiovascular decline.
All clinically important bleeding
Number of patients that experience all clinically important bleeding (major and minor)
Minor bleeding
Number of patients that experience a bleed that does not meet major bleeding criteria and leads to at least one of: Hospital admission Requires medical or surgical management Requires interruption or discontinuation of study drug
All stroke
Number of patients that experience a strokes, including ischemic stroke, ischemic with secondary transformation, stroke of uncertain classification and hemorrhagic stroke
Ischemic stroke
Number of patients that experience an ischemic stroke, defined as focal brain infarction caused by an arterial (or rarely venous) obstruction and as documented by CT/MRI that is normal or shows an infarct in the clinicall expected area
Hemorrhagic stroke
Number of patients that experience a hemorrhagic stroke, defined as requiring neuroimaging or autopsy confirmation, and includes two subcategories: primary intracerebral hemorrhage and primary subarachnoid hemorrhage
Type 1, 2 or 3 myocardial infarction
Number of patients who experience a type 1, 2 or 3 myocardial infarction
Systemic thromboembolism
Number of patients who experience a systemic thromboembolism
Valve thrombosis
Number of patients who experience a valve thrombosis
Pulmonary embolism
Number of patients who experience a pulmonary embolism
Deep vein thrombosis
Number of patients who experience a deep vein thrombosis
New renal replacement therapy
Number of patients requiring new renal replacement therapy
Time in therapeutic range
The percentage of time the patient's INR was within the target range
Proportion of patients with extreme INR values (>4)
The proportion of patients with at least one reported INR value above 4

Full Information

First Posted
July 25, 2018
Last Updated
January 18, 2023
Sponsor
Population Health Research Institute
Collaborators
Hamilton Health Sciences Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT03636295
Brief Title
Low INR to Minimize Bleeding With Mechanical Valves Trial
Acronym
LIMIT
Official Title
Low INR to Minimize Bleeding With Mechanical Valves Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
September 5, 2019 (Actual)
Primary Completion Date
March 31, 2025 (Anticipated)
Study Completion Date
April 30, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Population Health Research Institute
Collaborators
Hamilton Health Sciences Corporation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study evaluates the use of a lower INR target (1.5 to 2.5) in patients with a mechanical bileaflet heart valve in the aortic position. This study will inform physicians about whether a lower INR target will decrease the risk of bleeding or increase the risk of blood clot formation and stroke. These results have the potential to reduce the burden of bleeding in patients with a mechanical heart valve who require lifelong warfarin (Coumadin) treatment.
Detailed Description
Warfarin (Coumadin) is a blood thinner used to prevent blood clot formation in patients with mechanical heart valves. Blood clots can block blood flow to the brain, heart, or other parts of the body. Mechanical heart valves increases the risk of clot so patients with a mechanical heart valve must take warfarin to reduce their risk of stroke and other blood clot-related problems. The degree to which warfarin 'works' varies from person to person, and so dosage is determined by measuring each person's response to the drug as an 'international normalized ratio' or INR. A patient with an INR over 1.0 has blood that takes longer to clot than average, and increasing INR values represent increasing time required for blood to clot. While an INR over 1.0 decreases clotting risk, it also increases bleeding risk. It is important to carefully balance these risks. Specific INR targets have been recommended for patients with a mechanical heart valve, but these recommendations differ between scientific groups and are based on low quality evidence. Recent studies suggest that a lower INR target range than is currently recommended can be used safely. A laboratory study showed that warfarin effectively prevents blood clot formation on mechanical heart valves as long as the INR is 1.5 or above. Two moderately-sized clinical studies showed that an INR target range of 1.5-2.5 resulted in less bleeding than the usual higher target range without increasing blood clot formation or stroke in patients with a newer valve model. Whether we could use a lower INR target range for patients with a mechanical aortic valve remains controversial. This study evaluates the use of a lower INR target (1.5 to 2.5) in patients with a mechanical bileaflet heart valve in the aortic position. This study will inform physicians about whether a lower INR target will decrease the risk of bleeding or increase the risk of blood clot formation and stroke. These results have the potential to reduce the burden of bleeding in patients with a mechanical heart valve who require lifelong warfarin (Coumadin) treatment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bleeding Post-mechanical Valve Replacement, Thromboembolism Post-mechanical Valve Replacement
Keywords
Mechanical valve replacement, Vitamin K antagonist, INR targets, Bleeding, Thromboembolism

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
A prospective, randomized, open-label, blinded end-point (PROBE) clinical trial.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
2625 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Reduced INR Target
Arm Type
Experimental
Arm Description
Warfarin therapy will be titrated to a target INR in the range of 1.5 to 2.5.
Arm Title
Standard INR Target
Arm Type
Active Comparator
Arm Description
Warfarin therapy will be titrated to a "standard of care" target INR range.
Intervention Type
Drug
Intervention Name(s)
Warfarin
Other Intervention Name(s)
Coumadin
Intervention Description
Participants in both arms will be on warfarin therapy post-mechanical valve replacement as is standard, but will have different INR target ranges.
Primary Outcome Measure Information:
Title
Thrombosis/thromboembolism
Description
Number of patients who have at least one of the following: ischemic stroke, systemic thromboembolism, and valve thrombosis
Time Frame
Through study completion, an expected mean of 2-3 years
Title
Major bleeding
Description
Number of patients that have bleeding that results in the following: Death and/or, Symptomatic bleeding in critical area or organ (e.g. intracranial, intraspinal, intraocular, retroperitoneal, intraarticular, pericardial, or intramuscular with compartment syndrome) and/or, Bleeding that causes drop of hemoglobin level by 20 g/L or more, or that requires the transfusion of 2 or more units of packed red blood cells or whole blood
Time Frame
Through study completion, an expected mean of 2-3 years
Secondary Outcome Measure Information:
Title
All cause mortality
Description
Selected rather than cardiovascular mortality, as cause-specific mortality is often difficult to ascertain or define in complex cardiovascular patients in whom multi-end-organ dysfunction may accompany cardiovascular decline.
Time Frame
Through study completion, an expected mean of 2-3 years
Title
All clinically important bleeding
Description
Number of patients that experience all clinically important bleeding (major and minor)
Time Frame
Through study completion, an expected mean of 2-3 years
Title
Minor bleeding
Description
Number of patients that experience a bleed that does not meet major bleeding criteria and leads to at least one of: Hospital admission Requires medical or surgical management Requires interruption or discontinuation of study drug
Time Frame
Through study completion, an expected mean of 2-3 years
Title
All stroke
Description
Number of patients that experience a strokes, including ischemic stroke, ischemic with secondary transformation, stroke of uncertain classification and hemorrhagic stroke
Time Frame
Through study completion, an expected mean of 2-3 years
Title
Ischemic stroke
Description
Number of patients that experience an ischemic stroke, defined as focal brain infarction caused by an arterial (or rarely venous) obstruction and as documented by CT/MRI that is normal or shows an infarct in the clinicall expected area
Time Frame
Through study completion, an expected mean of 2-3 years
Title
Hemorrhagic stroke
Description
Number of patients that experience a hemorrhagic stroke, defined as requiring neuroimaging or autopsy confirmation, and includes two subcategories: primary intracerebral hemorrhage and primary subarachnoid hemorrhage
Time Frame
Through study completion, an expected mean of 2-3 years
Title
Type 1, 2 or 3 myocardial infarction
Description
Number of patients who experience a type 1, 2 or 3 myocardial infarction
Time Frame
Through study completion, an expected mean of 2-3 years
Title
Systemic thromboembolism
Description
Number of patients who experience a systemic thromboembolism
Time Frame
Through study completion, an expected mean of 2-3 years
Title
Valve thrombosis
Description
Number of patients who experience a valve thrombosis
Time Frame
Through study completion, an expected mean of 2-3 years
Title
Pulmonary embolism
Description
Number of patients who experience a pulmonary embolism
Time Frame
Through study completion, an expected mean of 2-3 years
Title
Deep vein thrombosis
Description
Number of patients who experience a deep vein thrombosis
Time Frame
Through study completion, an expected mean of 2-3 years
Title
New renal replacement therapy
Description
Number of patients requiring new renal replacement therapy
Time Frame
Through study completion, an expected mean of 2-3 years
Title
Time in therapeutic range
Description
The percentage of time the patient's INR was within the target range
Time Frame
Through study completion, an expected mean of 2-3 years
Title
Proportion of patients with extreme INR values (>4)
Description
The proportion of patients with at least one reported INR value above 4
Time Frame
Through study completion, an expected mean of 2-3 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria: Age is 18 or older at the time of enrolment Have had a bileaflet mechanical heart valve implant in the aortic position 3 or more months ago Written informed consent from either the patient or substitute decision maker Exclusion criteria: Has a second implanted mechanical valve (any position) Lower boundary of planned INR range is less than 2.0 Pregnant or expecting to become pregnant during the study follow-up On-X Valve
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Emilie Belley-Côté, MD, MSc
Phone
905-527-4322
Ext
40306
Email
emilie.belley-cote@phri.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Richard Whitlock, MD, PhD
Phone
905-527-4322
Ext
40306
Email
richard.whitlock@phri.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emilie Belley-Côté, MD, MSc
Organizational Affiliation
McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Universitair Ziekenhuis Leuven
City
Leuven
ZIP/Postal Code
3000
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Filip Rega, MD
Facility Name
Hamilton General Hospital
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8L 2X2
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Emilie Belley-Cote, MD
Phone
905-527-4322
Ext
40306
Email
emilie.belley-cote@phri.ca
Facility Name
Jewish General Hospital
City
Montréal
State/Province
Quebec
ZIP/Postal Code
H3T 1E2
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mark Blostein, MD
Facility Name
Erasmus University Medical Centre
City
Rotterdam
ZIP/Postal Code
3015
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jolien Roos-Hesselink, MD
Facility Name
Meshalkin National Medical Research Center
City
Novosibirsk
Country
Russian Federation
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alexander Bogachev-Prokophiev, MD
Facility Name
Hospital de la Santa Creu i Sant Pau
City
Barcelona
ZIP/Postal Code
08025
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ekaterine Popova, MD
First Name & Middle Initial & Last Name & Degree
Juan Carles Souto Andres, MD

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
We will establish a plan for the full-scale study but there is no plan to make IPD available to other researchers.
Citations:
PubMed Identifier
24512654
Citation
Puskas J, Gerdisch M, Nichols D, Quinn R, Anderson C, Rhenman B, Fermin L, McGrath M, Kong B, Hughes C, Sethi G, Wait M, Martin T, Graeve A; PROACT Investigators. Reduced anticoagulation after mechanical aortic valve replacement: interim results from the prospective randomized on-X valve anticoagulation clinical trial randomized Food and Drug Administration investigational device exemption trial. J Thorac Cardiovasc Surg. 2014 Apr;147(4):1202-1210; discussion 1210-1. doi: 10.1016/j.jtcvs.2014.01.004. Epub 2014 Jan 12.
Results Reference
background
PubMed Identifier
20598989
Citation
Torella M, Torella D, Chiodini P, Franciulli M, Romano G, De Santo L, De Feo M, Amarelli C, Sasso FC, Salvatore T, Ellison GM, Indolfi C, Cotrufo M, Nappi G. LOWERing the INtensity of oral anticoaGulant Therapy in patients with bileaflet mechanical aortic valve replacement: results from the "LOWERING-IT" Trial. Am Heart J. 2010 Jul;160(1):171-8. doi: 10.1016/j.ahj.2010.05.005.
Results Reference
background

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Low INR to Minimize Bleeding With Mechanical Valves Trial

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