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Trimetazidine Therapy in Hypertrophic Cardiomyopathy

Primary Purpose

Hypertrophic Cardiomyopathy

Status
Unknown status
Phase
Phase 2
Locations
United Kingdom
Study Type
Interventional
Intervention
Trimetazidine
Placebo capsule
Sponsored by
University College, London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypertrophic Cardiomyopathy focused on measuring Trimetazidine

Eligibility Criteria

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

Inclusion Criteria:

  • Non-obstructive hypertrophic cardiomyopathy (gradient <30 mmHg at rest)
  • NYHA (New York Heart Association) Class ≥ 2
  • Peak VO2 (maximal oxygen consumption) ≤80% predicted for age and gender
  • Heart rate < 90/minute at rest

Exclusion Criteria:

  • Diabetes Mellitus
  • Abnormal renal function (GFR<60ml/min) or hepatic impairment
  • Female who is pregnant, lactating or planning pregnancy during the course of the study

Sites / Locations

  • The Heart Hospital, UCLHRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Trimetazidine

Placebo capsule

Arm Description

Outcomes

Primary Outcome Measures

Peak oxygen consumption

Secondary Outcome Measures

Left ventricular function
TDI and 2D strain
Symptom status
questionnaire
Arrhythmia
24 Hour Holter
Cardiac biomarkers
Exercise capacity
6 minute walk test

Full Information

First Posted
September 27, 2012
Last Updated
February 27, 2013
Sponsor
University College, London
Collaborators
British Heart Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT01696370
Brief Title
Trimetazidine Therapy in Hypertrophic Cardiomyopathy
Official Title
A Phase 2b Randomised, Double Blind, Placebo-controlled Trial of Trimetazidine Therapy in Patients With Non-obstructive Hypertrophic Cardiomyopathy
Study Type
Interventional

2. Study Status

Record Verification Date
August 2011
Overall Recruitment Status
Unknown status
Study Start Date
April 2012 (undefined)
Primary Completion Date
April 2014 (Anticipated)
Study Completion Date
April 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University College, London
Collaborators
British Heart Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Hypertrophic cardiomyopathy (HCM) is a common inherited heart condition that causes breathlessness, chest pain and fatigue. There are few treatments available. The investigators have recently shown that a drug called perhexiline reduced symptoms and improved exercise capacity in patients with HCM. This change appears to be driven by alterations in myocardial energy metabolism. The aim of this trial is to test a similar drug, trimetazidine, in a group of symptomatic patients with non-obstructive HCM. HYPOTHESIS: trimetazidine will improve symptoms, peak oxygen consumption, cardiac function and arrhythmia burden in medically refractory symptomatic patients with non-obstructive HCM.
Detailed Description
BACKGROUND: Hypertrophic cardiomyopathy (HCM) is a common inherited disorder of heart muscle affecting 1 in 500 individuals worldwide. It is associated with arrhythmias, heart failure and sudden death in young people. In the majority of patients, HCM is caused by mutations in genes encoding cardiac contractile proteins. It has been hypothesised that excessive sarcomeric energy consumption is an important and early factor in the pathophysiology of HCM. Therefore modulation of myocardial metabolism presents a novel target for improving myocardial performance and symptoms in patients with HCM. Trimetazidine is an anti-anginal agent which like perhexiline reduces fatty acid oxidation and increases glucose oxidation, thus increasing the efficiency of energy production. Trimetazidine has been shown to significantly improve exercise performance in patients with stable angina, ischaemic and non ischaemic cardiomyopathy, either as monotherapy or in combination with beta-blockers or calcium channel blockers, DESIGN: A single centre prospective randomised, double blind, placebo-controlled, trial of trimetazidine therapy. DOSING: 20 mg Trimetazidine or Placebo three times daily for three months METHODS: The following assessments will be made at baseline and after 3 months treatment: history and physical examination, Minnesota heart failure questionnaire, fasting blood tests, electrocardiogram, echocardiogram, cardiopulmonary exercise test, six minute walk test, 24 hour ECG Holter monitor.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertrophic Cardiomyopathy
Keywords
Trimetazidine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Trimetazidine
Arm Type
Active Comparator
Arm Title
Placebo capsule
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Trimetazidine
Intervention Description
Trimetazidine 20mg three times per day for 3 months
Intervention Type
Other
Intervention Name(s)
Placebo capsule
Intervention Description
one capsule three times per day for 3 months
Primary Outcome Measure Information:
Title
Peak oxygen consumption
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Left ventricular function
Description
TDI and 2D strain
Time Frame
3 months
Title
Symptom status
Description
questionnaire
Time Frame
3 months
Title
Arrhythmia
Description
24 Hour Holter
Time Frame
3 months
Title
Cardiac biomarkers
Time Frame
3 months
Title
Exercise capacity
Description
6 minute walk test
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Non-obstructive hypertrophic cardiomyopathy (gradient <30 mmHg at rest) NYHA (New York Heart Association) Class ≥ 2 Peak VO2 (maximal oxygen consumption) ≤80% predicted for age and gender Heart rate < 90/minute at rest Exclusion Criteria: Diabetes Mellitus Abnormal renal function (GFR<60ml/min) or hepatic impairment Female who is pregnant, lactating or planning pregnancy during the course of the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Perry M Elliott, MBBS MD
Phone
020 3456 7898
Email
p.elliott@ucl.ac.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Caroline J Coats, MBBS
Phone
020 3456 7898
Email
c.coats@ucl.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Perry M Elliott, MBBS MD
Organizational Affiliation
University College, London
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Heart Hospital, UCLH
City
London
ZIP/Postal Code
W1G 8PH
Country
United Kingdom
Individual Site Status
Recruiting

12. IPD Sharing Statement

Citations:
PubMed Identifier
30725091
Citation
Coats CJ, Pavlou M, Watkinson OT, Protonotarios A, Moss L, Hyland R, Rantell K, Pantazis AA, Tome M, McKenna WJ, Frenneaux MP, Omar R, Elliott PM. Effect of Trimetazidine Dihydrochloride Therapy on Exercise Capacity in Patients With Nonobstructive Hypertrophic Cardiomyopathy: A Randomized Clinical Trial. JAMA Cardiol. 2019 Mar 1;4(3):230-235. doi: 10.1001/jamacardio.2018.4847.
Results Reference
derived

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Trimetazidine Therapy in Hypertrophic Cardiomyopathy

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