Characterization of Myocardial Interstitial Fibrosis and Cardiomyocyte Hypertrophy by Cardiac MRI in Heart Failure
2 other identifiers
interventional
90
1 country
1
Brief Summary
The investigators hypothesised that novel MRI metrics derived from myocardium post-gadolinium T1 mapping analysis will improve the current knowledge about the role interstitial fibrosis and cardiomyocyte hypertrophy in the development of left ventricular (LV) remodelling and clinical Heart Failure (HF). The investigators believe that these recently described variables will be associated with prognostically important indices in HF development.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable heart-failure
Started Nov 2017
Typical duration for not_applicable heart-failure
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 25, 2016
CompletedFirst Posted
Study publicly available on registry
March 21, 2017
CompletedStudy Start
First participant enrolled
November 1, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2020
CompletedJune 5, 2019
June 1, 2019
1.6 years
December 25, 2016
June 3, 2019
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Myocardial remodeling assessed by CMR in rehabilitation vs usual care.
Investigate whether rehabilitation compared to usual care is associated with significant favorable myocardial remodeling assessed by CMR determination of ECV.
4 months
Secondary Outcomes (17)
Change in left ventricular ejection fraction
4 months
Change in right ventricular ejection fraction
4 months
Change in left ventricular mass (absolute/index)
4 months
Change in left ventricular diastolic volume (absolute/index)
4 months
Change in right ventricular diastolic volume (absolute/index)
4 months
- +12 more secondary outcomes
Study Arms (4)
Conventional Clinical Care - HFpEF
NO INTERVENTIONHeart Failure patients with preserved ejection fraction (HFpEF) randomized to this arm will keep receiving their conventional clinical care, being instructed to continue and maintain their usual daily activities.
Supervised Exercise Training- HFpEF
OTHERHeart Failure patients with preserved ejection fraction (HFpEF) randomized to this arm will keep receiving their conventional clinical care and participate in a supervised, facility based training program consisting of stretching exercises and aerobic exercise in treadmill.
Conventional Clinical Care - HFrEF
NO INTERVENTIONHeart Failure patients with reduced ejection fraction (HFrEF) randomized to this arm will keep receiving their conventional clinical care, being instructed to continue and maintain their usual daily activities.
Supervised Exercise Training - HFrEF
OTHERHeart Failure patients with reduced ejection fraction (HFrEF) randomized to this arm will keep receiving their conventional clinical care and participate in a supervised, facility based training program consisting of stretching exercises and aerobic exercise in treadmill.
Interventions
30-40min of aerobic exercise in treadmill. The aerobic intensity will be established by heart rate levels that corresponded to anaerobic threshold up to 10% below the respiratory compensation point obtained in the cardiopulmonary exercise test. This intensity corresponded to 60-72% peak V̀‡o2. During the exercise sessions, when a training effect will be observed, as indicated by a decrease by 8 to 10% in heart rate, the treadmill velocity or inclination will be increased to return to the target heart rate levels.
15 min of local strengthening exercises will be performed in major muscle groups (legs, arms and trunk muscles): three series of each exercise, 12-15 repetitions.
5-min stretching exercises will be performed in major muscle groups (legs, arms and trunk muscles)
Eligibility Criteria
You may qualify if:
- Age\> 18 years
- Functional limitation (New York Heart Association Class II or worse)
- No contraindication to exercise (American College of Cardiology / American Heart Association criteria)
- Eligibility to take MRI (absence of metallic devices, and glomerular filtration rate \> 40ml / min / 1.73m2, etc.)
- Prior diagnosis of Heart Failure (by the Framingham criterion)
- Therapy with diuretic and euvolemia state (evaluated by cardiologist and cardiopulmonary exercise testing)
- Transthoracic echocardiogram
You may not qualify if:
- Severe ischemia in any stress test
- Hypertrophic cardiomyopathy or any infiltrative heart disease
- Chronic obstructive pulmonary disease , pulmonary hypertension (Pulmonary artery pressure\> 60mmHg)
- Severe left or right valve disease.
- Pacemaker or implantable cardioverter defibrillator
- Myocardial infarction or revascularization in 3 months
- Anemia (hemoglobin \<10 grams / dl) until 1 month before cardiopulmonary exercise testing
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Campinas
Campinas, SĂ£o Paulo, Brazil
Related Publications (44)
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PMID: 19091900BACKGROUND
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
OTAVIO R COELHO-FILHO, MD, MPH, PhD
University of Campinas, Brazil
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
December 25, 2016
First Posted
March 21, 2017
Study Start
November 1, 2017
Primary Completion
June 1, 2019
Study Completion
July 1, 2020
Last Updated
June 5, 2019
Record last verified: 2019-06
Data Sharing
- IPD Sharing
- Will not share
No plan to Share individual participant data.