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Assessment of the Relations Between Endothelial and Venous Dysfunctions and Left Ventricular Obstruction in Genetic Hypertrophic Cardiomyopathies (HCM-Vein)

Primary Purpose

Hypertrophic Cardiomyopathy, Endothelial Dysfunction

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
BNP blood sample test
Electrocardiogram
Holter ECG
Echocardiography
Air venous plethysmography
Upper member arterial Doppler echography with analysis of FMD
Endothelial function biomarkers
Sponsored by
University Hospital, Bordeaux
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Hypertrophic Cardiomyopathy focused on measuring Hypertrophic Cardiomyopathy, Endothelial Dysfunction, Venous return, Left ventricular outflow-tract obstruction, Sudden cardiac death risk

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients and volunteers:

    • Adults (age ≥18 years), male or female,
    • For female in age, efficient contraception will be required and a negative pregnancy test will be required,
    • Signed informed consent form will required for each included subject after having read the information note,
    • Affiliated to the national social security system,
  • Patients:

    .Patients diagnosed to have HCM secondary to sarcomeric mutation or to Fabry disease, symptomatic (dyspnea on exertion and/or chest pains during exercise),

  • Healthy volunteers:

    • Subjects without known cardiac disease,
    • No smokers.

Exclusion Criteria:

  • Patients and volunteers:

    • No cardiac pathology reducing life expectancy to less than 12 months (cancer),
    • Unbalanced arterial hypertension (systolic >160 mmHg and/or diastolic >120 mmHg),
    • Pregnancy or breastfeeding,
    • Major obesity > 140 kg,
    • Impossibility or refusal to give or sign the consent form,
    • Subject in period of exclusion relative to an other protocol,
    • Subject deprived of liberty by judicial or administrative decision,
    • Major protected by the Law
  • Patients:

    • Atrial fibrillation at the time of inclusion
    • Valvulopathy with severity greater than moderate.

Sites / Locations

  • University Hospital, Bordeaux

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Symptomatic HCM patients

Healthy controls subjects

Arm Description

30 subjects (25-26 sarcomeric, 4-5 Fabry).

10 subjects (matched in age and sex to HCM patients) to obtain reference values of endothelial dysfunction.

Outcomes

Primary Outcome Measures

Assessment of the venous ejection fraction
Via a plethysmography exam. The venous ejection fraction is measured in percentage.
Assessment of the caliber variation of the brachial artery
Via a recording of arterial Doppler echography with analysis of FMD parameters. This parameter is measured in percentage.
Measure of the Willebrand factor
The analysis of this biomarker of endothelial function is performed via a peripheral venous sample. This biomarker is measured in percentage.

Secondary Outcome Measures

Full Information

First Posted
June 12, 2019
Last Updated
February 21, 2022
Sponsor
University Hospital, Bordeaux
Collaborators
Fédération Française de Cardiologie, Fondation Bordeaux Université, Amicus Therapeutics
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1. Study Identification

Unique Protocol Identification Number
NCT04129905
Brief Title
Assessment of the Relations Between Endothelial and Venous Dysfunctions and Left Ventricular Obstruction in Genetic Hypertrophic Cardiomyopathies
Acronym
HCM-Vein
Official Title
Assessment of the Relations Between Endothelial and Venous Dysfunctions and Left Ventricular Obstruction in Genetic Hypertrophic Cardiomyopathies
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Completed
Study Start Date
October 22, 2019 (Actual)
Primary Completion Date
December 14, 2021 (Actual)
Study Completion Date
December 14, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Bordeaux
Collaborators
Fédération Française de Cardiologie, Fondation Bordeaux Université, Amicus Therapeutics

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Left ventricular obstruction is an invalidating complication of hypertrophic cardiomyopathies (HCM), and endothelial dysfunction has also been observed in these pathologies. However, the relation between obstruction and endothelial and venous dysfunctions has not been previously studied. The main objective is to investigate the relations between endothelial and venous dysfunctions and symptomatic left ventricular outflow-tract obstruction in HCM patients.
Detailed Description
Hypertrophic cardiomyopathies (HCM) secondary to sarcomeric gene mutation or to Anderson-Fabry disease can be complicated by left ventricular (LV) outflow-tract obstruction responsible of disabling exercise symptoms. LV outflow-tract obstruction is a complex, multifactorial and dynamical phenomenon influenced by the degree of LV hypertrophy but also by mitral valve elongation and hemodynamical components including venous return (LV preload). The clinical and research team of Dr Réant, responsible of the Bordeaux Competence Center in hereditary or rare Cardiomyopathies, has recently demonstrated that LV outflow-tract obstruction can also be influenced by the conditions of realization of exercise echocardiography tests (position: upright versus supine, type: bicycle versus treadmill), and by an abnormal venous return capacity. In parallel, it has also been demonstrated, by other research teams, that HCM can be associated to endothelial and microvascular peripheral dysfunctions. However, to date, the relation between these two elements, and with sudden cardiac death risk, have not been previously studied. The tests which will be performed during normal recommended follow-up of the HCM patients will be: Brain Natriuretic Peptide (BNP) blood sample test, electrocardiogram (ECG), Holter ECG, echocardiography at rest and during exercise. The tests realized in addition will be: air venous plethysmography: non invasive, and non painful test evaluating different parameters of venous filling by inflation of an armband around the leg, upright positioning, flexion-extension of the leg. Total duration estimated at 30-45 minutes. upper member arterial Doppler echography with analysis of Flow Mediated Dilatation (FMD) : measurement of the evolution of brachial artery diameter before and after inflation of a armband during 5 minutes. Non invasive and non painful test, duration 30 minutes.. endothelial function biomarkers: blood sample test, 5 minutes. No follow-up is required for this study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertrophic Cardiomyopathy, Endothelial Dysfunction
Keywords
Hypertrophic Cardiomyopathy, Endothelial Dysfunction, Venous return, Left ventricular outflow-tract obstruction, Sudden cardiac death risk

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Symptomatic HCM patients
Arm Type
Experimental
Arm Description
30 subjects (25-26 sarcomeric, 4-5 Fabry).
Arm Title
Healthy controls subjects
Arm Type
Active Comparator
Arm Description
10 subjects (matched in age and sex to HCM patients) to obtain reference values of endothelial dysfunction.
Intervention Type
Biological
Intervention Name(s)
BNP blood sample test
Intervention Description
Performed during normal recommended follow-up of the HCM patients.
Intervention Type
Diagnostic Test
Intervention Name(s)
Electrocardiogram
Intervention Description
Performed during normal recommended follow-up of the HCM patients.
Intervention Type
Diagnostic Test
Intervention Name(s)
Holter ECG
Intervention Description
Performed during normal recommended follow-up of the HCM patients.
Intervention Type
Diagnostic Test
Intervention Name(s)
Echocardiography
Intervention Description
Performed during normal recommended follow-up of the HCM patients. Echocardiography at rest and during exercise.
Intervention Type
Diagnostic Test
Intervention Name(s)
Air venous plethysmography
Intervention Description
Performed specifically for the research. Non invasive, and non painful test evaluating different parameters of venous filling by inflation of an armband around the leg, upright positioning, flexion-extension of the leg. Total duration estimated at 30-45 minute.
Intervention Type
Diagnostic Test
Intervention Name(s)
Upper member arterial Doppler echography with analysis of FMD
Intervention Description
Performed specifically for the research. Measurement of the evolution of brachial artery diameter before and after inflation of a armband during 5 minutes. Non invasive and non painful test, duration 30 minutes.
Intervention Type
Biological
Intervention Name(s)
Endothelial function biomarkers
Intervention Description
Performed specifically for the research. Blood sample test, 5 minutes.
Primary Outcome Measure Information:
Title
Assessment of the venous ejection fraction
Description
Via a plethysmography exam. The venous ejection fraction is measured in percentage.
Time Frame
Day 0
Title
Assessment of the caliber variation of the brachial artery
Description
Via a recording of arterial Doppler echography with analysis of FMD parameters. This parameter is measured in percentage.
Time Frame
Day 0
Title
Measure of the Willebrand factor
Description
The analysis of this biomarker of endothelial function is performed via a peripheral venous sample. This biomarker is measured in percentage.
Time Frame
Day 0

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients and volunteers: Adults (age ≥18 years), male or female, For female in age, efficient contraception will be required and a negative pregnancy test will be required, Signed informed consent form will required for each included subject after having read the information note, Affiliated to the national social security system, Patients: .Patients diagnosed to have HCM secondary to sarcomeric mutation or to Fabry disease, symptomatic (dyspnea on exertion and/or chest pains during exercise), Healthy volunteers: Subjects without known cardiac disease, No smokers. Exclusion Criteria: Patients and volunteers: No cardiac pathology reducing life expectancy to less than 12 months (cancer), Unbalanced arterial hypertension (systolic >160 mmHg and/or diastolic >120 mmHg), Pregnancy or breastfeeding, Major obesity > 140 kg, Impossibility or refusal to give or sign the consent form, Subject in period of exclusion relative to an other protocol, Subject deprived of liberty by judicial or administrative decision, Major protected by the Law Patients: Atrial fibrillation at the time of inclusion Valvulopathy with severity greater than moderate.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patricia REANT, MD
Organizational Affiliation
University Hospital, Bordeaux
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital, Bordeaux
City
Pessac
ZIP/Postal Code
33604
Country
France

12. IPD Sharing Statement

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Assessment of the Relations Between Endothelial and Venous Dysfunctions and Left Ventricular Obstruction in Genetic Hypertrophic Cardiomyopathies

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