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Completed

NCT Number: NCT04129905

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital, Bordeaux

Pessac, 33604, France

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

BNP blood sample test

Biological

Performed during normal recommended follow-up of the HCM patients.

Electrocardiogram

Diagnostic Test

Performed during normal recommended follow-up of the HCM patients.

Holter ECG

Diagnostic Test

Performed during normal recommended follow-up of the HCM patients.

Echocardiography

Diagnostic Test

Performed during normal recommended follow-up of the HCM patients. Echocardiography at rest and during exercise.

Air venous plethysmography

Diagnostic Test

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.

Upper member arterial Doppler echography with analysis of FMD

Diagnostic Test

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.

Endothelial function biomarkers

Biological

Performed specifically for the research. Blood sample test, 5 minutes.

Primary outcomes

  1. Assessment of the venous ejection fraction

    Time frame: Day 0

    Via a plethysmography exam. The venous ejection fraction is measured in percentage.

  2. Assessment of the caliber variation of the brachial artery

    Time frame: Day 0

    Via a recording of arterial Doppler echography with analysis of FMD parameters. This parameter is measured in percentage.

  3. Measure of the Willebrand factor

    Time frame: Day 0

    The analysis of this biomarker of endothelial function is performed via a peripheral venous sample.

    This biomarker is measured in percentage.

Sponsors and collaborators

Lead sponsor

University Hospital, Bordeaux

Other

Collaborators

  • Amicus Therapeutics
  • Fondation Bordeaux Université
  • Fédération Française de Cardiologie

Registry information

Acronym: HCM-Vein

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Oct 17, 2019
Registry last updated
Jun 1, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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