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REVADE : Right Ventricular Function and Exercise in Left Ventricular Assist Device Patients : Echocardiographic Study

R

Rennes University Hospital

Status

Completed

Conditions

Left Ventricular Assist Devices Patients

Treatments

Other: adding 2 cardiopulmonary exercise testings : peak oxygen consumption (VO2 max) and stress echocardiography

Study type

Interventional

Funder types

Other

Identifiers

NCT02067455
2013-A01798-37
35RC13_8808_REVADE (Other Identifier)

Details and patient eligibility

About

Heart failure is a public health problem, responsible for 150.000 admissions, 32.000 deaths, 1% of public health expenditure each year in France. Heart transplantation remains the standard of care in patients for which medical therapy is not sufficient. But heart transplantation is a limited resource, as a result of donor shortages. It is therefore possible to consider mechanical circulatory support for patients awaiting heart transplantation or for those who are not suitable for transplantation. Left Ventricular Assist Devices (LVAD) are portable pumps which help the left side of the heart to provide appropriate "cardiac" output. in this type of device, right heart is not assisted and must work on its own, LVADs are thus implanted in patients whose right ventricular function is normal.

The aim of the REVADE study is to assess right ventricular echocardiographic parameters in this population, especially on physical exercise, for a better understanding of right ventricular adaptation to this long-term modified pressure pattern.

Full description

This is a non-randomized, single-center, prospective investigation on exercise capacities of LVAD recipients.

LVAD patients already have in our unit the following regular monitoring:

  • clinical examination
  • Minnesota Living with Heart Failure Questionnaire (MLHFQ)
  • SF-36 Health Survey
  • Six-Minute Walk Test
  • resting echocardiography
  • routine blood tests.

The REVADE pilot study consists in adding 2 cardiopulmonary exercise testings to their existing follow-up : peak oxygen consumption (VO2 max) and stress echocardiography.

We plan to do 1 stress echocardiography on a supine bicycle over the follow-up, and 1 peak oxygen consumption recorded while breathing through a gas analyzer.

Total study length of time will be 1 year. Expected number of enrolled patients is 18.

Enrollment

12 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • left ventricular assist device (LVAD) recipients
  • age > 18 years
  • able to give consent

Exclusion criteria

  • adults legally protected (under judicial protection, guardianship, or supervision) or deprived of liberty
  • patients unable to provide sufficient effort for exercise testing
  • poor echogenicity

Trial design

12 participants in 1 patient group

LVAD patients
Other group
Treatment:
Other: adding 2 cardiopulmonary exercise testings : peak oxygen consumption (VO2 max) and stress echocardiography

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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