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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00854698
Other study ID # 4199
Secondary ID 2008-A00663-52
Status Completed
Phase N/A
First received March 2, 2009
Last updated June 20, 2014
Start date June 2009
Est. completion date April 2014

Study information

Verified date June 2014
Source University Hospital, Strasbourg, France
Contact n/a
Is FDA regulated No
Health authority France: Ministry of Health
Study type Interventional

Clinical Trial Summary

The real impact of the existence of an aortic valve mismatch after aortic valve replacement in various studies conducted so far is a source of controversy. There is currently no long-term impact of the aortic valve mismatch on the reversal of left ventricular remodeling and its impact functional.To evaluate these effects of aortic valve mismatch on abilities to the effort, the quality of life and the regression of left ventricular hypertrophy long term after a aortic valve replacement, conducting a new study is fundamental. This study is even more essential in patients with a young life expectancy theoretical long and physical activity.Our study aims to determine whether the existence of an aortic valve mismatch has an influence on: The functional capacity to the effort by measuring the maximum oxygen consumption during a stress test (VO2 max) The reversal of left ventricular remodeling (cardiac ultrasound doppler), diastolic dysfunction (cardiac ultrasound and Doppler measurement Brain Natriuretic Peptide (BNP). This study will analyse these data in patients who received youth a VAN by mechanical aortic valve prosthesis.


Recruitment information / eligibility

Status Completed
Enrollment 77
Est. completion date April 2014
Est. primary completion date April 2014
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Patient major = 60 years at the time of the aortic valve replacement.

- Patient affiliated with a social security

- Consent dated and signed by the investigator and the subject

- Subject having been informed of the results of the visit prior aortic valve replacement by mechanical prosthesis for pure aortic narrowing.

- Fraction left ventricular ejection = 50%, when aortic valve replacement and at the time of inclusion.

- Aortic insufficiency at aortic valve replacement associated <II / IV.

- aortic valve replacement exclusive (no gestures associated: coronary bypass, enlargement of the ring, another valve surgery,…).

- Coronarography normal at the aortic valve replacement.

- Normal renal function.

- No history of heart failure episode in the previous month inclusion.

- No indication against a stress test on bicycle ergometric

Exclusion Criteria:

- Refusal of the patient to be included in the study.

- History of cardiac surgery under extra body movement before and / or after the aortic valve replacement.

- Aortic insufficiency associated with the time of the transaction> II / IV.

- Chronic respiratory insufficiency.

- Track cancer or cancer evolving.

- Evolutionary Osteoarthritis of the lower limbs or widespread.

- Myopathy device.

- Alteration higher making it impossible to carry out the test effort and response to the questionnaire on the quality of life.

- Coronaropathy documented.

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Other:
exercise training
subjects are asked to exercise 20 or 30 minutes.
subjects are asked to exercise during 20 or 30 minutes
subjects are asked to exercise during 20 or 30 minutes

Locations

Country Name City State
France CHRU, Nouvel Hôpital Civil, Service de chirurgie cardio-vasculaire Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary variations in VO2 max during an effort 1 year No
Secondary Study the impact of a MVA after RVA by mechanical prosthesis 1 year No