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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02579954
Other study ID # 1308156
Secondary ID 2014-A00169-38
Status Recruiting
Phase N/A
First received
Last updated
Start date August 6, 2015
Est. completion date June 2024

Study information

Verified date March 2024
Source Centre Hospitalier Universitaire de Saint Etienne
Contact Laurent BERTOLETTI, MD PhD
Phone 0477127770
Email laurent.bertoletti@chu-st-etienne.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Pulmonary Arterial Hypertension is characterized by a progressive increase in pulmonary vascular resistance inducing shortness of breath and exercise intolerance. We aim to correlate cardiac function (evaluated at rest by right heart catheterism and RMN) to exercise capacity (evaluated by endurance time at 75% of maximal workout), in prevalent patients with pulmonary arterial hypertension, and their evolution at three and twelve months.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date June 2024
Est. primary completion date June 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult patients - Patients with Pulmonary Arterial Hypertension (idiopathic, heritable or due to anorexigens), - Prevalent cases of pulmonary artery hypertension (= 6 months) confirmed by right heart catheterism, - Stable for at least 3 months, - Written consent. Exclusion Criteria: - Patients unable to proceed with six-minute walk test or CPET, or with contra-indication to exercise evaluation (syncope, low cardiac index, etc). - Exercise induced abnormality (evaluated during the initial CPET) precluding to further evaluation.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Rehabilitation


Locations

Country Name City State
France CHU de Besançon Besancon
France CHU de Brest Brest
France CHU Gabriel Montpied Clermont Ferrand
France Hôpital Sud de Grenoble Echirolles
France Hôpital Nord de Grenoble Grenoble
France HCL - Hôpital Louis Pradel Lyon
France CHU de Montpellier Montpellier
France APHP - Hôpital Bicêtre Paris
France Chu de Saint Etienne Saint Etienne
France CHRU de Strasbourg Strasbourg

Sponsors (2)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire de Saint Etienne Ministry of Health, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Endurance time at 75% of the maximal workout (determinated during a cardiopulmonary exercise testing - CPET), 12 months after the inclusion
Secondary Right ventricular ejection fraction evaluated by RMN at 3 and 12 months
Secondary Pulmonary haemodynamics : measurements at right heart catheterism cardiac index (L/min/m²) at 3 and 12 months
Secondary Pulmonary haemodynamics : measurements at right heart catheterism pressure in the right atrium (mmHg) at 3 and 12 months
Secondary Pulmonary haemodynamics : measurements at right heart catheterism pulmonary resistance (uw) at 3 and 12 months
Secondary Pulmonary haemodynamics : measurements at right heart catheterism mean pulmonary arterial pressure (mmHg) at 3 and 12 months
Secondary Functional class (NYHA classification) at 3 and 12 months
Secondary 6 minutes walking distance (m) at 3 and 12 months
Secondary Functional exercise capacity (oxygen consumption measurement during test) at 3 and 12 months
Secondary Quality of life (SF-36 scale) at 3 and 12 months
Secondary Time to clinical worsening (months) at 3 and 12 months
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