DHEA prevents and reverses chronic hypoxic pulmonary hypertension in a chronic hypoxic-pulmonary hypertension model in the rat. However, no study has been performed in human. The purpose of this study is to determine if DHEA is effective in the treatment of respiratory pulmonary hypertension in adults with Chronic Obstructive Pulmonary Disease (COPD) on exercise capacity and haemodynamic variables. Patients will receive after randomisation either 25 mg/day or 200mg/day oral DHEA over a one-year period. Evaluation concerns clinical parameters, echocardiography and right catheterization after and before treatment. Primary end-point is the six-minute walk test. This is a prospective double blind, randomised, placebo controlled study which will be realized in four university hospitals in France : Bordeaux, Strasbourg, Toulouse and Limoges.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
51
DHEA : 200 mg/day hard gelatine capsule
DHEA : 25 mg/day hard gelatine capsule
University Hospital, Bordeaux
Bordeaux, France
CHU de Limoges
Limoges, France
CHU de Strasbourg
Strasbourg, France
CHU de Toulouse
Toulouse, France
Efficacy of DHEA on exercise capacity (six-minute walk test)
Time frame: inclusion and one year of treatment
Pulmonary and systemic arterial pressures (mean, systolic and diastolic)
Time frame: Inclusion and after one year of treatment
Pulmonary vascular resistances
Time frame: Inclusion and after one year of treatment
Safety / Compliance
Time frame: along one year of treatment
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