Pulmonary Hypertension in Lymphangioleiomyomatosis (LAM-PH)

Groupe d'Etudes et de Recherche sur les Maladies Orphelines Pulmonaires

Status: Completed

Conditions: Lymphangioleiomyomatosis; Pulmonary Hypertension

Study type: Observational

Funder types: Other

Identifiers

NCT00960895

GERMOP-001

Details and patient eligibility

About

This is a descriptive study of patients with Lymphangioleiomyomatosis and precapillary pulmonary hypertension.

Full description

Descriptive study of patients with Lymphangioleiomyomatosis and precapillary pulmonary hypertension This will include modality of diagnosis of lLymphangioleiomyomatosis, results of right-sided heart catheterization, and pulmonary function tests

Enrollment: 20 patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Lymphangioleiomyomatosis (definite or probable), either sporadic or associated with tuberous sclerosis
• Precapillary pulmonary hypertension, as defined by right-sided heart catheterization (mean pulmonary artery pressure higher than 25 mmHg, wedge capillary pulmonary pressure less than 15 mmHg, pulmonary vascular resistance higher than 3 Wood units)

Exclusion criteria

• Post capillary pulmonary hypertension
• Other identifiable causes of pulmonary hypertension (ex: thromboembolic disease)
• Not willing to participate