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Clinical Trials/NCT02799771
NCT02799771CompletedNot Applicable

Observational Study of Incident Patients With Pre Capillary Pulmonary Hypertension and Interstitial Lung Disease

Groupe d'Etudes et de Recherche sur les Maladies Orphelines Pulmonaires1 site in 1 country210 target enrollmentStarted: February 2013Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
210
Locations
1
Primary Endpoint
Overall survival

Study Overview

Brief Summary

HYPID-2 study is an extension of HYPID study (NCT01443598) :

HYPID-2 is also an observational and prospective study of patients with interstitial lung disease and pre capillary hypertension diagnosed by right heart sided catheterization.

It concerns only incident patients (i.e patients included within 6 months after PH diagnosis) whereas HYPID concerned prevalent and incident cases.

The primary aim is the same than HYPID : identify prognostic factors

Detailed Description

Pre capillary pulmonary hypertension (PH) may be present in patients with diffuse interstitial lung disease.

In this context, PH represents an important factor of morbidity and mortality for these patients.

As in HYPID, the main purpose of HYPID-2 is to determine predictive factors of mortality within this cohort of incident patients (i.e patients included within 6 months after PH diagnosis).

In order to reach that aim,the study includes an evaluation based on exams conducted for the routine follow-up of incident patients.

Each incident patient will be followed during 2 years at least.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Patients newly diagnosed with:
  • •Pre capillary pulmonary hypertension at right heart sided catheterization with: mPAP > or = 25 mmHg, PCWP < or = 15 mmHg
  • •Interstitial lung disease with diffuse infiltrative opacities on chest CT scan

Exclusion Criteria

  • •Pulmonary hypertension related to a thromboembolic disease
  • •Respiratory disease other than diffuse interstitial lung disease
  • •Any etiological factor of pulmonary arterial hypertension based on NICE 2013 classification other than diffuse interstitial lung disease
  • •Any progressive disease associated to a life expectancy less than 6 months other than pulmonary hypertension, diffuse interstitial lung disease and respiratory insufficiency

Outcomes

Primary Outcomes

Overall survival

Time Frame: 2 years

Determine predictive factors of mortality

Secondary Outcomes

  • Progression-free survival(2 years)
  • Response to therapy(2 years)

Investigators

Sponsor
Groupe d'Etudes et de Recherche sur les Maladies Orphelines Pulmonaires
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Vincent COTTIN

Professor Vincent COTTIN

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

Study Sites (1)

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