RecruitingPulmonary Hypertension Due to Lung Diseases and HypoxiaPulmonary HypertensionInterstitial Lung Disease
DeciPHer-ILD: A Real-world Patient Registry in Group 3 Pulmonary Hypertension Associated With Interstitial Lung Disease (PH-ILD)
Eligible age
18+ yrs
Accepts
All genders
Locations
32 states
Healthy volunteers
No
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About this study
This is a prospective, real world, multicenter, registry of patients with pulmonary hypertension associated with interstitial lung disease (PH-ILD) and interstitial lung disease (ILD).
Sponsor: United Therapeutics
You may qualify if…
- ✓ 1. Adults aged 18 years or older
- ✓ 2. Diagnosis of fibrotic ILD based on high-resolution computed tomography imaging, including but not limited to:
- ✓ 1. Idiopathic interstitial pneumonia, including idiopathic pulmonary fibrosis
- ✓ 2. Autoimmune ILD
- ✓ 3. Chronic hypersensitivity pneumonitis
- ✓ 4. Nonspecific interstitial pneumonia
- ✓ 5. Occupational lung disease
- ✓ 6. Combined pulmonary fibrosis and emphysema with fibrosis greater than the extent of emphysema on lung imaging as determined by the Investigator
You may not qualify if…
- ✕ 1. Confirmed diagnosis of Group 1, 2, 4, or 5 PH
- ✕ a. In cases in which a patient has a diagnosis of PH-ILD along with a concomitant diagnosis of another PH group (eg, Group 1), enrollment may be permitted at the Investigator's discretion if, in their clinical judgment, PH-ILD is the predominant driver of the patient's PH.
- ✕ 2. Confirmed diagnosis of Group 3 PH associated with lung diseases and or hypoxia other than fibrotic ILD, as outlined in Inclusion Criterion 2.
- ✕ 3. Patients receiving inhaled treprostinil (Yutrepia™) at Baseline. Patients receiving other forms of PH therapy will be eligible for enrollment.
Where it's recruiting
Alabama
Birmingham
Arizona
Phoenix
California
Los Angeles · Sacramento
Colorado
Aurora · Denver
District of Columbia
Washington D.C.
Florida
Gainesville · Naples · Orlando · Sarasota …
Georgia
Atlanta · Columbus
Illinois
Chicago · Maywood · Oak Lawn
Indiana
Indianapolis
Kansas
Kansas City
Kentucky
Louisville
Louisiana
New Orleans
Source: ClinicalTrials.gov · NCT06388421 · last updated 2026-08-26