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NCT05776225Completed

Pulmonary Hypertension Screening in Patients With Interstitial Lung Disease for Earlier Detection

Pulmonary Hypertension Screening in Patients With Interstitial Lung Disease for Earlier Detection (PHINDER)

Source: ClinicalTrials.gov · Last updated 28 May 2026

Brief summary (registry, in English)

Study GMS-PH-001 is a multicenter, open-label, non-randomized study to prospectively evaluate screening strategies of pulmonary hypertension (PH) in patients with interstitial lung disease (ILD).

Status (registry)
Completed
Study type
Observational
Enrollment
314 (actual)
First submitted
1 Mar 2023
Start date
11 Aug 2023
Primary completion date
13 Mar 2026
Lead sponsor
United Therapeutics
NCT number
NCT05776225

What you commit to

  • Study type: Observational
  • Participants enrolled: 314
  • From 11 Aug 2023 to the primary completion date, 13 Mar 2026
  • 42 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior RHC with mPAP \>20 mmHg.
  • Currently on a Food and Drug Administration (FDA)-approved pulmonary arterial hypertension (PAH) medication for the treatment of PAH.

Other illness

  • Diagnosed with chronic obstructive pulmonary disease (CPFE with mild emphysema notwithstanding).

Lab values

  • History of ischemic heart disease or left-sided myocardial dysfunction within 12 months of Screening, defined as left ventricular ejection fraction \<40% or pulmonary capillary wedge pressure \>15 mmHg.

Other

  • Uncontrolled or untreated moderate to severe sleep apnea as determined by the patient's physician.
  • Pulmonary embolism within the past 3 months.
  • Any other clinical features that, in the opinion of the Investigator, might adversely affect interpretation of study data or study safety, or make the patient unsuitable for RHC or HRCT (e.g., pregnancy).

Who the study is looking for

  • Patient gives voluntary written informed consent to participate in the study and are capable of reading and understanding questionnaires or forms in English or Spanish.
  • Patients with a diagnosis of ILD based on computed tomography imaging, including:
    • Idiopathic interstitial pneumonia, including idiopathic pulmonary fibrosis
    • Connective tissue disease-associated ILD with forced vital capacity (FVC) \<70%
    • Hypersensitivity pneumonitis
    • Scleroderma-related ILD
    • Autoimmune ILD
    • Nonspecific interstitial pneumonia
    • Occupational lung disease
    • Combined pulmonary fibrosis and emphysema with mild emphysema on lung imaging as determined by the Investigator
  • Patients must have at least 2 signs or symptoms suggestive of PH, as specified by the study protocol.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (42)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
AnMed Health Pulmonary and Sleep Medicine
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AndersonUnited StatesUnknown status
University of Michigan Int Med Pulmonary and Critical Care
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Ann ArborUnited StatesUnknown status
Emory University Hospital
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AtlantaUnited StatesUnknown status
Piedmont Healthcare
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AustellUnited StatesUnknown status
St. Luke's University Health Network
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BethlehemUnited StatesUnknown status
The University of Vermont Medical Center
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BurlingtonUnited StatesUnknown status
University of Virginia
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CharlottesvilleUnited StatesUnknown status
Loyola University Chicago
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ChicagoUnited StatesUnknown status
Northwestern University
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ChicagoUnited StatesUnknown status
Prisma Health
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ColumbiaUnited StatesUnknown status
Premier Pulmonary Critical Care and Sleep Medicine
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DenisonUnited StatesUnknown status
Duke University Medical Center
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DurhamUnited StatesUnknown status
Inova Fairfax Hospital
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Falls ChurchUnited StatesUnknown status
Northshore University Health System
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GlenviewUnited StatesUnknown status
PulmonIx, LLC
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GreensboroUnited StatesUnknown status
East Carolina University
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GreenvilleUnited StatesUnknown status
Blessing Health Hannibal
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HannibalUnited StatesUnknown status
Hartford Hospital
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HartfordUnited StatesUnknown status
Houston Methodist Hospital
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HoustonUnited StatesUnknown status
Marshall Health
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HuntingtonUnited StatesUnknown status
Statcare Pulmonary Consultants
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KnoxvilleUnited StatesUnknown status
Lakeland Regional Health
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LakelandUnited StatesUnknown status
Dartmouth Hitchcock Medical Center
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LebanonUnited StatesUnknown status
University of Kentucky Medical Center
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LexingtonUnited StatesUnknown status
Medical College of Wisconsin
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MilwaukeeUnited StatesUnknown status
Intermountain Healthcare
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MurrayUnited StatesUnknown status
NCH Healthcare System
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NaplesUnited StatesUnknown status
Jersey Shore University Medical Center
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Neptune CityUnited StatesUnknown status
LSU Health Sciences Center - New Orleans
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New OrleansUnited StatesUnknown status
NYU Langone Medical Center
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New YorkUnited StatesUnknown status
Sentara Cardiovascular Research Institute
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NorfolkUnited StatesUnknown status
Mclaren Greater Lansing
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OkemosUnited StatesUnknown status
Pulmonary Associates
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PhoenixUnited StatesUnknown status
Legacy Health
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PortlandUnited StatesUnknown status
Renown Regional Medical Center
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RenoUnited StatesUnknown status
Pulmonary Associates of Richmond
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RichmondUnited StatesUnknown status
University Of Utah Health
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Salt Lake CityUnited StatesUnknown status
The University of Texas Health Science Center at San Antonio
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San AntonioUnited StatesUnknown status
Providence Medical Research Center
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SpokaneUnited StatesUnknown status
University of South Florida Health
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TampaUnited StatesUnknown status
Montefiore Medical Center
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The BronxUnited StatesUnknown status
Cleveland Clinic Florida
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WestonUnited StatesUnknown status

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This page is information, not medical advice. Discuss any trial with your doctor.