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Plaučių hipertenzija klinikiniai tyrimai Utah

7 tyrimai dėl Plaučių hipertenzija ieško dalyvių vietose Utah.

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Oficialus tyrimo tekstas (anglų kalba)

Efficacy and Safety Study of Treprostinil Palmitil Inhalation Powder (TPIP) in Participants With Pulmonary Hypertension Associated With Interstitial Lung Disease (PH-ILD)

  • USA025, Salt Lake City
Renkami dalyviai3 fazė
Amžius 18 ir vyresni · Visoms lytims · Atnaujinta 2026-09-29 · NCT07179380

Multi-site Study of the Clinical Impact of an AI-assisted Approach to Referring Patients With Interstitial Lung Disease for Diagnostic Evaluation of Pulmonary Hypertension

  • University of Utah, Salt Lake City
Renkami dalyviai
Amžius 18 ir vyresni · Visoms lytims · Atnaujinta 2026-09-02 · NCT06911632

DeciPHer-ILD: A Real-world Patient Registry in Group 3 Pulmonary Hypertension Associated With Interstitial Lung Disease (PH-ILD)

  • Intermountain Medical Center, Murray
  • University of Utah Health, Salt Lake City
Renkami dalyviaiStebimasis tyrimas
Amžius 18 ir vyresni · Visoms lytims · Atnaujinta 2026-08-26 · NCT06388421

De-implementing Inhaled Nitric Oxide for Congenital Diaphragmatic Hernia

  • University of Utah & Primary Children's Hospital (Utah-PCH), Salt Lake City
Renkami dalyviai4 fazė
0 Months – 1 Month · Visoms lytims · Atnaujinta 2026-08-18 · NCT05213676

Trial to Evaluate Safety And Effectiveness of Mechanical Circulatory Support in Patients With Advancing Heart Failure

  • University of Utah Hospital, Salt Lake City
Renkami dalyviai
Amžius 18 ir vyresni · Visoms lytims · Atnaujinta 2026-06-10 · NCT06526195

Pulmonary Hypertension Association Registry

  • University of Utah Health, Salt Lake City
Renkami dalyviaiStebimasis tyrimas
Amžius 0 ir vyresni · Visoms lytims · Atnaujinta 2025-11-14 · NCT04071327

A Trial of Phosphodiesterase-5 Inhibitor in Neonatal Congenital Diaphragmatic Hernia (TOP-CDH)

  • Primary Children's Hospital, Salt Lake City
Renkami dalyviai2 fazė
Visi amžiai · Visoms lytims · Atnaujinta 2025-04-04 · NCT05201144

Iš ClinicalTrials.gov, duomenys gauti 2026-10-05. Kiekvienas tyrimas nustato savo tinkamumo kriterijus; tyrimo komanda sprendžia, kas gali dalyvauti.