: Center for pulmonary Hypertension, Thoraxclinic Heidelberg Trials

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Trial + Data / Events

Status

Region

Interventions

Sponsor

Conditions

Primary compl

Study compl

Gruenig, Ekkehard

NCT03626688 / 2018-001187-33: A Study Evaluating the Efficacy and Safety of Ralinepag to Improve Treatment Outcomes in PAH Patients

Recruiting

1000

Europe, Canada, US, RoW

Ralinepag, APD811, Placebo

United Therapeutics

PAH, Pulmonary Hypertension, Pulmonary Arterial Hypertension, Hypertension, Connective Tissue Diseases, Familial Primary Pulmonary Hypertension, Vascular Diseases, Cardiovascular Diseases, Hypertension, Pulmonary, Lung Diseases, Respiratory Tract Disease

12/24

IMPAHCT-FUL, NCT05557942 / 2021-006864-25: Inhaled Imatinib Pulmonary Arterial Hypertension Clinical Trial - Follow Up Long Term Extension

Terminated

186

Europe, Canada, US, RoW

AV-101

Aerovate Therapeutics, Aerovate Therapeutics Inc

Pulmonary Arterial Hypertension

08/24

IMPAHCT, NCT05036135: A Study of AV-101 (Dry Powder Inhaled Imatinib) in Patients With Pulmonary Arterial Hypertension (PAH)

Terminated

2/3

202

Europe, Canada, US, RoW

AV-101, Placebo

Aerovate Therapeutics

Pulmonary Arterial Hypertension

08/24

NCT00477724: Latent Pulmonary Hypertension (PH) in Chronic Thromboembolic Pulmonary Hypertension (CTEPH )After Endarterectomy and Influence of Exercise and Respiratory Therapy

Recruiting

N/A

Europe

exercise and respiratory therapy, sedentary control group

Heidelberg University

Pulmonary Hypertension, Chronic Thromboembolic Pulmonary Hypertension

12/23

NCT00491309: Exercise and Respiratory Therapy in Patients With Rheumatoid Arthritis / Collagenosis and Pulmonary Hypertension

Recruiting

N/A

Europe

exercise training

Heidelberg University

Pulmonary Hypertension, Connective Tissue Disease

12/23

NCT01397110: Respiratory and Physical Therapy in Patients With Associated Pulmonary Arterial Hypertension (APAH) With Congenital Heart Defects

Recruiting

N/A

Europe

respiratory and exercise therapy

Heidelberg University

Pulmonary Arterial Hypertension, Eisenmenger Syndrome

12/25



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