Pulmonary Hypertension Registry Switzerland
Swiss PH Registry - Cohort of Swiss PH Patients
1 other identifier
observational
1,000
1 country
1
Brief Summary
Registry Data from PH-patients in Switzerland, who have given consent to records for research purposes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jun 2017
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
June 1, 2017
CompletedFirst Submitted
Initial submission to the registry
November 1, 2022
CompletedFirst Posted
Study publicly available on registry
November 9, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2027
November 9, 2022
November 1, 2022
10.5 years
November 1, 2022
November 8, 2022
Conditions
Outcome Measures
Primary Outcomes (1)
6-minute walking distance
6-minute walking distance
within the study duration e.g. up to 10 years
Secondary Outcomes (4)
New York Heart Association functional class
within the study duration e.g. up to 10 years
NTproBNP
within the study duration e.g. up to 10 years
Survival
within the study duration e.g. up to 10 years
Medication
within the study duration e.g. up to 10 years
Study Arms (5)
Pulmonary arterial hypertension
Pulmonary arterial hypertension
PH due to left heart diseases
PH due to left heart diseases
PH due to lung disease and/or hypoxia
PH due to lung disease and/or hypoxia
Chronic thromboembolic PH
Chronic thromboembolic PH
Miscellaneous PH
Miscellaneous PH
Eligibility Criteria
Pulmonary Hypertension (PH)
You may qualify if:
- Patients with PH
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Zurichlead
- Actelioncollaborator
Study Sites (1)
Respiratory Clinic, University Hospital of Zurich
Zurich, 8091, Switzerland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Silvia Ulrich, Prof. Dr.
UniversityHospital Zurich
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 10 Years
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 1, 2022
First Posted
November 9, 2022
Study Start
June 1, 2017
Primary Completion (Estimated)
December 1, 2027
Study Completion (Estimated)
December 1, 2027
Last Updated
November 9, 2022
Record last verified: 2022-11
Data Sharing
- IPD Sharing
- Will not share