Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
12 participants
OBSERVATIONAL
2014-07-31
2019-12-31
Brief Summary
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The hypothesis is that the increased use of modern imaging guided tools is essential for the follow up.
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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3D echocardiography
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* pulmonary arterial hypertension WHO group I who are going to start a therapy with prostanoid
* written informed consent
* Prostanoid naive
* no change of the pulmonary arterial hypertension therapy within 3 weeks of inclusion into the study
Exclusion Criteria
* Women of childbearing potential who do not use an effective and secure method for birth control
* severe chronic kidney insufficiency (glomerular filtration rate \<30), which will remain for more than 3 months
* liver insufficiency Child C
* life expectancy shorter than the course of the study (for example because of a malignant disease)
18 Years
ALL
No
Sponsors
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Regina Steringer-Mascherbauer
OTHER
Responsible Party
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Regina Steringer-Mascherbauer
OA Dr.
Principal Investigators
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Regina Steringer-Mascherbauer, MD
Role: PRINCIPAL_INVESTIGATOR
Krankenhaus der Elisabethinen Linz GmbH
Locations
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Krankenhaus der Elisabethinen Linz GmbH
Linz, Upper Austria, Austria
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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Protocol PARIS3D
Identifier Type: -
Identifier Source: org_study_id
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