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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT03954574
Registration number
NCT03954574
Ethics application status
Date submitted
14/03/2019
Date registered
17/05/2019
Titles & IDs
Public title
Pulmonary Hemodynamics During Exercise - Research Network
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Scientific title
Pulmonary Hemodynamics During Exercise - Research Network
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Secondary ID [1]
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30-437 ex 17/18
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Universal Trial Number (UTN)
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Trial acronym
PEX-NET
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Pulmonary Circulation Diseases
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Condition category
Condition code
Intervention/exposure
Study type
Observational [Patient Registry]
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Diagnosis / Prognosis - assessment of pulmonary hemodynamics during exercise by right heart catheterization
Retrospective patient cohort -
Prospective patient cohort -
Diagnosis / Prognosis: assessment of pulmonary hemodynamics during exercise by right heart catheterization
all patients undergo right heart catheterization during exercise due to clinical reasons. Results of this and other Routine clinical tests will be included in the registry
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Intervention code [1]
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Diagnosis / Prognosis
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Number of Participants who die during observation
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Assessment method [1]
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The investigators aim to assess the prognostic relevance of pulmonary hemodynamics during exercise as assessed by right heart catheterization by using a multi-centre approach and to identify independent predictors of adverse events. Separate data sets will be analysed for the retrospective and prospective Evaluation.
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Timepoint [1]
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6 years
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Primary outcome [2]
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Number of Participants undergoing lung Transplantation during observation
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Assessment method [2]
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Occurrences of lung transplantations
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Timepoint [2]
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6 years
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Secondary outcome [1]
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Number of Participants being hospitalized during observation
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Assessment method [1]
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Number of hospitalizations
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Timepoint [1]
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6 years
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Secondary outcome [2]
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Number of Participants who develop pulmonary Hypertension as assessed by right heart catheterization
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Assessment method [2]
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Diagnosis of pulmonary hypertension
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Timepoint [2]
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6 years
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Secondary outcome [3]
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Number of Participants with newly initiated pulmonary arterial Hypertension medication during observation
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Assessment method [3]
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Evaluation of medication initiations
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Timepoint [3]
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6 years
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Eligibility
Key inclusion criteria
* Patients (females and males; age: above 18yrs) with intermediate or high echocardiographic probability of PH and/or unexplained dyspnea, and/or associated conditions for PAH as clinical indication for RHC at rest and exercise
* Written informed consent of participating subjects after being fully briefed (for prospective analysis)
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* Patients with incomplete hemodynamic data at rest or exercise
* Patients without sufficient follow-up data (information on survival / lung transplantation)
* advanced tumour disease or other diseases with a short life expectancy, except pulmonary vascular diseases
* advanced heart failure with pulmonary arterial wedge pressure (PAWP) > 18 mmHg at rest
* uncontrolled systemic arterial hypertension (RR values > 160/100 mmHg at rest)
* FEV1<50% predicted
* TLC<60% predicted
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Study design
Purpose
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Duration
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Selection
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/12/2018
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
31/12/2029
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Actual
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Sample size
Target
1500
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Recruitment hospital [1]
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Royal Prince Alfred Hospital, Respiratory Medicine - Camperdown
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Recruitment postcode(s) [1]
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- Camperdown
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Recruitment outside Australia
Country [1]
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United States of America
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State/province [1]
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Arizona
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Country [2]
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United States of America
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State/province [2]
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California
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United States of America
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Maryland
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United States of America
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Massachusetts
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Minnesota
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Country [6]
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United States of America
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State/province [6]
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South Carolina
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Country [7]
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Austria
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State/province [7]
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Graz
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Country [8]
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Belgium
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State/province [8]
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Brussels
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Country [9]
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Brazil
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State/province [9]
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São Paulo
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Denmark
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Aarhus
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France
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State/province [11]
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Nancy
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France
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Paris
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Germany
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Cologne
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Germany
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State/province [14]
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Gießen
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Germany
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Greifswald
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Germany
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Heidelberg
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Country [17]
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Germany
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State/province [17]
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Würzburg
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Italy
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Bologna
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Italy
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Roma
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Netherlands
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Amsterdam
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Poland
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Otwock
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Spain
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Barcelona
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Switzerland
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Zürich
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United Kingdom
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Glasgow
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United Kingdom
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London
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Country [26]
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United Kingdom
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State/province [26]
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Sheffield
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Funding & Sponsors
Primary sponsor type
Other
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Name
Medical University of Graz
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Address
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Country
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Other collaborator category [1]
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Other
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Name [1]
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European Respiratory Society
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Address [1]
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Country [1]
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Ethics approval
Ethics application status
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Summary
Brief summary
The purpose of this Clinical Research Collaboration is to investigate the prognostic implications of pulmonary hemodynamics during exercise based on a large scale multi-centre approach by using retrospective and prospective analysis of hemodynamic data.
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Trial website
https://clinicaltrials.gov/study/NCT03954574
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Horst Olschewski, MD
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Address
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Medical University of Graz
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Gabor Kovacs, MD
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Address
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Country
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Phone
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+43-316-385
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
Undecided
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No/undecided IPD sharing reason/comment
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT03954574