- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01501838
Pulmonary Hypertension Institutional Registry at Hospital Italiano de Buenos Aires (PH-HIBA)
August 19, 2025 updated by: Ignacio M Bluro, Hospital Italiano de Buenos Aires
The purpose of this study is to create a registry of patients with Pulmonary Hypertension who received medical care in the Hospital Italiano of Buenos Aires.
Study Overview
Status
Recruiting
Conditions
Detailed Description
The Institutional Registry of Pulmonary Hypertension includes patients prospectively with incident pulmonary hypertension type I.
It also includes prevalent cases from our HMO who had diagnosis prior the beginning of the registry.
Study Type
Observational
Enrollment (Estimated)
200
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Ignacio M Bluro, MD
- Phone Number: 5303 +541149590200
- Email: ignacio.bluro@hospitalitaliano.org.ar
Study Locations
-
-
-
Buenos Aires, Argentina, 1181
- Recruiting
- Hospital Italiano de Buenos Aires
-
Contact:
- Ignacio M Bluro, MD
- Phone Number: 5303 +541149590200
- Email: ignacio.bluro@hiba.org.ar
-
Principal Investigator:
- Ignacio M Bluro, MD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
17 years and older (Child, Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients who meet inclusion criteria and none of exclusion criteria during the study period are eligible to this study.
In the population, the PAH cohort will consist of those incident cases and prevalent cases PAH WHO group 1 aged ≥18 years between January 2017 and December 2030 who attended at Hospital Italiano of Buenos Aires.
Description
Inclusion Criteria:
- Diagnosed with PAH WHO group 1 (2022 ESC/ESR guidelines criteria) as the presence of a mean pulmonary artery pressure (mPAP) greater than 20 mmHg at rest with pulmonary arterial wedge pressure (PAWP) >15 mmHg and pulmonary vascular resistance (PVR) >2 WU, according to the 2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension.
- Included in the institutional registry of PAH of Hospital Italiano de Buenos Aires
- Aged ≥18 years at the index date.
- Exclusion Criteria History of lung transplantation surgery previously the baseline period
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pulmonary Hypertension prevalence
Time Frame: 1 year
|
Pulmonary Hypertension prevalence in our community.
|
1 year
|
|
Pulmonary Hypertension incidence
Time Frame: 1 year
|
Pulmonary Hypertension incidence in our community
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Mortality rate
Time Frame: 1 year
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Ignacio M Bluro, MD, Hospital Italiano de Buenos Aires
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2017
Primary Completion (Estimated)
December 31, 2030
Study Completion (Estimated)
June 1, 2031
Study Registration Dates
First Submitted
June 16, 2011
First Submitted That Met QC Criteria
December 26, 2011
First Posted (Estimated)
December 29, 2011
Study Record Updates
Last Update Posted (Actual)
August 24, 2025
Last Update Submitted That Met QC Criteria
August 19, 2025
Last Verified
August 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 1487
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.