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NCT03269630 Clinical Trial

New Orleans Pulmonary Hypertension Biobank

Healthy Clinical Trial

— NO-PH Biobank  

Official title:
New Orleans Pulmonary Hypertension Biobank

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT03269630
Other study ID # LSU
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 29, 2017
Est. completion date October 2027

Study information
Verified date September 2021
Source Louisiana State University Health Sciences Center in New Orleans
Contact Matthew R Lammi, MD, MSCR
Phone 5045684634
Email mlammi@lsuhsc.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Pulmonary hypertension (PH) is a serious condition characterized by a mean pulmonary artery pressure >=25mmHg on right heart catheterization (RHC). Despite advances in PH care, outcomes are still sub-optimal and further research is required into the pathobiology of the disease and development of biomarkers that can guide clinical care. The investigators are establishing a biobank to collect samples (blood, urine, stool) from patients with pulmonary hypertension, patients at high risk for pulmonary hypertension, healthy controls, and patients undergoing right heart catheterization. Specimens will be stored for future investigations.

Recruitment information / eligibility
Status Recruiting
Enrollment 450
Est. completion date October 2027
Est. primary completion date October 2027
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Diagnosis of pulmonary hypertension and followed at the Comprehensive Pulmonary Hypertension Center OR - Diagnosis of systemic sclerosis and followed at the Comprehensive Pulmonary Hypertension Center OR - Diagnosis of mixed connective tissue disease and followed at the Comprehensive Pulmonary Hypertension Center OR - Undergoing outpatient right heart catheterization Exclusion Criteria: - Age<18 - Pregnant - Unable to understand English - Currently incarcerated - Unwilling or unable to sign informed consent

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• No intervention. Biospecimen collection only
Biospecimen collection

Locations
Country Name City State
United States University Medical Center-New Orleans New Orleans Louisiana

Sponsors (1)
Lead Sponsor Collaborator
Louisiana State University Health Sciences Center in New Orleans

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Collection of biospecimens Biospecimen collection only 10 years
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