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Clinical Trials/NCT03269630
NCT03269630
Recruiting
Not Applicable

New Orleans Pulmonary Hypertension Biobank

Louisiana State University Health Sciences Center in New Orleans1 site in 1 country450 target enrollmentDecember 29, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pulmonary Hypertension
Sponsor
Louisiana State University Health Sciences Center in New Orleans
Enrollment
450
Locations
1
Primary Endpoint
Collection of biospecimens
Status
Recruiting
Last Updated
4 years ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
December 29, 2017
End Date
October 2027
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Matthew Lammi

Associate Professor of Medicine

Louisiana State University Health Sciences Center in New Orleans

Eligibility Criteria

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

  • Unable to understand English
  • Currently incarcerated
  • Unwilling or unable to sign informed consent

Outcomes

Primary Outcomes

Collection of biospecimens

Time Frame: 10 years

Biospecimen collection only

Study Sites (1)

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