Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT03269630

New Orleans Pulmonary Hypertension Biobank

Led by Louisiana State University Health Sciences Center in New Orleans · Updated on 2021-09-10

450

Participants Needed

1

Research Sites

509 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

New Orleans Pulmonary Hypertension Biobank

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosis of pulmonary hypertension and followed at the Comprehensive Pulmonary Hypertension Center
  • Diagnosis of systemic sclerosis and followed at the Comprehensive Pulmonary Hypertension Center
  • Diagnosis of mixed connective tissue disease and followed at the Comprehensive Pulmonary Hypertension Center
  • Undergoing outpatient right heart catheterization
Not Eligible

You will not qualify if you...

  • Younger than 18 years
  • Pregnant
  • Unable to understand English
  • Currently incarcerated
  • Unwilling or unable to sign informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

University Medical Center-New Orleans

New Orleans, Louisiana, United States, 70112

Actively Recruiting

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Research Team

M

Matthew R Lammi, MD, MSCR

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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