Pulmonary Hypertension (PH) Biorepository for Translational Research

NCT07647549 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2026-08-11

No results posted yet for this study

Summary

Background:

Pulmonary hypertension (PH) is high blood pressure in the blood vessels of the lungs. It can lead to heart failure and death if not treated. Researchers want to create a repository of blood samples and health information collected from people with PH. They hope to use this information to find better ways to diagnose and treat PH.

Objective:

To collect blood samples and health information from people suspected of or diagnosed with PH.

Eligibility:

People aged 18 years and older who have or may have PH.

Design:

Researchers will collect information from participants medical records.

Participants will have blood drawn from a vein. About 3 tablespoons will be collected during the study visit. The visit will last about 1 hour.

Participants may choose to provide new blood samples at follow-up visits. Updated medical information may also be collected.

Participants may continue to participate as long as the study is ongoing. Participants may opt out of providing new blood samples but remain in the study.

All study samples will be stored at the National Institutes of Health. Health information will be stored in secure databases.

Conditions

Sponsors & Collaborators

  • National Institutes of Health Clinical Center (CC)

    lead NIH

Principal Investigators

  • Michael A Solomon, M.D. · National Institutes of Health Clinical Center (CC)

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-08-16
Primary Completion
2036-06-01
Completion
2036-06-01

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07647549 on ClinicalTrials.gov