Pulmonary Hypertension (PH) Biorepository for Translational Research

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-100
SponsorNational Institutes of Health Clinical Center (CC)

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Provision of signed and dated informed consent form

Males and females aged >=18 years old

Suspected of or diagnosed with PH

Able to understand and willing to sign a written informed consent document

Disqualifiers

None

Trial population

The study population will consist of adult male and female participants older than 18 years who are suspected of having or have been diagnosed with pulmonary hypertension (PH). Eligible individuals must be able to understand the study requirements and be willing to provide written informed consent by signing and dating the informed consent form prior to participation.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

1,000 Participants
are grouped into 5 trial groups
Group A: Group 1 (suspected of or diagnosed)
Group B: Group 2 (suspected of or diagnosed)
Group C: Group 3 (suspected of or diagnosed)
Group D: Group 4 (suspected of or diagnosed)
Group E: Group 5 (suspected of or diagnosed)

Trial outcomes

Primary outcomes

1

Develop a multi-center biorepository.

Develop a multi-center biorepository of patients suspected of or diagnosed with PH Group 1-5.

Time frame
10 years

Secondary outcomes

1

Collect the specific data attributes in combination with clinical data to be used in the future to determine multimodal genomic, metabolomic or proteomic biomarkers.

This research may predict clinically relevant outcomes. Elucidate molecular phenotypes that distinguish between patients across PH groups

Time frame
10 years

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: