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临床试验/NCT07647549
NCT07647549尚未招募不适用

Pulmonary Hypertension (PH) Biorepository for Translational Research

National Institutes of Health Clinical Center (CC)3 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2026年9月21日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
1,000
试验地点
3
主要终点
Develop a multi-center biorepository.

研究概览

简要总结

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.

详细描述

Study Description:

This study aims to establish a biorepository based on the World Symposium Pulmonary Hypertension (PH) Groups 1-5. In the future, IRB approved protocols may use these blood samples to discover novel, biologically relevant, non-invasive PH biomarkers. In combination with clinical data these potential biomarkers will be used to distinguish PH groups, elucidate underlying molecular phenotypes, predict clinically relevant outcomes, as well as discriminate healthy (healthy subjects will not be enrolled under this protocol) from PH disease states, and differentiate patients with PH from patients without PH. To this end, multimodal genomic, metabolomic, and proteomic assays will eventually be developed and used.

Objectives:

Primary:

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

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • INCLUSION CRITERIA:
  • 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

排除标准

  • Any individual who does not meet all inclusion criteria or is deemed by the local investigator not to be a blood draw candidate will be excluded from participating in this study.

研究组 & 干预措施

Group 5 (suspected of or diagnosed)

PH with unclear or multifactorial mechanisms

Group 1 (suspected of or diagnosed)

Pulmonary Arterial Hypertension, PAH

Group 2 (suspected of or diagnosed)

PH due to left heart disease

Group 3 (suspected of or diagnosed)

PH due to lung diseases and/or hypoxia

Group 4 (suspected of or diagnosed)

PH due to thromboembolic disease

结局指标

主要结局

Develop a multi-center biorepository.

时间窗: 10 years

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

次要结局

  • Collect the specific data attributes in combination with clinical data to be used in the future to determine multimodal genomic, metabolomic or proteomic biomarkers.(10 years)

研究者

申办方类型
Nih
责任方
Sponsor

研究点 (3)

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