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临床试验/NCT04808596
NCT04808596招募中不适用

Pulmonary Hypertension Biorepository and Registry

University of Kansas Medical Center1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2020年8月10日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
300
试验地点
1
主要终点
Establish a Biorepository

研究概览

简要总结

Establish a pulmonary hypertension registry and biorepository to lead towards a further understanding of the disease.

详细描述

The aim of this project will be to establish a broad and wide-ranging registry and biorepository of blood samples from patients with pulmonary hypertension, including all WHO groups I-V to be used for future research in these areas. This will be both a retrospective and prospective project. The registry and biorepository will be utilized to study and grow our knowledge of the cellular mechanisms and mediators of the disease and, in turn, contribute to advancements in treatment.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • The participant is a patient at TUKHS or has agreed to participate in a study approved by the KUMC Human Research Protection Program (HRPP)
  • The participant has a diagnosis of pulmonary hypertension confirmed by right heart catheterization
  • Patient is ≥ 18 years of age or older

排除标准

  • Participant declines to participate (living patients only)
  • Participant is unable to provide informed consent (living patients only)

结局指标

主要结局

Establish a Biorepository

时间窗: From Enrollment to 6 Months

Establish a collection of biospecimens from patients with pulmonary hypertension.

Collaborate

时间窗: From Enrollment to 24 Months

Provide biospecimens to researchers investigating pulmonary hypertension. Separate IRB approval will be needed for these studies.

Biospecimens Collection

时间窗: From Enrollment to 12 Months

Correlate biospecimens to longitudinally collected individual patient data.

Collect Clinical Data

时间窗: From Enrollment to 6 Months

Collect clinically obtained data from current and deceased patients with pulmonary hypertension to support research.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Leslie Spikes, MD

Associate Professor

University of Kansas Medical Center

研究点 (1)

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