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临床试验/NCT01935726
NCT01935726已完成不适用

Pulmonary Fibrosis Contact Registry

National Jewish Health1 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2013年8月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
300
试验地点
1
主要终点
Number enrolled

研究概览

简要总结

As the name states, contact registries securely store contact information from groups of reasonably well-characterized patients (or primary supporters/caregivers) who are interested in being informed about ongoing or future research opportunities. Pulmonary fibrosis (PF) is a condition for which effective therapies have remained elusive, making drug trials and interventional research studies a mainstay in the PF arena over the last decade and for the foreseeable future. A PF Contact Registry will be a conduit to collect, analyze, and disseminate de-identified, group-level data on the clinical phenotypes of PF patients and will house contact information from patients who wish to be informed about research opportunities for which they may qualify. Data contained in the Registry will help inform research hypotheses and guide investigators as they develop research protocols by providing them with numbers of potential subjects who meet particular inclusion/exclusion criteria.

详细描述

Detailed information can be found at our website at www.pulmonaryfirbrosisresearch.org.

Who will be in the Registry?

Anyone who is at least 18 years of age, can read and understand English, and either

  1. diagnosed with PF or
  2. a primary supporter or caregiver of someone living with PF

How the Registry works

研究设计

研究类型
Observational
观察模型
Other
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

  • Anyone who self-reports a diagnosis of pulmonary fibrosis and is over 18 years of age will be included in the Registry.
  • Anyone who self-reports being a primary supporter or caregiver of someone living with pulmonary fibrosis and is over the age of 18 will be included in the Registry.
  • Whoever consents to be enrolled in the Registry will presumably be able to read and write in English.

排除标准

  • Failure to meet inclusion criteria

结局指标

主要结局

Number enrolled

时间窗: 20 years

This is a contact registry. We will enroll as many patients and primary supporters/caretakers as possible.

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

Jeff Swigris

Associate Professor of Medicine

National Jewish Health

研究点 (1)

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