Pulmonary Fibrosis Contact Registry
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
- diagnosed with PF or
- 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
- 是
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
Jeff Swigris
Associate Professor of Medicine
National Jewish Health
