NCT00743158撤回不适用
Transfer Impedance in Cystic Fibrosis (Ztr)
适应症
试验速览
- 阶段
- 不适用
- 状态
- 撤回
- 试验地点
- 1
研究概览
简要总结
This study aims to determine whether respiratory system transfer impedance (Ztr) may fill an important clinical function by providing a reproducible, valid, and sensitive measure of airway obstruction in people with CF.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Only
- 时间视角
- Prospective
入排标准
- 年龄范围
- 2 Years 至 25 Years(Child, Adult)
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Between the ages of 2 to 25 Confirmed diagnosis of Cystic Fibrosis
排除标准
- 未提供
研究者
Thomas Martin
Assistant Professor of Pediatrics
Boston Children's Hospital
研究点 (1)
Loading locations...
相似试验
招募中
不适用
Nasal Potential Difference (NPD) Protocol in Chronic RhinosinusitisRhinosinusitisNCT02038166University of Alabama at Birmingham20
终止
2 期
Study of Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of QBW251 in Subjects With BronchiectasisBronchiectasisNCT04396366Novartis Pharmaceuticals42
已完成
2 期
Study of the Effect of VX-770 on Hyperpolarized Helium-3 Magnetic Resonance Imaging in Subjects With Cystic Fibrosis and the G551D MutationCystic FibrosisNCT01161537Vertex Pharmaceuticals Incorporated13
已完成
2 期
Nasal Potential Studies Utilizing Cystic Fibrosis Transmembrane Regulator (CFTR) ModulatorsCystic FibrosisNCT01348204University of Alabama at Birmingham32
已完成
不适用
Thoracic Mobility in Cystic Fibrosis CareCystic FibrosisNCT04696198Göteborg University63
