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临床试验/NCT05161858
NCT05161858已完成不适用

Longitudinal Characterization of Respiratory Tract Exacerbations and Treatment Responses in Primary Ciliary Dyskinesia

University of North Carolina, Chapel Hill7 个研究点 分布在 2 个国家目标入组 105 人开始时间: 2022年3月29日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
105
试验地点
7
主要终点
Mean FEV1 Percent Predicted Values in Well State and Sick State

研究概览

简要总结

The overall objective of this longitudinal, observational study is to provide information needed to inform the design of future interventional trials of respiratory exacerbation prevention and treatment in children and adults with primary ciliary dyskinesia (PCD).

详细描述

This is a longitudinal, prospective multicenter study to characterize acute respiratory illnesses (ARIs) and response to treatment in PCD patients. Participants (N=125) will be children age ≥6 years and adults with definite PCD. Participants will be enrolled for approximately 13 months, during which they will attend at least two study visits and perform home monitoring. Participants will be encouraged to attend study visits in-person but will have the option for virtual telehealth visits to ensure compliance with local guidelines and participant safety. Endpoints will be assessed during both well state (i.e., patients typical state of health) and sick state (i.e., during each self-reported period of acute respiratory illness). Informed consent will be obtained, after which the participant will be receive a home spirometer and instructed in its use This design allows for a training period in order to become proficient with home spirometry, with the first study visit occurring 1 month ± 2 weeks after enrollment and the second 12 (±1) months after visit 1 (coordinated with routine clinic visits as possible). Participants will also participate in a set of two optional ARI visits during one ARI, scheduled between 3-5 business days of study team notification by the participant of the new ARI and 2-4 weeks later.

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
6 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of PCD
  • Clinical features consistent with PCD PLUS
  • At least 1 diagnostic test consistent with PCD:
  • i) Biallelic pathogenic variants in PCD-associated genes identified by genetic panel testing including deletion/duplication analysis; ii) Ciliary ultrastructural defect by transmission electron microscopy known to be disease-causing, including outer dynein arm defects, outer dynein arm plus inner dynein arm (IDA) defects, IDA defects with microtubular disorganization and absent central pair
  • Age ≥ 6 years
  • At least one course of antibiotics (oral or IV) in the prior year prescribed to treat new or increased respiratory symptoms
  • Smart phone and/or internet access available in home
  • Informed consent provided by participant or parent/guardian, with assent provided as applicable

排除标准

  • Acute course of antibiotics for respiratory symptoms completed <14 days prior to enrollment or Visit 1 (evaluated at enrollment and Visit 1; visit may be rescheduled >14 days after completion of antibiotics)
  • Developmental or cognitive disability that would impair ability to complete PRO instruments or perform spirometry
  • Congenital heart disease OTHER THAN repaired or resolved atrial septal defect (ASD) or ventricular septal defect (VSD)
  • Asplenia or functional asplenia
  • Co-existing non-pulmonary disease that, in the opinion of the investigator, could have significant impact on lung function or health-related quality of life (e.g., severe scoliosis) or overall health status (e.g., cancer, severe renal disease)
  • Listed for or post-lung transplantation

结局指标

主要结局

Mean FEV1 Percent Predicted Values in Well State and Sick State

时间窗: 12 months

Forced expired volume in 1 second (FEV1) will be assessed by percentage of the predicted value (0-100%).

Mean Primary Ciliary Dyskinesia-Quality of Life Score in Well State and Sick State

时间窗: 12 months

Domains (scales) include physical, emotional, social, school and role functioning; treatment burden; ears and hearing; upper and lower respiratory symptoms; and vitality. The recall period is one week and responses are rated on a 4-point Likert scale.

Mean PCD-Respiratory Symptom Diary Score Well State and Sick State

时间窗: 12 months

The PCD-RSD contains 17 items, 10 on symptoms and 7 on social/emotional impact. The recall period is 24 hours and 15 questions are rated on a 5-point Likert Scale, while two questions are binary (Range: 0-62, 0 being the best and 62 being the worst).

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (7)

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