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临床试验/NCT03684759
NCT03684759已完成不适用

Pilot Feasibility Study for Cystic Fibrosis Sputum Validation for the Molecular Diagnosis of Respiratory Viral Infections

University Hospital, Brest3 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2016年2月24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
30
试验地点
3
主要终点
Concordance of viral type detected in both samples for each participant: sputum and nasopharyngeal swab

研究概览

简要总结

The aim of this pilot study is to demonstrate the feasibility of viral biomolecular diagnosis in sputum compared to nasopharyngeal swab in cystic fibrosis acute respiratory infection.

详细描述

In cystic fibrosis (CF), patients face polymicrobial airway infections. Besides bacteria, viruses are now also considered as important agents in lung function deterioration. No strategy has been established on the optimal sampling for respiratory viral molecular diagnostic in CF. Nasopharyngeal swabs (NP) are recommended for respiratory viral screening in non-CF patients but are invasive and sometimes painful for patients. As sputa are non invasive and collected for bacterial monitoring in CF patients they could represent a convenient alternative to NP swabs.

This study's aim is to define whether viral screening give concordant results between sputa and NP swabs.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Participant with Cystic Fibrosis
  • Participant able to expectorate
  • Participant with sign of acute respiratory infection

排除标准

  • participant not able to expectorate
  • patient refusing to participate

结局指标

主要结局

Concordance of viral type detected in both samples for each participant: sputum and nasopharyngeal swab

时间窗: Day 1

Comparison of per participant results of viral molecular detection in sputum and nasopharyngeal swab. Concordance=same virus(es) or no virus detected in both sample. no concordance=different viruses detected in each sample or virus(es) detected in only one sample and not in the other

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 (3)

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