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临床试验/NCT01769430
NCT01769430已完成不适用

Evaluating Modes of Influenza Transmission Work Package 1: Observational Study of Community Acquired Influenza

University of Maryland, College Park1 个研究点 分布在 1 个国家目标入组 178 人开始时间: 2012年12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
178
试验地点
1
主要终点
Viral Copy Number in 30-minute Exhaled Breath Sample

研究概览

简要总结

The recent swine origin influenza pandemic (2009), new emergence of swine origin H3N2v, and delayed availability of vaccine for these agents highlight the need to test and optimize public health intervention strategies to reduce transmission of influenza. We will use a new technology for biological particle collection (U.S. Provisional Patent Application No. 61/162,395, McDevitt et al., Aerosol Sci Technol 2013) to make fundamental observations on infectious respiratory droplets in a study of up to 200 naturally occurring seasonal influenza cases. We will collect respiratory droplets shed by participants while breathing normally, talking, and spontaneously coughing. We will characterize the size distribution of droplets containing infectious virus. We will use these basic data to examine the roles of large and small respiratory droplets and examine how the interaction of host factors and virus type impact the shedding of infectious respiratory droplets. Subjects will be recruited through a web based respiratory illness surveillance system, health clinics and advertisement in the campus community. Sitting in the collection booth will not create additional discomfort or risk for volunteers already suffering from influenza infection. We will recruit up to 1000 persons with symptoms of acute respiratory illness for screening with collection of nasopharyngeal swabs and questionnaire. From among those screened, we will recruit 250 to give exhaled breath samples, and ask 50 people with influenza to return for follow up exhaled breath samples on up to two subsequent days. We hypothesize that (1) fine aerosols (<5 microns in aerodynamic diameter) will contain more viral copies than coarse aerosol particles (>= 5 microns) (2) fine aerosols will contain culturable virus indicating that the fine aerosols are infectious, (3) aerosol shedding will correlate with virus load measured by swabs, (4) presence of active cough during sampling will be associated with increased aerosol shedding, (5) clinical symptoms and signs, including fever can be used to predict viral aerosol shedding.

详细描述

This study is a follow-on to earlier projects funded by the US Centers for Disease Control and Prevention (CDC) and the National Institute for Allergy and Infectious Diseases (NIAID) that developed the sampler and studied the impact of surgical masks on reducing viral aerosol release by persons infected with influenza virus. The funding organizations have no direct control over the study design, execution, or reporting and no access to identifiable human data. The CDC IRB has determined that the CDC is not engaged in human subjects research in this cooperative agreement.

Hypotheses:

  • Fine particle aerosols will contain greater numbers of viral copies than will coarse aerosol particles.
  • Clinical symptoms and signs, including fever can be used to predict viral aerosol shedding
  • Fine aerosols will contain culturable virus indicating that the fine aerosols are infectious
  • Aerosol shedding will correlate with virus load measured by nasopharyngeal and throat swabs
  • Presence of active cough during sampling will be associated with increased aerosol shedding with a stronger correlation to be found with coarse than fine particle virus aerosols

研究设计

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

入排标准

年龄范围
10 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Presence of symptomatic respiratory infection or other evidence of respiratory infection:
  • During the influenza season, subjects will be enrolled if they have
  • influenza-like illness (symptoms of fever and either cough or sore throat) and either
  • a positive point of care rapid test for influenza infection or
  • objectively documented fever in the setting of a documented local influenza outbreak (presence of rapid test or PCR confirmed cases).
  • Onset within the previous 48 hours
  • Prior to onset of influenza season and if we have not achieved enrollment of our target population by the end of flu season, we will enroll subjects with cough, coryza (stuffy runny nose, sore throat, sneezing), and malaise (fatigue) characteristic of the 'common cold' often resulting from Human Rhinovirus, RSV, parainfluenza, and to some extent influenza virus.

排除标准

  • 未提供

结局指标

主要结局

Viral Copy Number in 30-minute Exhaled Breath Sample

时间窗: Daily measurements on days 1 through 3 post onset of symptoms (each person contributed 1 to a max of 3 samples). Reported values are the geometric mean over all samples and persons.

Total viral RNA copies detected in breath aerosol exhaled during a 30-minute sample collection. Participants sit for 30 minutes with face inside the cone/funnel of the Gesundheit-II (G-II) human bioaerosol collector (https://doi.org/10.1080/02786826.2012.762973) collecting air at 130 L/min. Particles in air are concentrated into a small volume of buffer. The copies per mL of buffer is measured by PCR and corrected to the total amount collected per 30-min sample. See publication in the Proceedings of the National Academy of Sciences (https://doi.org/10.1073/pnas.1716561115) and PLoS Pathogens (https://doi.org/10.1371/journal.ppat.1003205) for more details.

Total Fine Aerosol Infectious Influenza Virus in 30-minute Exhaled Breath Sample

时间窗: Daily measurements on days 1 through 3 post onset of symptoms (each person contributed 1 to a max of 3 samples). Reported values are the geometric mean over all samples and persons.

Fluorescent Focus Assay detection of infectious influenza virus in Fine Particle (≤5 µm) aerosol reported as fluorescent focus units (FFU) per 30-minute breath sample. Aerosol samples were collected at 130 L/min for 30 minutes by an aerosol sampler that concentrated the aerosol in a small volume of liquid. The FFU/ml were multiplied by the volume of liquid in the final concentrate sample to obtain the total infectious particles per 30-minute sample. This outcome was peer reviewed and published in the Proceedings of the National Academy of Sciences.

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

Donald K. Milton

Professor of Environmental Health, School of Public Health

University of Maryland, College Park

研究点 (1)

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