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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05965128
Other study ID # KY2022-955
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 1, 2022
Est. completion date December 2027

Study information

Verified date July 2023
Source Huashan Hospital
Contact Wenhong Zhang, M.D.
Phone 13801844344
Email zhangwenhong@fudan.edu.cn
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Relying on fever clinics, this project evaluates the clinical diagnostic efficiency of the three-level pathogen diagnostic system, monitors changes in respiratory pathogens, and realizes real-time monitoring and early warning of acute respiratory infectious diseases in Shanghai.


Description:

This study mainly includes subjects who enter the outpatient and emergency departments, fever clinics, and wards of each center from December 2022. According to the clinical manifestations and epidemiological information of the patients, different step-by-step detection methods will be adopted to optimize the allocation of clinical resources and improve the quality of life. This study aims to improve pathogen diagnosis efficiency and achieve regional respiratory early warning.


Recruitment information / eligibility

Status Recruiting
Enrollment 1255
Est. completion date December 2027
Est. primary completion date December 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 12 Years to 100 Years
Eligibility Inclusion Criteria: 1. Acute onset within one week; 2. 18-70 years old; 3. Present with pneumonia (present with pulmonary signs or radiological changes) or influenza-like illness (including the following symptoms: sudden onset of fever (>38 ?),plus cough and/or other respiratory symptoms such as shortness of breath plus one or more systemic symptoms (fatigue, headache ect.)) Exclusion Criteria: 1. Unable to collect nasal/nasopharyngeal swab/wash/aspirate due to structural disorder or mental problem. 2. Patients with psycological problem or unconsciousness who cannot tell the disease history and cooperate with medical examinations;

Study Design


Locations

Country Name City State
China Heilongjiang Provincial Hospital Harbin Heilongjinag
China People's Hospital of Inner Mongolia Autonomous Region Hohhot Inner Mongolia
China Shandong University Qilu Hospital Jinan Shandong
China Jining Public Health Center Jining Shandong
China The First People's Hospital of Yunnan Province Kunming Yunnan
China Gansu Provincial People's Hospital Lanzhou Gansu
China Ruian City People's Hospital Rui'an Zhejiang
China Fudan University Affiliated Huashan Hospital Shanghai Shanghai
China Shenyang Sixth People's Hospital Shenyang Liaoning
China The First Affiliated Hospital of Suzhou University Suzhou Jiangsu
China The First Hospital of Shanxi Medical University Taiyuan Shanxi
China Affiliated Hospital of Xuzhou Medical University Xuzhou Jiangsu

Sponsors (1)

Lead Sponsor Collaborator
Huashan Hospital

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary the detectioin rate of pathogenic microorganism in each step the detectioin rate of pathogenic microorganism in each step 48 hours
Secondary hospitalization rate hospitalization rate 48 hours
Secondary rate of critical illness rate of critical illness 48 hours
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