RBR-10s75n9x尚未招募未知
sability evaluation of the rapid SARS-CoV-2 antigen detection self-test (COVISTIX/COVIMARK) by lay subjects
CAEP - Centro Avançado de Estudos e Pesquisas0 个研究点开始时间: 2022年5月27日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 尚未招募
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Intervention
入排标准
- 年龄范围
- 18Y 至 0(—)
入选标准
- •Cohort A - Adult subjects over 18 years old, of both sexes; be able to sign the ICF approved by the EC and to execute and understand all the procedures and instructions of the study; presenting suspected flu-like symptoms of COVID-19 with an onset of 5 days or less; or having had contact with a person infected with SARS-CoV-2 within 14 days; Cohort B - Adult subjects over 18 years of age, of both sexes; be able to sign the ICF approved by the EC and execute and understand all assay procedures and instructions; previous positive test for COVID-19 less than 2 days; if the subject is symptomatic for COVID-19, the symptoms are of mild to moderate intensity; be immunized with at least two doses of the COVID-19 vaccine; availability of maintaining isolation for up to 9 days from the signing of the ICF, to perform the self-test at home and home collection of RT-PCR for SARS-CoV-2 at the end of the study; be able to photograph the cassettes with the test result and sending the images to the research center, daily
排除标准
- •Cohort A - Present a diagnosis of COVID-19 with symptoms of severe acute respiratory syndrome; presence of nasal obstruction that prevents swab collection; participation in a clinical trial in the previous twelve months; any condition that, in the investigator's judgment, precludes participation for reasons of subject safety or data integrity; Cohort B - Having a negative result in the self-test with COVISTIX/COVIMARK during the selection visit; being immunocompromised or using an immunosuppressant; having chronic diseases such as diabetes, hypertension, asthma, chronic obstructive pulmonary disease, obesity; having a diagnosis of COVID-19 with symptoms of severe acute respiratory syndrome; presence of serious symptoms or symptoms that require hospital care; previous positive test for SARS-CoV-2 infection or confirmed diagnosis of COVID-19 more than 2 days; being hospitalized or requiring hospitalization; inability to maintain isolation for up to 9 days after signing the ICF, for conducting the self-test at home and collecting a nasal swab at home of RT-PCR for SARS-CoV-2 at the end of the study; inability to photograph cassettes with test results and send the images to the study center daily; presence of nasal obstruction that prevents swab collection; - participation in a clinical trial in the previous twelve months; any condition that, in the investigator’s judgment, precludes participation for reasons of subject safety or data integrity
研究者
相似试验
招募中
不适用
Performance evaluation of a sars-cov-2 rapid antigentest: test performance in the community in the netherlandsCOVID-19NL-OMON22075Amphia Hospital Breda1,000
已完成
不适用
Sensitivity of SARS-CoV-2 Rapid-Antigen-tests in vaccinated COVID-19 Patients: are negative test results misleading?Corona Virus Disease 19DRKS00027348Schwarzwald-Baar-Klinikum Villingen-Schwennigen234
进行中(未招募)
1 期
Detection and Characterization of Anti-SARS-CoV-2 Salivary Antibodies after COVID-19 Booster Vaccines – The CoVVacBoost Study - The CoVVacBoost StudyCovid (Coronavirus disease)- 19 immunisationMedDRA version: 23.1Level: PTClassification code 10084457Term: COVID-19 immunisationSystem Organ Class: 10042613 - Surgical and medical proceduresEUCTR2021-006172-16-ATMedical University of Graz1,200
已完成
不适用
Detection of SARS-CoV-2 using a rapid antigen test and PCR depending on symptoms and hospitalization status07.1DRKS00028072KH Labor GmbH149
进行中(未招募)
不适用
Clinical performance study of SARS-CoV-2 Antigen Self Test Nasal & SARS-CoV-2 Rapid Antigen Test 2.0 NasalCOVID-19DRKS00031144SD Biosensor INC452
