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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04599959
Other study ID # 0352-2150
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 26, 2020
Est. completion date January 20, 2021

Study information

Verified date July 2021
Source Boehringer Ingelheim
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main objective of the tests is to establish saliva collection with Salivette® Cortisol.


Recruitment information / eligibility

Status Completed
Enrollment 151
Est. completion date January 20, 2021
Est. primary completion date January 20, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Informed consent form signed and dated before any samples have been taken. 2. Suspected or confirmed SARS-CoV-2 infection by PCR within the past five days. 3. Male and/or female patients aged 18 years and over.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Sampling of SARS-CoV-2 RNA from nasopharyngeal swab specimen or saliva collected via Salivette Cortisol
Kylt® for detection/confirmation of SARS-CoV-2 cobas® SARS-CoV-2 (PCR) test TaqPath™ COVID-19 CE-IVD RT-PCR kit

Locations

Country Name City State
Mexico Instituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas Mexico

Sponsors (1)

Lead Sponsor Collaborator
Boehringer Ingelheim

Country where clinical trial is conducted

Mexico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Participants Testing Positive or Negative for SARS-CoV-2 Virus From Swab and Saliva Samples - Processed in Mexico Number of participants testing positive or negative for SARS-CoV-2 virus from sample collected via swab versus saliva sample collected from Salivette® Cortisol, which samples were processed in Mexico. At baseline (the test day), up to one day.
Primary Percentage of Participants Testing True Positive or True Negative for SARS-CoV-2 Virus From Swab and Saliva Samples - Processed in Germany Percentage of participants testing true positive or true negative for SARS-CoV-2 virus from Swab and Saliva samples being processed in Germany was reported. The swab sample was used as the reference. Among participants who were tested positive from swab samples, those who were tested positive from saliva samples were classified as "true positive". Among participants tested negative from swab samples, those who were tested negative from saliva samples were then classified as "true negative". At baseline (the test day), up to one day.
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