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OpenTrials
Completed

NCT Number: NCT04832828

Sensitivity and Specificity of the Roth Test in Patients With COVID-19 Positive

The presence of the described silent hypoxia in subjects diagnosed with COVID19 highlights the need for valid tools to assess respiratory capacity. The Roth test has been associated with acceptable sensitivity and specificity criteria in patients with previous respiratory pathology; however, its validity in this type of patient has not been proven.

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Key information

Age range

12 year–99 year

Sex eligibility

All sexes

Study type

Observational

Primary location

CS Entrevías

Madrid, 28053, Spain

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • having been diagnosed as COVID-19 positive and with symptoms compatible with Sars-Cov-2 infection in the last 7 days prior to assessment,
  • having an understanding of Spanish,
  • and having no history of respiratory pathology prior to the current infection.

Treatment and study plan

Roth´s Test

Diagnostic Test

Subjets must count from 1 to 30 in their languages, and health professional will count seconds that last in take breath during the count.

Primary outcomes

  1. Oxygen Saturation

    Time frame: 12 weeks

    The pulseoximeter percentage value

Secondary outcomes

  1. Roth´s test

    Time frame: 12 weeks

    The level described in the test

Sponsors and collaborators

Lead sponsor

Universidad Autonoma de Madrid

Other

Registry information

Important dates

Study start
2020
Primary completion
2020
Study completion
2020
First posted
Apr 6, 2021
Registry last updated
Apr 6, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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