Detection of COVID-19 (SARS-CoV-2) in the Semen of COVID+ Patients (Positive RT-PCR on a Nasopharyngeal Swab)

  • STATUS
    Recruiting
  • participants needed
    100
  • sponsor
    GCS Ramsay Santé pour l’Enseignement et la Recherche
Updated on 19 February 2024
covid-19
SARS
nasopharyngeal swab
acute respiratory syndrome (sars)

Summary

The objective of this study is to look for the presence of SARS-CoV-2 in the semen of patients diagnosed with COVID+ based on RT-PCR analysis of nasopharyngeal swabs.

Description

This is a prospective monocentric, open-label, prospective study of male patients with CoV-2-SARS.

Details
Condition COVID
Age 18-65 years
Treatment diagnostic
Clinical Study IdentifierNCT04460534
SponsorGCS Ramsay Santé pour l’Enseignement et la Recherche
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

Male patient between the ages of 18 and 65 who has read and signed the consent form for participation in the study
Outpatient or inpatient without signs of respiratory severity, likely to be mobile
Patient whose medical condition warrants screening for COVID-19 by nasopharyngeal swab

Exclusion Criteria

Patient under protective custody, guardianship or trusteeship
Patient not affiliated to the French social security system
Inability to provide the subject with informed information and/or written informed consent: dementia, psychosis, consciousness disorders, non-French speaking patient
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Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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