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Pilot Study to Detect SARS-CoV-2 Virus in Sperm (COVSPERM)

T

Toulouse University Hospital

Status

Unknown

Conditions

Covid19

Treatments

Biological: Sample

Study type

Interventional

Funder types

Other

Identifiers

NCT04584593
2020-A01610-39 (Other Identifier)
RC31/20/0202

Details and patient eligibility

About

This is a prospective study involving 50 patients, with acute SARS-CoV-2 infection and a positive RNA detection. Men will give semen, saliva, urine and blood specimens following RT-PCR diagnosis and 15, 30, 60 and 90 days after. SARS-CoV-2 RNA will be detected in seminal plasma, native semen cells and processed spermatozoa.

The purpose of this study is to seek the presence of SARS-CoV-2 in semen, to determine its localization and infectiousness and to assess the efficiency of spermatozoa processing methods to obtain virus free spermatozoa.

Full description

Since the end of 2019, an epidemic of SARS-CoV-2 infections (COVID-19) began in China and is now a global pandemic affecting more than 3 millions of people. Droplets and close contact are the most common routes of transmission of SARS-CoV-2 and aerosol transmission may be another route. Researchers have detected SARS-CoV-2 in samples of respiratory tract, saliva, stool, gastrointestinal tract, urine, tears and conjunctival secretions of COVID-19 patients.

Vertical transmission from mother to infant has been suspected, but not confirmed to date. Information about localization of SARS-CoV-2 in the genital tract or shedding is poorly documented and the results of these studies were discrepant. One of two studies have reported SARS-CoV-2 RNA in semen from six infected patients. However, there is no data on the duration of the seminal excretion of the virus, its viral load and infectiousness and on its localization in semen compartments (cells, seminal plasma, spermatozoa).

The purpose of this study is to seek the presence of SARS-CoV-2 in semen, to determine its localization and infectiousness and to assess the efficiency of spermatozoa processing methods to obtain virus free spermatozoa.

This is a prospective study involving 50 patients, with acute SARS-CoV-2 infection and a positive RNA detection. Men will give semen, saliva, urine and blood specimens following RT-PCR diagnosis and 15, 30, 60 and 90 days after. SARS-CoV-2 RNA will be detected in seminal plasma, native semen cells and processed spermatozoa.

Enrollment

50 estimated patients

Sex

Male

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patient aged 18 to 50, male.
  • Patient in acute phase of infection with SARS-CoV-2 and whose RT-PCR shows the viral genome in the nasopharyngeal or salivary sample or in any other sample.
  • Patient who can come to the laboratory for samples
  • Patient having given his free and informed consent and having signed the consent
  • Patient affiliated to a social security scheme or equivalent

Exclusion criteria

  • Patient having previously consulted for male infertility or having previously carried out a semen examination which was abnormal (WHO standard)
  • Patient with ejaculation disorder or unable to take a semen sample or with an abnormal semen volume (<1.5 mL).
  • Patient who would present serious clinical signs that would not allow him to travel to the investigating center to take samples.
  • Patient under a protection regime for adults (including guardianship, curatorship or safeguard of justice.

Trial design

Primary purpose

Other

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

50 participants in 1 patient group

SARV-Cov
Other group
Description:
Men will give semen, saliva, urine and blood specimens
Treatment:
Biological: Sample

Trial contacts and locations

1

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Central trial contact

Louis BUJAN, PR

Data sourced from clinicaltrials.gov

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