Semen Analysis Parameters Following Pfizer's COVID-19 Vaccine

Sponsor
Sheba Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT04778033
Collaborator
(none)
75
1
2.7
28.2

Study Details

Study Description

Brief Summary

In this study the investigators will explore the effect of the BNT162b2 COVID-19 Vaccine on semen analysis parameters among 75 fertile men. Fertile men will be regarded as such if they previously successfully impregnated their partners without the use of artificial reproductive technology, or men who previously had a normal sperm analysis exam by WHO criteria (2010). Those recruited will supply a single sperm sample 1-2 months following the second dose of the vaccination. In addition, the participants will fill a brief questionnaire with information regarding their medical and reproductive history. The investigators will examine the macroscopic and microscopic properties of the semen samples and compare them to the WHO semen analysis reference range in an attempt to ascertain whether the vaccine influences sperm parameters.

Condition or Disease Intervention/Treatment Phase
  • Other: Sperm collection

Detailed Description

The 2019 novel coronavirus disease (COVID-19) is a highly infectious respiratory tract disease which was first reported in Wuhan, Hubei Province, China in Dec 2019, but has since spread globally. By march 2020 it was declared by WHO as a public health emergency pandemic and has thus far affected tens of millions worldwide. The implications of COVID 19 infection on male fertility were examined in a previous study, which found decreased sperm concentration in recovering patients compared with controls.

The newly available mRNA COVID 19 vaccine by Pfizer was recently evaluated in a large multicenter placebo controlled RCT. The vaccine is comprised of BNT162b2, a lipid nanoparticle formulated nucleoside-modified RNA (modRNA) encoding the SARS-CoV2 full length spike protein, modified by two Proline mutations. The two 20 µg doses were shown to elicit high SARS-COV2 neutralizing antibody titers alongside high antigen specific CD8+ and Th1 type CD4+ T cell response. It was subsequently shown to be 95% effective in preventing COVID-19 infection a week following the second dose with a favorable safety profile in a 2-month median following up time.

Unfounded claims in the popular media linked a possible correlation between the COVID-19 vaccine and potential female\male infertility. Currently. there is no information in the medical literature which examined semen analysis parameters following the COVD-19 vaccine.

In this study the investigators will explore the effect of the BNT162b2 COVID-19 Vaccine on semen analysis parameters among 75 fertile men. Fertile men will be regarded as such if they previously successfully impregnated their partners without the use of artificial reproductive technology, or men who previously had a normal sperm analysis exam by WHO criteria (2010). Those recruited will supply a single sperm sample 1-2 months following the second dose of the vaccination. In addition, the participants will fill a brief questionnaire with information regarding their medical and reproductive history. The investigators will examine the macroscopic and microscopic properties of the semen samples and compare them to the WHO semen analysis reference range in an attempt to ascertain whether the vaccine influences sperm parameters.

Study Design

Study Type:
Observational
Anticipated Enrollment :
75 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
The Effect of BNT162b2 mRNA COVID-19 Vaccine on Semen Analysis Parameters Among 75 Fertile Men
Actual Study Start Date :
Feb 9, 2021
Anticipated Primary Completion Date :
Apr 10, 2021
Anticipated Study Completion Date :
May 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Vaccinated Men

Fertile men who were vaccinated with the BNT162b2 COVID-19 Vaccine

Other: Sperm collection
Those recruited will supply a single sperm sample 1-2 months following the second dose of the vaccination. The sample will be analyzed for macroscopic and microscopic features in the IVF laboratory and will be discarded immediately afterwards.

Outcome Measures

Primary Outcome Measures

  1. Sperm Concentration (10^6/ml) [1-2 months after the second COVID-19 vaccine]

    Semen concentration (10^6/ml)

  2. Sperm Motility (%) [1-2 months after the second COVID-19 vaccine]

    Sperm percentage with proper forward progression

  3. White Blood Cells (10^6/ml) in Semen [1-2 months after the second COVID-19 vaccine]

    Amount of white blood cells (10^6/ml) in semen

  4. Sperm Morphology (%) [1-2 months after the second COVID-19 vaccine]

    Sperm morphology (%)

  5. Sperm Vitality (%) [1-2 months after the second COVID-19 vaccine]

    Sperm vitality (%)

  6. Semen Liquefaction (normal/abnormal) [1-2 months after the second COVID-19 vaccine]

    Macroscopic appearance - Semen liquefaction appearance

  7. Semen Viscosity (normal/abnormal) [1-2 months after the second COVID-19 vaccine]

    Macroscopic appearance - Semen viscosity appearance

  8. Semen Color [1-2 months after the second COVID-19 vaccine]

    Macroscopic appearance - Semen color appearance

  9. Semen PH [1-2 months after the second COVID-19 vaccine]

    Semen PH

  10. Semen Volume (ml) [1-2 months after the second COVID-19 vaccine]

    Semen Volume (ml)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 45 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Previously impregnated their partner without the use of assisted reproduce technology, or previously had a normal sperm analysis exam by WHO 2010 criteria.

  • 1-2 months following the second dose of BNT162b2 COVID-19 Vaccine.

Exclusion Criteria:
  • Known abnormal semen parameters.

  • Age above 45.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sheba medical center Ramat Gan Israel

Sponsors and Collaborators

  • Sheba Medical Center

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr. Jigal Haas MD, Senior Gynecologist and Obstetrician, Sheba Medical Center
ClinicalTrials.gov Identifier:
NCT04778033
Other Study ID Numbers:
  • SHEBA - 21 - 8079- JH - CTIL
First Posted:
Mar 2, 2021
Last Update Posted:
Mar 2, 2021
Last Verified:
Feb 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 2, 2021