COVID-19 Vaccine and Ovarian Reserve
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The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. |
ClinicalTrials.gov Identifier: NCT04748172 |
Recruitment Status :
Active, not recruiting
First Posted : February 10, 2021
Last Update Posted : April 8, 2022
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Condition or disease | Intervention/treatment |
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Fertility Issues Vaccine Adverse Reaction | Biological: SARS-CoV-2 virus vaccines Diagnostic Test: AMH sampling Diagnostic Test: anti Covid-19 antibody levels (Serology) |

Study Type : | Observational |
Estimated Enrollment : | 200 participants |
Observational Model: | Case-Control |
Time Perspective: | Prospective |
Official Title: | The Effect of COVID -19 mRNA Vaccine on Ovarian Reserve |
Actual Study Start Date : | February 1, 2021 |
Estimated Primary Completion Date : | February 2024 |
Estimated Study Completion Date : | February 2024 |

Group/Cohort | Intervention/treatment |
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Study Group: Women who are planning to be vaccinated
Women that are planning to be vaccinated, before receiving the first shot of the vaccine
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Biological: SARS-CoV-2 virus vaccines
mRNA SARS-CoV-2 virus vaccines ( By Pfizer or Moderna) Diagnostic Test: AMH sampling Blood sample for AMH on recruitment and after three months Diagnostic Test: anti Covid-19 antibody levels (Serology) Blood sample for IgG against S1 protein after three months |
- Delta in AMH levels [ Time Frame: From first vaccination until the second AMH sampling - after three month ]AMA levels on recruitment minos AMH levels after three months
Biospecimen Retention: Samples Without DNA

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 11 Years to 42 Years (Child, Adult) |
Sexes Eligible for Study: | Female |
Gender Based Eligibility: | Yes |
Gender Eligibility Description: | Women in reproductive age |
Accepts Healthy Volunteers: | Yes |
Sampling Method: | Non-Probability Sample |
Inclusion Criteria:
- Age 11-42
- No previous exposure to Covid-19 vaccine (first or second dose)
- No known past Covid-19 infection
Exclusion Criteria:
- Premature ovarian failure
- Pregnancy
- Fertility treatment
- Past Covid-19 infection

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04748172
Israel | |
Sheba Medical Center | |
Ramat-Gan, Israel, 56506 |
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
Responsible Party: | Dr. Aya Mohr-Sasson, Principal Investigator, Sheba Medical Center |
ClinicalTrials.gov Identifier: | NCT04748172 |
Other Study ID Numbers: |
8121-21-SMC |
First Posted: | February 10, 2021 Key Record Dates |
Last Update Posted: | April 8, 2022 |
Last Verified: | April 2022 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Undecided |
Plan Description: | On request |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
Ovarian reserve Corona-19 virus SARS-CoV-2 |
Infertility Antibodies Immunologic Factors Physiological Effects of Drugs |