COVINF: COVID-19 Infection and Reproductive Health in Infertile Women

Sponsor
University of Palermo (Other)
Overall Status
Recruiting
CT.gov ID
NCT05435430
Collaborator
(none)
150
1
18
8.3

Study Details

Study Description

Brief Summary

An increased number of women has been infected by COVID-19 in the last 2 years SARS-CoV-2 infection could have a role in potential disturbances on hormon levels and human fertility Has not completely demonstrated COVID-19 effects on female reproductive function and further research can be undertaken.

The proposed multicenter study will be simple and rapid, and attractive for the scientific community.

Condition or Disease Intervention/Treatment Phase
  • Other: PERSPECTIVE, MULTICENTRIC and observational

Detailed Description

COVID-19 virus is classified as a respiratory disease that drastically changed our daily life and perspective (1) can be mainly transmitted via respiratory droplets, however, there are recently published reports suggested its ability to transmit via sexual intercourse, assisted reproductive technology (ART) treatments, pregnancy, and nursing. ART specialists should be precautious, carefully following the situation while contributing by sharing novel evidence to counsel our patients (2).

However, there are no comprehensive reviews to explore the association between COVID-19 and female fertility comprehensively.Its of major importance to provide in-depth research explaining the underlying mechanism of SARS-CoV-2 infection and its impact on human reproductive organs and fertility (3).

Ovarian reserve is a key determinant of female fertility. In this study we observe the potential effects of SARS-CoV-2 infection on the principal indicators of ovarian reserve function as anti-Müllerian hormone (AMH); basal follicle-stimulating hormone (FSH), basal luteinising hormone (LH) basal oestradiol (E2) antral follicle count (AFC).

Questions regarding the potential risks of sexual transmission during intercourse and/or application of ART, vertical transmission (throughout pregnancy, delivery, and breastfeeding), the health of pregnant and postpartum women, and fetal or postnatal health problems of neonates/children remain largely unanswered (4,5).

Study Design

Study Type:
Observational
Anticipated Enrollment :
150 participants
Observational Model:
Other
Time Perspective:
Prospective
Official Title:
Post-COVID-19 Infection and Reproductive Health in Women Undergoing I.V.F. Treatment
Anticipated Study Start Date :
Sep 1, 2022
Anticipated Primary Completion Date :
Sep 30, 2023
Anticipated Study Completion Date :
Mar 1, 2024

Arms and Interventions

Arm Intervention/Treatment
women with previously SARS-COV2 infection.

2 group from 2 IVF CENTER with egual criteria : INCLUSION CRITERIA: Women 24-43 years of age Previous history of COVID-19 infection INFERTILITY DIAGNOSIS ESCLUSION CRITERIA: women with current symptoms of COVID-19 infection Positive for HIV or the presence of active viral hepatitis Previosuly ovarian cancer, removal of ovaries or gonadotoxic treatments

Other: PERSPECTIVE, MULTICENTRIC and observational
we will enroll women with 25-45ys old and previously SARS-COV2 infection. first outcome to be investigate the impact of SARS-COV2 infection on female reproductive health and the main clinical-laboratory parameters (FSH, LH, AMH) relating to women with procreative research, in a path of medically procreation assisted programm and on any quantitative variations, duration and periodicity of the menstrual cycle after Covid infection compared to the pre-infection period.

Outcome Measures

Primary Outcome Measures

  1. Main outcome [18 months]

    To investigate how the SARS-COV2 infection affects the female reproductive health and the main clinical-laboratory parameters (FSH, LH, AMH) relating to women with procreative research in a path of medically assisted procreation and any quantitative variations, duration and periodicity of the menstrual cycle after Covid infection.19 compared to the pre-infection period.

Secondary Outcome Measures

  1. secondary outcomes [18 months]

    Quantification of the number of good quality oocytes (MII) . Number of embryos on day 3 (Morula) or day 5 (blastocyst) of development transferred to the patients. Thickness of the endometrium at the time of embryo transfer (ET).

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years to 45 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

Women 24-43 years of age Previous history of COVID-19 infection INFERTILITY DIAGNOSIS

Exclusion Criteria:

Women with current symptoms of COVID-19 infection Positive for HIV or the presence of active viral hepatitis Previosuly ovarian cancer, removal of ovaries or gonadotoxic treatments

Contacts and Locations

Locations

Site City State Country Postal Code
1 Aoor Villa Sofia Cervello Palermo Italy 90100

Sponsors and Collaborators

  • University of Palermo

Investigators

  • Principal Investigator: Giuseppe Gullo, MD.Ph.D, AOOR VILLA SOFIA CERVELLO

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
GIUSEPPE GULLO, GIUSEPPE GULLO MD. Ph.D, University of Palermo
ClinicalTrials.gov Identifier:
NCT05435430
Other Study ID Numbers:
  • AOOR VILLA SOFIA CERVELLO
First Posted:
Jun 28, 2022
Last Update Posted:
Jun 28, 2022
Last Verified:
Jun 1, 2022
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
Keywords provided by GIUSEPPE GULLO, GIUSEPPE GULLO MD. Ph.D, University of Palermo
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 28, 2022