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Clinical Trial Summary

To assess whether the presence of Cytomegalovirus (CMV) Immunoglobulin G (IGG) antibodies in semen is a reliable predictor of male subfertility or infertility.


Clinical Trial Description

Prospective cohort study performed in the artificial reproductive technology (ART) unit. The study will evaluate semen and serum samples from the following groups: 1. Presumably fertile male patients going through ART treatment (for preimplantation genetic testing (PGT) or female indications). 2. Subfertile/infertile male patients with abnormal semen analysis. 3. Male patients suffering from unexplained infertility. All samples will be collected on the day of ovum retrieval procedure, and the semen samples will be evaluated only after completing the fertilization process. The samples will be tested for CMV IGG antibodies and testosterone levels in semen and serum. In addition, anti-sperm antibodies will be measured in the serum. The ratio between CMV IGG antibodies in semen and serum will be calculated, and will be compared with presence of hormone profile, semen analysis parameters and ART parameters. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05302856
Study type Interventional
Source Hadassah Medical Organization
Contact Chana Adler Lazarovits, MD
Phone 00 972 50 8779068
Email chanaa@hadassah.org.il
Status Recruiting
Phase N/A
Start date March 2, 2022
Completion date March 2023

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