FemaSeed LOCAL Artificial Insemination Trial

  • End date
    Jul 19, 2022
  • participants needed
  • sponsor
    Femasys Inc.
Updated on 19 September 2021
intrauterine insemination


The objectives of the trial are to evaluate the safety and effectiveness of the FemaSeed Localized Directional Insemination for artificial insemination.

Condition Female Genital Diseases, Infertility, sterility, unable to conceive
Treatment FemaSeed Localized Directional Insemination
Clinical Study IdentifierNCT04968847
SponsorFemasys Inc.
Last Modified on19 September 2021


Yes No Not Sure

Inclusion Criteria

Female, 19-40 years of age, and infertile
Meets qualifications for standard intrauterine insemination procedure
At least one patent fallopian tube with no evidence of hydrosalpinx

Exclusion Criteria

Greater than three prior intrauterine insemination (IUI) cycles or any prior assisted reproduction procedure (e.g. IVF)
Current or recent pelvic infection
Prior ectopic pregnancy or tubal surgery other than salpingectomy
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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