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Completed Not applicable Interventional Accepts healthy volunteers

FemaSeed LOCAL Artificial Insemination Trial

ClinicalTrials.gov ID: NCT04968847

Public ClinicalTrials.gov record NCT04968847. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 3:17 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

LOCAL: Prospective Multi-Center LOCALized Directional Insemination Trial for Artificial Insemination

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Brief Summary: The objectives of the trial are to evaluate the safety and effectiveness of the FemaSeed Localized Directional Insemination for artificial insemination, now known as the FemaSeed Intratubal Insemination since FDA Cleared under K231730 in September 2023.

Study identification

NCT ID
NCT04968847
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Femasys Inc.
Industry
Enrollment
314 participants

Conditions and interventions

Eligibility (public fields only)

Age range
19 Years to 40 Years
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 15, 2021 (Actual)
Primary completion
Dec 31, 2023 (Actual)
Completion
Apr 30, 2024 (Actual)
Last update posted
Nov 8, 2024

2021 – 2024

United States locations

U.S. sites
18
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Elite IVF, PLLC Mobile Alabama 36608 —
Reproductive Associates of Delaware (RAD Fertility) Newark Delaware 19713 —
Women's Medical Research Group, LLC Clearwater Florida 33759 —
Rosemark Women Care Specialists Idaho Falls Idaho 83404 —
Saginaw Valley Medical Research Group Saginaw Michigan 48604 —
The Fertility Center of Las Vegas Las Vegas Nevada 89117 —
Red Rock Fertility Center Las Vegas Nevada 89148 —
Reach Fertility Charlotte North Carolina 28207 —
Carolina Conceptions Raleigh North Carolina 27607 —
Institute for Reproductive Health Cincinnati Ohio 45209 —
University of Cincinnati Physicians Cincinnati Ohio 45229 —
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104 —
Main Line Fertility Bryn Mawr Pennsylvania 19010 —
University of Pennsylvania (Pennsylvania Fertility Care) Philadelphia Pennsylvania 19104 —
LinQ Research Sugar Land Texas 77479 —
Center of Reproductive Medicine Webster Texas 77598 —
Utah Center for Reproductive Medicine Salt Lake City Utah 84108 —
University of Wisconsin, Generations Fertility Care Middleton Wisconsin 53562 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04968847, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 8, 2024 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04968847 live on ClinicalTrials.gov.

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