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Retrospective Study on the Use, Efficiency, and Safety of the At-home Mosie Kit

NCT04646291 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 350

Last updated 2021-06-24

Study results available
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Summary

This study examines the experience of people who have selected to use the at-home insemination Mosie Kit to understand the user's experience, the perceived safety and the efficiency. People who have recently purchased and voluntarily selected to use the Mosie Kit will be invited to complete a one-time online anonymous survey. The results of the survey will be analyzed to understand their experiences.

Conditions

Interventions

DEVICE

Insemination with the Mosie Baby Kit

The participant will have performed at least one cycle of insemination using the Mosie Baby Kit.

Sponsors & Collaborators

  • Mosie Baby

    lead INDUSTRY

Principal Investigators

  • Karina Loyo, PhD MBA CCDM · Independent Researcher

Eligibility

Sex
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-08-05
Primary Completion
2020-08-31
Completion
2020-09-01
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04646291 on ClinicalTrials.gov