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Clinical Trial Summary

The AMH^2 (Anti-Mullerian Hormone - At My Home) study is a head-to-head-to-head validation study aiming to evaluate the concordance of AMH levels found in blood collected via three different routes: collected at-home using the TAP II device, drawn through standard venipuncture techniques, and collected with the ADx card, another at-home collection device widely available on the market for commercial use.


Clinical Trial Description

Today, information regarding fertility potential is challenging to obtain for healthy women; clinically meaningful in-clinic testing is limited by physician availability and patient willingness to undergo testing in-clinic. Meanwhile, at-home hormonal bloodwork relies on the use of an ADx card, and is not widely accepted as clinically reliable by the medical community. The Sponsor is developing a comprehensive home fertility assessment to enable couples to proactively estimate and manage their fertility and family building options. Accurate and reliable at-home AMH testing is necessary to reach this goal. This study aims to validate the clinical excellence and medical accuracy of blood drawn via the TAP II device relative to a standard in-clinic venipuncture draw and other options available on the market to support emerging telemedicine care models. In doing so, the Sponsor may receive CLIA validation for the TAP II in AMH testing and commercialize a Lab Developed Test. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04784325
Study type Interventional
Source Turtle Health, Inc.
Contact
Status Completed
Phase N/A
Start date April 1, 2021
Completion date June 1, 2021

See also
  Status Clinical Trial Phase
Completed NCT05443698 - SELF-GYN1 (Sonograms Enable Looking Forward- Get Your iNformation 1 Trial) N/A
Withdrawn NCT05509322 - Care Expansion Across Remote Environments - Sub-Study of the SELF-GYN1 Trial N/A
Completed NCT04687189 - Sonograms Enable Looking Forward - Home Examinations Led by Providers Validation Study N/A