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Clinical Trial Summary

The purpose of this study is to validate the anti-müllerian hormone (AMH) cut-off established and validated in the APHRODITE study, for the determination of PCOM as part of the diagnosis of PCOS, using the Elecsys AMH Plus immunoassay.


Clinical Trial Description

The study participants will be women born July 1985-Dec 1987 in Northern Finland; the study partially links to the Northern Finland Birth Cohort 1986. Female subjects included in this cohort will be invited to participate in the study with the aim to enroll up to 1800 subjects. Each enrolled subject will have one study visit, where the clinical data required for assessing their PCOS status will be recorded, including a gynecological examination by transvaginal ultrasound to determine polycystic ovarian morphology (PCOM) status (antral follicle count and ovarian volume). Study subjects will also have blood drawn for serum collection, where hormonal parameters relevant for PCOS will be measured. The collected serum will also be used to measure the AMH levels using the Roche Elecsys AMH test. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05527353
Study type Observational
Source Oulu University Hospital
Contact Terhi T Piltonen, Professor
Phone +358 8 3153051
Email terhi.piltonen@oulu.fi
Status Recruiting
Phase
Start date May 13, 2020
Completion date December 31, 2022

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