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The primary objective of this study is to assess if there is an association between a newly described gonadotoxic risk stratification system and post-treatment ovarian reserve as determined by FSH and AMH.
Full description
The Investigator will test the amount of agreement between the two ordinal variables using a kappa statistic at each time point in the first two years of follow up. The Investigator will perform ordinal logistic regression accounting for repeated measures data for participants who are not using contraception. The Investigator will assess participant characteristics to see if the Investigator need to adjust for other covariates including age, race, ethnicity and body mass index (BMI).
Since contraception can mask an elevated FSH surge from gonadal failure, the Investigator will perform a similar model for participants on contraception using AMH only.
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Inclusion criteria
Female patients ages 8 - 39 years of age
Seen in CHCO or AMC outpatient clinics for any of the following reasons:
At least 12 months post-completion of chemotherapy and/or radiation
History of a fertility-threatening diagnosis receiving chemotherapy; radiation; or surgery to the reproductive organs for malignancy, including but not limited to:
Exclusion criteria
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Central trial contact
Hadley Kelly, MPH
Data sourced from clinicaltrials.gov
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