ClinicalTrials.Veeva

Menu

Evaluating a New Gonadotoxic Risk Stratification System

University of Colorado Denver (CU Denver) logo

University of Colorado Denver (CU Denver)

Status

Withdrawn

Conditions

Cancer

Study type

Observational

Funder types

Other

Identifiers

NCT05052632
21-3084

Details and patient eligibility

About

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.

Sex

Female

Ages

8 to 39 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Female patients ages 8 - 39 years of age

  • Seen in CHCO or AMC outpatient clinics for any of the following reasons:

    • At risk for fertility problems (Z91.89)
    • Encounter for fertility preservation counseling (Z31.62)
    • Primary ovarian insufficiency
    • Premature ovarian failure/premature menopause
    • Diminished ovarian reserve
  • 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:

    • Any type of cancer/malignancy
    • Rheumatoid arthritis
    • Systemic lupus erythematosus
    • Aplastic anemia
    • Fanconi anemia
    • Diamond-Blackfan syndrome
    • Hurler syndrome
    • Other autoimmune conditions

Exclusion criteria

  • Disorders of sexual development (i.e., gonadal dysgenesis, Turner syndrome/mosaicism, etc.)
  • History of bilateral oophorectomy
  • Transgender patients not receiving chemotherapy; radiation; or surgery to the reproductive organs for malignancy
  • Inability to consent/assent

Trial contacts and locations

1

Loading...

Central trial contact

Hadley Kelly, MPH

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems