Ovarian Cancer Clinical Trial
Ovarian Reserve After Cancer: Longitudinal Effects
Summary
Women of reproductive age who will receive treatment for cancer that includes chemotherapy may participate in a study measuring ovarian function over time. Eligible women are asked to complete a questionnaire, a menstrual diary, a brief physical examination, an ultrasound, and a blood test before, during and after cancer treatment.
Full Description
A total of 7 study visits will be completed at 3 month intervals including 1 visit prior to treatment, and at least 2 visits after completion of treatment. Duration of study participation is 18-30 months, depending on length of treatment.
Review and Documentation of Cancer Therapy will be abstracted from the clinical oncology chart by the oncology offices caring for the patient. Treatment will be summarized in terms of chemotherapeutic type, duration and cumulative dose; total radiation dose and location; history and type of bone marrow transplantation; and any surgery. Any attempts at fertility preservation or use of gonadotropin releasing hormone agonist treatment during cancer therapy will be captured as well.
Eligibility Criteria
Inclusion Criteria for exposed population:
Postmenarchal females to be treated with chemotherapy
between the ages of 11-35 years,
with a uterus and at least one ovary
Inclusion Criteria for unexposed population:
healthy postmenarchal females
no prior or planned exposure to chemotherapy
between the ages of 11-35,
with a uterus and at least one ovary
regular menstrual cycles (21-35 days)
Exclusion criteria for all subjects:
positive pregnancy test at enrollment
lactation within the previous 1 month,
previous treatment with chemotherapy or radiation therapy with the exception of radioactive iodine for thyroid cancer.
previous diagnosis of an illness associated with premature ovarian failure (Turner's syndrome, Fragile X permutation carrier)
endocrine disorder associated with irregular menstrual cycles (Cushing's disease, Thyroid disease, hyper-prolactinemia, congenital adrenal hyperplasia).
Additional exclusions for the unexposed population:
a history of infertility, defined as at least 12 months of unprotected intercourse without conception
polycystic ovary syndrome (PCOS)
Check Your Eligibility
Let’s see if you might be eligible for this study.
What is your age and gender ?
There is 1 Location for this study
Philadelphia Pennsylvania, 19104, United States
How clear is this clinincal trial information?
Please confirm you are a US based health care provider:
Yes, I am a health care Provider No, I am not a health care providerSign Up Now.
Take Control of Your Disease Journey.
Sign up now for expert patient guides, personalized treatment options, and cutting-edge insights that can help you push for the best care plan.