Blood Sample Markers of Reproductive Hormones in Assessing Ovarian Reserve in Younger Patients With Newly Diagnosed Lymphomas
Completed
Conditions studied: Anaplastic Large Cell Lymphoma, Burkitt Lymphoma, Diffuse Large B-Cell Lymphoma, Hodgkin Lymphoma, Lymphoma
In brief
This clinical trial studies blood sample markers of reproductive hormones in assessing ovarian reserve in younger patients with newly diagnosed lymphomas. Studying samples of blood from patients with cancer in the laboratory may help measure the effect of curative therapy for lymphoma on ovarian failure.
Key facts
- Study ID
- NCT01793233
- Run by
- Children's Oncology Group
- People needed
- 203
- Starts
- 2013-06-17
- Expected to finish
- 2024-06-30
- Last updated by the study team
- 2024-08-26
Who can join
Age: any, up to 29. Sex: female. Healthy volunteers: not accepted.
You may qualify if…
- Patients must have had first menses >= 6 months prior to enrollment
- Patients must be newly diagnosed with lymphoma; this includes but is not limited to Hodgkin lymphoma, Burkitts lymphoma, diffuse large B cell lymphoma, and anaplastic large cell lymphoma
- Planned cancer treatment must include an alkylating agent: i.e. procarbazine, cyclophosphamide, ifosphamide; planned cancer treatment must be less than one year
- Patients with any performance status are eligible for enrollment
- Patients may take hormone medications excluding gonadotropin-releasing hormone (GnRH) analogues
- All patients and/or their parents or legal guardians must sign a written informed consent
- All institutional, Food and Drug Administration (FDA), and National Cancer Institute (NCI) requirements for human studies must be met
You may not qualify if…
- Patients who have previously received chemotherapy other than steroids and intrathecal chemotherapy are not eligible
- Patients who have a secondary malignancy are not eligible
- Patients with known history of ovarian disease: e.g. Turner syndrome or polycystic ovarian syndrome are not eligible
- Patients in whom planned therapy includes: removal or uterus or ovary(ies), pelvic irradiation, cranial irradiation or hematopoietic stem cell transplantation are not eligible
- Patients who previously have had their uterus or ovary(ies) removed are not eligible
- Patients who have received gonadotropin release hormone agonist or antagonist (e.g. Lupron) prior to study entry are not eligible
- Patients who are pregnant or breast feeding are not eligible
- Patients who have undergone or are planning to undergo ovarian tissue, oocyte or embryo cryopreservation prior to treatment are not eligible
Where it is running
- Arkansas Children's Hospital — Little Rock, Arkansas, United States
- Kaiser Permanente Downey Medical Center — Downey, California, United States
- City of Hope Comprehensive Cancer Center — Duarte, California, United States
- Loma Linda University Medical Center — Loma Linda, California, United States
- Miller Children's and Women's Hospital Long Beach — Long Beach, California, United States
- Children's Hospital of Orange County — Orange, California, United States
- Lucile Packard Children's Hospital Stanford University — Palo Alto, California, United States
- Rady Children's Hospital - San Diego — San Diego, California, United States
- UCSF Medical Center-Parnassus — San Francisco, California, United States
- UCSF Medical Center-Mission Bay — San Francisco, California, United States
- Connecticut Children's Medical Center — Hartford, Connecticut, United States
- Alfred I duPont Hospital for Children — Wilmington, Delaware, United States
- Children's National Medical Center — Washington D.C., District of Columbia, United States
- Golisano Children's Hospital of Southwest Florida — Fort Myers, Florida, United States
- Memorial Regional Hospital/Joe DiMaggio Children's Hospital — Hollywood, Florida, United States
- Nemours Children's Clinic-Jacksonville — Jacksonville, Florida, United States
- Miami Cancer Institute — Miami, Florida, United States
- Nemours Children's Hospital — Orlando, Florida, United States
- Nemours Children's Clinic - Pensacola — Pensacola, Florida, United States
- Johns Hopkins All Children's Hospital — St. Petersburg, Florida, United States
- Tampa General Hospital — Tampa, Florida, United States
- Saint Joseph's Hospital/Children's Hospital-Tampa — Tampa, Florida, United States
- Saint Mary's Hospital — West Palm Beach, Florida, United States
- Children's Healthcare of Atlanta - Egleston — Atlanta, Georgia, United States
- Children's Hospital of Alabama — Birmingham, Alabama, United States
Full record on ClinicalTrials.gov
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