About this trial
The purpose of this study is to have a better understanding of the normal blood levels of AMH in females from 0-18 years of age and how the blood AMH levels correspond to a female's reproductive development.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Pre- and post-pubertal females
Ages 0-18 years old
Tanner Stage I- V
Undergoing routine outpatient surgical procedure
Disqualifiers
Previous diagnosis of an illness associated with premature ovarian failure (Turner's syndrome, Fragile X permutation carrier) or endocrine disorder associated with irregular menstrual cycles (Cushing's disease, poorly-controlled Thyroid disease, hyperprolactinemia, polycystic ovary syndrome, and congenital adrenal hyperplasia) or insulin-dependent diabetes mellitus or autoimmune disorders
Previous diagnosis of any malignancy or any history of systemic/local chemotherapy, radiation therapy, or stem-cell transplant.
Previous surgical excision of one ovary or both ovaries
Pregnant females
Trial design
Single group
Treatments tested in this trial
Blood sample collection
Diagnostic testBlood samples are collected for diagnostically assessing how the blood AMH levels correspond to a female's reproductive development
Treatment groups
Trial outcomes
Primary outcomes
Anti-mullerian Hormone Levels in Healthy Females
The primary outcome measure is to get a better understanding of the normal AMH levels in children (girls aged 0-18 years) in order to better assess a girl's risk of not being able to have children if she is a cancer patient, and in offering her and her family options to increase the chances of having her own children
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
Erin Rowell
Lead sponsor
Ann & Robert H Lurie Children's Hospital of Chicago
Sponsor institution
Ann & Robert H Lurie Children's Hospital of Chicago
Collaborator