Research Studies and Clinical Trials Search
Results
Turner Syndrome (TS), The Brain, and Hormone Replacement Therapy (HRT): A study evaluating brain structure and function in adolescents and young adults with Turner syndrome who use hormone replacement therapy as compared to those without Turner syndrome
This study is for teen girls and young adult women: • Ages 14-21 years • With and without Turner syndrome...
This study is for teen girls and young adult women: • Ages 14-21 years • With and without Turner syndrome The goal of this study is to understand how hormones from the ovaries affect brain development. Every person is unique and the ovaries of some teens and young adults do not produce enough hormones. What researchers learn from this study could help the care team find better treatments for teens and young adults whose ovaries do not make enough hormones.
Turner Syndrome (TS): A study on progesterone supplementation to look at bleeding patterns
This study is for teen girls and young adult women: - With Turner Syndrome - Ages 12-20 years old - Prescribed hormone replacement therapy (HRT)...
This study is for teen girls and young adult women: - With Turner Syndrome - Ages 12-20 years old - Prescribed hormone replacement therapy (HRT) This study is being performed to compare the types of menstrual periods people with TS have when taking a type of progesterone called "Prometrium." In some teens and young adults with TS, their ovaries do not produce enough hormones. What researchers learn from this study could be used to help the care team find better treatments for teens and young adults whose ovaries do not make enough hormones.
Turner Syndrome Biorepository: A collection of clinical data and biological specimens to facilitate future research.
This study is being done for: • Children diagnosed with Turner Syndrome. • Parents and children who agree to participate in the collection of medical data and biological samples (e.g., blood collection, buccal swab)...
This study is being done for: • Children diagnosed with Turner Syndrome. • Parents and children who agree to participate in the collection of medical data and biological samples (e.g., blood collection, buccal swab). The TS biorepository study will facilitate and promote continuing research to improve health outcomes and lives of individuals with Turner syndrome and/or other differences in sex chromosomes.