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| Sponsor: | National Eye Institute (NEI) |
|---|---|
| Information provided by: | National Institutes of Health Clinical Center (CC) |
| ClinicalTrials.gov Identifier: | NCT00471731 |
Purpose
Women with premature ovarian failure (POF) are at risk for dry eye. In addition, some women with Turner syndrome (TS) report dry eye symptoms. This study will determine how many women with TS have dry eye, compared to women with POF and women without these conditions.
Females 16 years of age and older with TS, POF, or neither of these conditions may be eligible for this study. Participants undergo the following tests and procedures:
| Condition |
|---|
|
Turner Syndrome Ovarian Failure, Premature Sex Chromosome Aberrations Menopause Perimenopause |
| Study Type: | Observational |
| Study Design: | Time Perspective: Prospective |
| Official Title: | Ocular Impact of X Chromosome Karyotype and Sex Hormones in Turner Syndrome and Premature Ovarian Failure |
| Estimated Enrollment: | 180 |
| Study Start Date: | May 2007 |
Premature ovarian failure (POF) is known to be associated with an increased risk of ocular surface disease (dry eye), likely due to the reduction of both estrogens and androgens seen in this condition. From preliminary data, we suspect that women with Turners syndrome (45, XO), a genetic abnormality that affects sex hormone levels, are also at increased risk of ocular surface disease. Comparing POF and TS women may allow us to distinguish different mechanisms for ocular surface disease, due to the different etiologies of hormonal (estrogen and androgen) alterations posed by POF and TS.
Eligibility| Ages Eligible for Study: | 16 Years and older |
| Genders Eligible for Study: | Female |
| Accepts Healthy Volunteers: | Yes |
INCLUSION CRITERIA:
EXCLUSION CRITERIA:
Contacts and Locations| Contact: Patient Recruitment and Public Liaison Office | (800) 411-1222 | prpl@mail.cc.nih.gov |
| Contact: TTY | 1-866-411-1010 |
| United States, Maryland | |
| National Institutes of Health Clinical Center, 9000 Rockville Pike | Recruiting |
| Bethesda, Maryland, United States, 20892 | |
| Sub-Investigator: Patient Recruitment and Public Liaison Office (PRPL) For more information at the NIH Clinical Center contact | |
More Information
| ClinicalTrials.gov Identifier: | NCT00471731 History of Changes |
| Other Study ID Numbers: | 070145, 07-EI-0145 |
| Study First Received: | May 9, 2007 |
| Last Updated: | December 21, 2011 |
| Health Authority: | United States: Federal Government |
|
Ocular Surface Disease Imprinting Eye Abnormalities Ovarian Insufficiency Women's Eye Health and Disease Turner Syndrome |
TS Premature Ovarian Failure POF Healthy Volunteer HV |
|
Chromosome Aberrations Chromosome Disorders Menopause, Premature Primary Ovarian Insufficiency Sex Chromosome Aberrations Turner Syndrome Gonadal Dysgenesis Pathologic Processes Congenital Abnormalities Genetic Diseases, Inborn Ovarian Diseases Adnexal Diseases |
Genital Diseases, Female Gonadal Disorders Endocrine System Diseases Disorders of Sex Development Urogenital Abnormalities Sex Chromosome Disorders of Sex Development Heart Defects, Congenital Cardiovascular Abnormalities Cardiovascular Diseases Heart Diseases Sex Chromosome Disorders |