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Primary Ovarian Insufficiency clinical trials

View clinical trials related to Primary Ovarian Insufficiency.

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NCT ID: NCT00471731 Completed - Menopause Clinical Trials

Dry Eye in Women With Turner Syndrome and Women With Premature Ovarian Failure

Start date: May 7, 2007
Phase: N/A
Study type: Observational

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.

NCT ID: NCT00443144 Completed - Turner Syndrome Clinical Trials

D3-GHR Polymorphism and Turner Syndrome

Start date: May 2005
Phase: N/A
Study type: Observational

The protein polymorphism of the growth hormone receptor characterized by the genomic deletion of exon 3 has been linked to the magnitude of the first-year-growth response to growth hormone (GH) in girls with Turner syndrome. Objective: to study the long-term effect of GH therapy in Turner syndrome in correlation to this GHR polymorphism in a mainly retrospective design (chart-review).

NCT ID: NCT00429494 Completed - Clinical trials for Premature Ovarian Failure

GnRH Analogue for Ovarian Function Preservation in Hematopoietic Stem Cell Transplantation Patients

Start date: November 2002
Phase: Phase 2
Study type: Interventional

Primary Objectives: - To determine the effectiveness of the 3-month depot leuprolide in inducing and maintaining secondary amenorrhea in patients undergo hematopoietic stem cell transplantation. - To determine the incidence of regained ovarian function manifested as spontaneous restoration of menstruation and normalization of hormonal level in patients after transplantation and discontinuation of long-acting leuprolide.

NCT ID: NCT00420654 Completed - Turner Syndrome Clinical Trials

Growth Hormone Treatment of Women With Turner Syndrome

Start date: August 2007
Phase: N/A
Study type: Interventional

Growth hormone treatment is used in girls with Turner syndrome to increase final height. The aim of this study is to evaluate the effect of growth hormone treatment on body composition and heart function in adult women with Turner syndrome. The hypothesis is that the fat mass will decrease and lean body mass will increase. There is only very limited documentation of the effect on the heart in this study population.

NCT ID: NCT00417157 Completed - Infertility Clinical Trials

Modified Natural Cycle Offers a Chance of Pregnancy in Patients With Poor Response and High Basal FSH

Start date: January 2007
Phase: Phase 4
Study type: Observational

The purpose of this study is to evaluate the effectiveness of a modified natural cycle in patients with previous poor response to infertility drugs and high basal FSH, prior to proceeding to oocyte donation or abandoning fertility treatment.

NCT ID: NCT00417066 Completed - Infertility Clinical Trials

Flexible GnRH Antagonist vs Flare up GnRH Agonist Protocol in Poor Responders

Start date: September 2003
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare ovulation induction using a flexible GnRH antagonist protocol and flare up GnRH agonist protocol in IVF patients with poor response to ovarian stimulation. Our hypothesis is that the antagonist protocol provides better IVF outcomes compared to the flare up protocol in this group of patients.

NCT ID: NCT00406926 Completed - Turner Syndrome Clinical Trials

The Effect of Growth Hormone in Very Young Girls With Turner Syndrome

Start date: August 1999
Phase: Phase 3
Study type: Interventional

This study investigated the effect of growth hormone on the growth of infants and toddlers with Turner syndrome during 2 years of treatment with growth hormone. This was compared with the growth of infants and toddlers with Turner syndrome who did not receive any growth hormone treatment. The overall aim was to prevent the growth failure usually seen during this period. The study also looked at middle ear disease, hearing problems, and cognitive and behavioral development.

NCT ID: NCT00295087 Completed - Clinical trials for Premature Ovarian Failure

X-Chromosome Inactivation Status and Premature Ovarian Failure

Start date: November 2005
Phase: N/A
Study type: Observational

Women who are affected with premature ovarian failure will exhibit skewed X-chromosome inactivation patterns compared to women with normal menstrual function (as defined by being pregnant), indicating a possible X-chromosome defect.

NCT ID: NCT00266656 Completed - Turner Syndrome Clinical Trials

Long-Term Growth and Skeletal Effects of Early Growth Hormone Treatment in Turner Syndrome

Start date: December 2005
Phase: Phase 4
Study type: Interventional

This is an extension study that will gather long-term data on the effect of early growth hormone (GH) treatment on adult height and other aspects of health and development in girls with Turner syndrome. The main purpose is to determine whether girls who received 2 years of GH treatment before 6 years of age achieve taller adult height than girls who were untreated during this time. The study will also look at middle ear and hearing function, and cognitive and behavioral development. Protocol completion is defined as attainment of height velocity less than or equal to 1.0 cm/year, or bone age greater than or equal to 15 years.

NCT ID: NCT00256126 Completed - Clinical trials for Growth Hormone Deficiency

Predictive Markers in Growth Hormone Deficiency (GHD) and Turner Syndrome (TS) Children Treated With SAIZEN®

Start date: May 31, 2005
Phase: Phase 4
Study type: Interventional

The study aims at identifying the predictive markers after one month of Saizen therapy in Growth Hormone Deficiency (GHD) and Turner Syndrome children.