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Turner Syndrome clinical trials

View clinical trials related to Turner Syndrome.

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NCT ID: NCT00250250 Completed - Turner's Syndrome Clinical Trials

An Open-Label, Multi-centre, Phase III Study of Local Tolerability of ZOMACTON 10MG

Start date: October 2005
Phase: Phase 3
Study type: Interventional

Children with growth failure due to inadequate secretion of growth hormone or growth retardation due to Turner's syndrome are individually dosed and treated for 12 weeks

NCT ID: NCT00234533 Completed - Clinical trials for Renal Insufficiency, Chronic

Study to Define Optimal IGF-1 Monitoring in Children Treated With NutropinAq

OPTIMA
Start date: June 2004
Phase: Phase 3
Study type: Interventional

The main purpose of this study is to establish an optimal monitoring regimen in NutropinAq treated children, using newly developed capillary blood spot IGF-1 measurement technology.

NCT ID: NCT00191113 Completed - Turner Syndrome Clinical Trials

Somatropin Treatment to Final Height in Turner Syndrome

GDCT
Start date: February 1989
Phase: Phase 3
Study type: Interventional

A randomized, controlled trial in girls with Turner syndrome at least 7 years old and younger than 13 at study entry, to determine the efficacy and safety of Humatrope (somatropin) treatment in promoting linear growth to final height.

NCT ID: NCT00140998 Completed - Hypogonadism Clinical Trials

Estrogen Treatment (Oral vs. Patches) in Turner Syndrome

Start date: January 2001
Phase: Phase 3
Study type: Interventional

The study attempts to evaluate if the way of administering estrogen, the principal female hormone, via patches or orally, affects the way estrogen works in girls with Turner Syndrome. These are girls who are very short and whose ovaries do not work. We will examine changes bone, protein and fat metabolism under the influence of estrogen delivered by a patch trough the skin vs estrogen taken orally. These studies are conducted while the girls are taking GH therapy.

NCT ID: NCT00134745 Completed - Turner Syndrome Clinical Trials

Defining the Optimal Hormonal Replacement Therapy in Turner Syndrome

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

The purpose of this study is to examine whether a larger dosage of estrogen than the one used today will secure the development of a normal sized uterus and increase the strength of the bones in girls and young women with Turner syndrome. The purpose is also to evaluate whether aortic dilatation is present in this group of patients, and if the estrogen dosage will influence the emotional well-being and self-esteem of the patients.

NCT ID: NCT00121875 Terminated - Turner Syndrome Clinical Trials

Study to Identify Markers of Insulin Resistance During Growth Hormone Treatment for Short Stature

Start date: June 2005
Phase: Phase 4
Study type: Observational

Growth hormone treatment improves body fat distribution but also causes insulin resistance. Scientists have recently linked insulin resistance with special stores of fat in the muscles, which can be measured by magnetic resonance imaging (MRI). The researchers hypothesize that growth hormone will paradoxically reverse the linkage between muscle fat stores and insulin resistance. To assess this association and to investigate the cause(s), the researchers will measure muscle fat stores during growth hormone treatment. Other parameters linked to insulin resistance (glucose tolerance, blood markers, and body composition) will also be assessed. This study may lead to improved strategies for monitoring growth hormone therapy.

NCT ID: NCT00097552 Completed - Turner Syndrome Clinical Trials

A Study to Evaluate Subjects With Turner Syndrome Treated With Growth Hormone

Start date: May 1997
Phase: Phase 4
Study type: Observational

This study is a multicenter, open-label, observational, postmarketing surveillance study of Genentech growth hormone (GH) products in the treatment of girls with Turner syndrome in the United States and Canada.

NCT ID: NCT00097526 Completed - Turner Syndrome Clinical Trials

Bone Mineral Density (BMD) in Adolescents With Growth Hormone Deficiency (GHD)

Start date: April 2000
Phase: Phase 4
Study type: Observational

This study is a multicenter, open-label, postmarketing surveillance study. The substudy will collect information on BMD in adolescents and young adults with GHD or Turner syndrome who are completing GH treatment for statural indications.

NCT ID: NCT00029159 Completed - Turner Syndrome Clinical Trials

The Effect of Androgen and Growth Hormone on Height and Learning in Girls With Turner Syndrome

Start date: November 1992
Phase: Phase 3
Study type: Interventional

The purposes of this study are to learn whether treatment with an androgen type hormone will improve the visual-spatial problems associated with Turner syndrome, and to evaluate the effect growth hormone, with and without androgen, has on growth.

NCT ID: NCT00013546 Completed - Osteoporosis Clinical Trials

Hormone Replacement Therapy to Treat Turner Syndrome

Start date: March 2001
Phase: Phase 2
Study type: Interventional

This study will evaluate the effects of hormone replacement therapy on patients with Turner syndrome (TS)-a genetic disorder in females in which part or all of one X chromosome is missing. Most girls and women with TS have underdeveloped ovaries-the female reproductive organs that produce the female sex hormones estrogen and progesterone, and smaller amounts of the male sex hormone, testosterone. These hormones affect muscle and bone strength, sex drive, energy, and an overall sense of well being. Estrogen may also play a role in memory and mood and have a protective effect against heart disease. Women with TS have a much higher risk of developing osteoporosis (loss of bone density), high blood pressure, high cholesterol and diabetes than women without this disorder. Girls and women with Turner syndrome between the ages of 14 and 50 years may be eligible for this 2-year study. Three months before beginning treatment, all patients will wear an estrogen patch and take a progesterone tablet daily for 10 days each month. They will then be randomly assigned to one of two treatment groups to compare the effects of estrogen alone with estrogen plus testosterone on bone strength, muscle and fat mass and psychosocial well being. Both groups will wear an estrogen patch and take oral progesterone. One group will also wear a testosterone patch while the other group will wear a placebo patch (a patch that does not contain any testosterone). Neither study participants nor the doctors will know who is getting the testosterone until the study is complete. Patients will undergo the following procedures before beginning treatment and at 6, 12 and 24 months after starting treatment: - Physical examination. - DEXA scans (dual energy X-ray absorptiometry) to measure body composition and bone thickness. Low radiation X-rays scan the whole body to measure fat, muscle and bone mineral content.. - Magnetic resonance imaging (MRI) scan of the abdomen to measure the amount of fat around the internal organs. The patient lies on a stretcher in a large tube surrounded by a magnetic field during the scanning. The procedure uses a strong magnet and radio waves to produce the images. - Heel ultrasound to measure bone thickness. The heel is placed in a chamber and sound waves pass through it to produce images. - Oral glucose tolerance test (OGTT) for diabetes and problems with carbohydrate metabolism. The patient drinks a sugary substance. A small amount of blood is drawn before taking the drink and four times afterwards. - Blood and urine tests to measure blood counts, liver and kidney function, ovarian hormones, growth factors, thyroid function, blood lipids, bone strength markers, and to test for pregnancy. - Blood pressure measurements. - Psychological testing for the effect of treatment on mood, self-esteem, quality of life, social shyness, anxiety and sexual function. - Neurocognitive tests (at first inpatient visit and 1 and 2 years after starting treatment) to measure nonverbal memory and visual-perceptual abilities. During the hospital admissions, patients will be given a "metabolic diet" that contains specific amounts of salt and carbohydrates to ensure accurate blood pressure and sugar metabolism measurements. Patients will keep a record of their menstrual periods and physical activity throughout the treatment period.