Clinical trial

Estrogen Dosing in Turner Syndrome:Pharmacology & Metabolism

Name
908-M01
Description
Estrogen is necessary for feminization during puberty and to decrease bone resorption, the latter critical for the achievement of peak bone mass and normal bone health in the female. The practicing pediatric endocrinologist often faces the dilemma of how to best feminize girls with hypogonadism (lack of estrogen), manifested as delayed or arrested puberty, due to disorders of the brain or the ovaries. We propose a series of studies to address which type, dose, and route of delivery of estrogen are suitable choices in feminizing and sustaining estrogen concentrations in adolescent girls with Turner syndrome. To accomplish this we will study girls/young woman between the ages of 13 to 20 with Turner Syndrome in 2 protocols. In Protocol # 1 we will study 24 girls with TS, they will receive 3 different estrogen preparations, either by mouth or via a patch for a total of 6 weeks. They will come to the clinical research center for blood draws after 2 wks of taking the estrogen. With this study, we hope to learn how the body responds to estrogen differently, depending on the form estrogen is given and how high, estrogen levels gets in the blood in these girls with Turner Syndrome. We will be comparing these patients estrogen levels to girls that menstruate normally and do not have Turner Syndrome. In Protocol #2, 40 patients with TS will be recruited; these patients will take estrogen for 1 year, either by mouth or via a patch. Patients will come to the lab for blood drawn in 7 occasions and we will measure estrogen levels as well as other hormones and lipid levels. We will also perform a Dual-energy X-ray absorptiometry (DXA) study (like an X ray) to assess body composition and bone mineralization. We will adjust doses based on the estrogen levels we find. With this study we hope to learn how estrogen affects body composition, i.e., the amount of fat vs. muscle, and how different forms of estrogen affect blood cholesterol and other hormones. This study will allow us to understand better how to best replace young woman with Turner Syndrome with estrogen.
Trial arms
Trial start
2009-01-01
Estimated PCD
2012-06-01
Trial end
2012-12-01
Status
Completed
Phase
Early phase I
Treatment
17 B estradiol orally
Group A will be given estrogen by mouth daily(0.5 mg or 1mg or 2 mg of 17B Estradiol. Doses will vary depending on the blood levels of estrogen starting with the lower doses and adjusting these doses up as needed to keep the levels in the normal range. The estrogen will be taken for 21 days. In order to have a menstrual cycle progesterone will be given for 7 days, starting from day 14 through day 21 of each cycle. Then both medications are stopped on day 21 for a total of 7 days. Labs will be obtained at baseline, 1,2,3,6,9 and 12 months. Dual-energy X-ray absorptiometry (DXA) scan and calorimetry will be done at baseline and at 6 and 12 month.
Arms:
Group A
Other names:
Estrace
17 B estradiol
Group B will be given estrogen via a patch applied to the skin twice a week (0.375mg or 0.05mg or 0.075mg) Doses will vary depending on the blood levels of estrogen starting with the lower doses and adjusting these doses up as needed to keep the levels in the normal range. The estrogen will be taken for 21 days. In order to have a menstrual cycle progesterone will be given for 7 days, starting from day 14 through day 21 of each cycle. Then both medications are stopped on day 21 for a total of 7 days. Labs will be obtained at baseline, 1,2,3,6,9 and 12 months. Dual-energy X-ray absorptiometry (DXA) scan and calorimetry will be done at baseline and at 6 and 12 month.
Arms:
Group B
Other names:
Vivelle
Size
41
Primary endpoint
Change in Weight From Baseline at 12 Months
12 months
Change in Body Mass Index From Baseline at 12 Months
12 months
Change in Percent Fat Mass From Baseline in 12 Months
12 months
Change in Fat Free Mass From Baseline at 12 Months
12 months
Eligibility criteria
Inclusion Criteria: * Girls with Turner Syndrome (45X, or related karyotypes) diagnosed clinically and cytogenetically * Female subjects with Y material will be allowed providing gonadectomies have been performed previously * Age: 13-20 years * Subjects have completed or nearly completed their linear growth * Previous growth hormone (GH) therapy discontinued at least 6 months prior to study participation * Stable thyroid replacement therapy will be allowed * Celiac disease on stable diets will be allowed * Any previous hormone replacement therapy (HRT) will be allowed Exclusion Criteria: * Diabetes Mellitus on insulin therapy, insulin sensitizers or oral hypoglycemics * Inflammatory Bowel Disease (ulcerative colitis or Crohn's disease), celiac disease * Cigarette smoking * Any other chronic conditions, that, in the opinion of investigators could impair the metabolism of nutrients * Severe obesity, i.e., Body Mass Index (BMI) \>95th centile
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE4'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 41, 'type': 'ACTUAL'}}
Updated at
2023-05-16

1 organization

1 product

3 indications

Indication
Turner syndrome
Indication
Hypogonadism