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Hypothyroidism clinical trials

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NCT ID: NCT00962221 Terminated - Clinical trials for Subclinical Hypothyroidism

Lipids Profile in Subclinical Hypothyroidism

LPSH
Start date: October 2009
Phase: N/A
Study type: Observational

Overt hypothyroidism is associated with increased risk for cardiovascular disease (CVD) as indicated by hypertension, hypercholesterolemia, and increased low-density lipoprotein cholesterol (LDL-C) levels. Mild hypothyroidism, also called subclinical hypothyroidism [SH] is highly prevalent in elderly subjects, especially in women older than 50 years of age. Whether SH is related as a risk for premature CVD is controversial. It was shown that SH is associated with elevated lipids levels, particularly LDL-cholesterol. However recent evidence suggests that the 'quality' rather than only the 'quantity' of LDL-cholesterol exerts a direct influence on the cardiovascular risk. LDL-cholesterol comprises multiple distinct subclasses that differ in their atherogenic potential. Thus, the proposed study protocol is intended to evaluate the different LDL lipoproteins subclasses in patients with subclinical hypothyroidism.

NCT ID: NCT00921050 Completed - Clinical trials for Subclinical Hypothyroidism

Subclinical Hypothyroidism and Mind in the Elderly

Start date: June 2009
Phase: Phase 2/Phase 3
Study type: Interventional

Some recommendations of expert consensus on subclinical hypothyroidism (SH) are controversial in those areas with not enough information to reach a conclusion, such as not recommending treatment with thyrotrophic hormone of 4-10 mUI/L and free thyroxin in normal range. The body changes or symptoms at this stage are often mistaken as aging. There are studies showing significant changes in heart (slow rate, lower ejection fraction, diastolic dysfunction); hypercholesterolemia, dysfunction cognitive abilities (memory attention…). The prevalence of SH increases with age, reaching 14% over 65 years old. This age group increase as the population ages highlights the need for evidence to improve recommendations for the elderly. NEUROPSI is a validated neuropsychological test sensible for mild cognitive alterations. It can be applied to individuals with little schooling. This study aims to determine positive change in cognitive abilities (NEUROPSI), ejection fraction, and body percent of lean and adipose tissue without adverse effects, placebo versus thyroxin supplement to keep thyroid-stimulating hormone (TSH) between 0.5-2.5 mUI/L in elderly with TSH 4-10 mIU/L.

NCT ID: NCT00818896 Completed - Hypothyroidism Clinical Trials

Maternal Hypothyroidism in Pregnancy

Start date: April 2008
Phase: N/A
Study type: Observational

There is general agreement that thyroid gland function should be assessed in pregnant women. When the gland produces too little thyroid hormone (hypothyroidism), all of the woman's bodily functions slow down, and there are problems with her baby's development. Until now, physicians have identified this problem on an individual basis (case-finding), but this approach misses many of the cases. Our trial aims to replace case-finding with a routine blood test that is highly effective at detecting hypothyroidism, thereby allowing treatment to correct the deficiency. This approach can eventually be implemented throughout the United States.

NCT ID: NCT00770016 Terminated - Hypothyroidism Clinical Trials

Insulin Sensitivity and Metabolism Before and After Treatment in Patients With Hypothyroidism

Start date: January 2010
Phase: N/A
Study type: Interventional

The aim of this study is to further characterize the treatment related changes in insulin sensitivity, substrate metabolism and intra hepatic- and intramyocellular lipid content in patients with hypothyroidism

NCT ID: NCT00747760 Completed - Hypothyroidism Clinical Trials

TSH Receptor Mutations Among a Consanguineous Community

TSHR
Start date: December 2005
Phase: N/A
Study type: Observational

Resistance to thyrotropin (RTSH) is a condition of impaired responsiveness of the thyroid gland to TSH, characterized by elevated TSH, low or normal thyroid hormone levels, and hypoplastic or normal-sized thyroid gland. The aim of the present study was to evaluate the clinical course over time,the genotype-phenotype association and the frequency of two different TSH-receptor (TSHR) mutations in a highly consanguineous population of the town of Um-El-Fahem.

NCT ID: NCT00715572 Completed - Hypothyroidism Clinical Trials

Combined Therapy With L-Thyroxine and L-Triiodothyronine Compared to L-Thyroxine Alone

Start date: March 2002
Phase: N/A
Study type: Interventional

The objective of this study was to analyze the features of monotherapy with L-T4 in comparison with combined therapy with L-T4 and L-T3 in patients with primary hypothyroidism.

NCT ID: NCT00565864 Completed - Hypothyroidism Clinical Trials

Neurocognitive and Metabolic Effects of Mild Hypothyroidism

Start date: August 2008
Phase: Phase 4
Study type: Interventional

Patients with hypothyroidism are routinely treated with thyroid hormone (l-thyroxine) for replacement therapy. Physicians monitor the thyroid hormone dose by measuring a thyroid stimulating hormone (TSH) level in the blood, with the goal of a normal level. However, recent data suggest that the "normal" TSH range is too broad, and that patients may still have symptoms if their TSH levels are at the top or bottom part of the normal range. To study this issue, it is useful to address issues such as general health status, psychological symptoms, mood, memory, and metabolic status, since thyroid hormone has major effects on the brain and metabolism, and since patients with treated hypothyroidism often have symptoms related to these areas. In the present study, otherwise healthy subjects with treated hypothyroidism, ages 20-75 years, will be enrolled in a 7-11month study. At baseline, they will have tests of health status, psychological symptoms, mood, memory, body composition, and energy expenditure performed. Following these baseline measurements, subjects will receive either their usual doses of l-thyroxine, or a slightly higher or lower dose. The doses will be chosen to try to achieve either a low-normal TSH level, a high-normal TSH level, or a mildly elevated TSH level. Which target TSH the patient is assigned will be determined randomly, and neither the subject nor the study contacts will know which dose the patient is receiving. Subjects will be seen every 6 weeks during the study for brief visits to make sure they are not having any side effects, and to adjust the l-thyroxine doses if the TSH has not yet reached the target range. At the 24-week visit (end of study), the subjects will undergo the same tests that they had on the baseline visit. Results from the study will be examined to see if minor changes in TSH or other thyroid hormone levels cause changes in any of the outcomes, and if the degree of TSH change correlates with the degree of outcome changes. These results may help physicians caring for patients with thyroid disease better determine the optimal dose of thyroid hormone for each patient.

NCT ID: NCT00535561 Completed - Clinical trials for Iron Deficiency Anemia

Iron Deficiency Anemia Can be an Indication for Treatment of Subclinical Hypothyroidism

Start date: June 2007
Phase: Phase 1
Study type: Interventional

To determine whether iron deficiency anemia can be an indication for the treatment of subclinical hypothyroidism.

NCT ID: NCT00531713 Completed - Depression Clinical Trials

Effect of T4-T3 Combination Therapy Versus T4 Monotherapy in Patients With Hypothyroidism

T4-T3
Start date: April 2003
Phase: Phase 4
Study type: Interventional

To compare the effect of T4-T3 combination therapy versus T4 monotherapy in patients with autoimmune hypothyroidism, on stable T4-substitution therapy

NCT ID: NCT00524238 Completed - Hypothyroidism Clinical Trials

Metabolic Changes in Hypothyroid Patients

Start date: March 2004
Phase: N/A
Study type: Interventional

Hypothyroidism is a frequent condition in danish women, but often overlooked. Along with fatigue one of the main symptoms is weight gain as a result to significantly decreased energy expenditure. This study was undertaken to elucidate changes in glucose, lipid and amino acid turnover in these patients.