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Hypothyroidism clinical trials

View clinical trials related to Hypothyroidism.

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NCT ID: NCT04878614 Terminated - Hypothyroidism Clinical Trials

Comparison of Levothyroxine Formulation in Hypothyroid Patients With Enteral Feeding

Start date: May 5, 2021
Phase: Phase 4
Study type: Interventional

The purpose of this study is to test a liquid levothyroxine formula and examine if it will lead to improvement in management of thyroid function and if it improves hypothyroid symptoms that patients experience.

NCT ID: NCT04747275 Terminated - Hypothyroidism Clinical Trials

Use of Liquid Stable Levothyroxine in Trisomy 21 Pediatric Patients

Start date: January 18, 2021
Phase: Phase 4
Study type: Interventional

Children with levothyroxine (T21) have developmental delay and other functional gastrointestinal (GI) issues that may negatively affect L-T4 tolerability and absorption. For an age group unable to swallow tablets whole by mouth, tablets must be crushed and suspended in water, breast milk or formula for administration in order to treat children with hypothyroidism. For this age group, ease of administration may have a significant impact on compliance and ability to remain euthyroid. We propose that Tirosint-SOL® will be more favorably received due to ease of administration, improved tolerability and palatability, therefore leading to improved adherence when compared to L-T4 tablets.

NCT ID: NCT02946918 Terminated - Thyroid Cancer Clinical Trials

Levothyroxine Replacement With Liquid Gel Capsules vs Tablets Post-thyroidectomy

Start date: February 1, 2017
Phase: Phase 4
Study type: Interventional

In some patients, levothyroxine liquid gel capsules may demonstrate superior absorption than the tablet option. Impaired absorption of thyroid hormone directly correlates to higher and more unpredictable TSH (thyroid stimulating hormone) levels. The investigators therefore hypothesize that following thyroidectomy for Stage I/II differentiated thyroid cancer the gel capsule levothyroxine formulation will provide more predictable TSH results and in turn require fewer dose adjustments to achieve optimal hormone levels in the postoperative period. The aim of this investigation is to compare the use of levothyroxine in liquid gel capsules to tablet form for TSH suppression following thyroidectomy for presumed stage I/II differentiated thyroid cancer.

NCT ID: NCT02567877 Terminated - Hypothyroidism Clinical Trials

Is Levothyroxine Alone Adequate Thyroid Hormone Replacement?

Start date: November 2016
Phase:
Study type: Observational

Patients taking thyroid hormone replacement after thyroid removal surgery often report feeling differently than they did prior to taking thyroid hormone. The symptoms can include fatigue, worsening mood or subjective "brain fog" where the patient feels like their thinking is just not as sharp as it was previously. Multiple studies have found that patients taking thyroid hormone replacement have a diminished quality of life compared to matched controls. Previous studies have suggested that the type of deiodinase (DIO) polymorphism a patient has, which is responsible for converting the thyroid hormone T4 into the more biologically active T3, may contribute to their overall cognition and sense of well-being. The Investigators aim to determine if the type of deiodinase polymorphism a patient has contributes to the patient's cognition and overall sense of well-being after surgery and thyroid hormone replacement. Objective: Determine if patients with the deiodinase type 2 CC polymorphism have objective differences in working memory (N-back test is primary endpoint), cognitive function and sense of well-being after thyroidectomy when placed on standard thyroid hormone replacement therapy. Hypotheses: (1) Patients with the deiodinase type 2 CC polymorphism will have worse working memory (N-back test is primary endpoint), cognitive function and sense of well-being on standard thyroid hormone replacement therapy after thyroidectomy compared with before thyroidectomy. (2) Patients with the deiodinase type 2 TT or TC polymorphism will have no differences in working memory, cognitive function or sense of well-being on standard thyroid hormone replacement before and after thyroidectomy.

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: 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: NCT00488644 Terminated - Brain Tumor Clinical Trials

Combined Levothyroxine/Liothyronine Supplementation in Hypothyroid Patients With Brain Tumors

Start date: February 2006
Phase: N/A
Study type: Interventional

Primary Objectives: 1. Assess whether combined treatment with Levothyroxine and Liothyronine improves learning and memory. 2. Explore the relationship between T3 treatment and other domains of cognitive function, quality of life, and mood.

NCT ID: NCT00206375 Terminated - Hypothyroidism Clinical Trials

Growth Hormone and GnRH Agonist in Adolescents With Acquired Hypothyroidism

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

The purpose of this study is to see if giving growth hormone and Lupron along with thyroid hormone will improve final height in patients with long term hypothyroidism. Lupron is a medicine which is used to delay puberty and to prevent early closure of growing bones which might increase growth potential. Growth hormone is used to restore growth rate. This study will include children with "short term" and "long term" hypothyroidism.