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Adrenal Insufficiency clinical trials

View clinical trials related to Adrenal Insufficiency.

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NCT ID: NCT00552487 Completed - Clinical trials for Adrenal Insufficiency

Isolated ACTH Deficiency in Patients With Hashimoto Thyroiditis

Start date: October 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether patients with Hashimoto thyroiditis and impaired well-being may have a partial secondary adrenocortical insufficiency.

NCT ID: NCT00485186 Withdrawn - Clinical trials for Adrenal Insufficiency

Gene Polymorphisms Influencing Steroid Synthesis and Action

Start date: June 2007
Phase: N/A
Study type: Observational

The extend of steroid biosynthesis and action is mainly dependent on underlying genetic polymorphisms and gene mutations. These sequence variations in multiple genes involved in steroid biosynthesis and action cause different diseases (for example congenital adrenal hyperplasia or disorders of sex development). In addition, sequence variations in several other genes may influence the severity of a genetically caused disease of steroid biosynthesis or action. By this, the differences in an observed phenotype may be explained. Within the study all genes necessary for adrenal and gonadal steroid biosynthesis and several genes which are known to influence the action of steroid hormones will be analysed in patients with congenital disorders of adrenal and gonadal steroid biosynthesis, disorders of steroid action and disorders of sex development. The primary aim is to set up a correlation of the disease phenotype with the different genotypes detected.

NCT ID: NCT00471900 Completed - Clinical trials for Adrenal Insufficiency

Six Months DHEA Treatment in Female Adrenal Failure

Start date: October 2001
Phase: N/A
Study type: Interventional

DHEA is an adrenal deriven androgen precourser. The impact of DHEA substitution therapy in adrenal failure is unknown as well as the physiologically effects of DHEA is unknown. Effects of physiologically DHEA substitution is investigated in the model of female adrenal failure.

NCT ID: NCT00462644 Completed - Clinical trials for Adrenal Insufficiency

Evaluation of Etomidate on Adrenal Function in Trauma Patients

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

Trauma patients are at increased risk for adrenal function insufficiency. A commonly used agent for rapid sequence intubation (RSI) is known to decrease adrenal function. We want to determine the incidence of adrenocortical insufficiency and its significance during the first 24 hours of resuscitation following RSI in trauma patients.

NCT ID: NCT00444119 Completed - Clinical trials for Adrenal Insufficiency

Survey in Patients With Chronic Adrenal Insufficiency in Germany

Start date: May 2004
Phase: N/A
Study type: Observational

The purpose of this survey is to assess patients with chronic primary or secondary adrenal failure regarding subjective health status, incidence and causes of adrenal crisis, hormone replacement regimens and concomitant endocrine or non endocrine disease.

NCT ID: NCT00368381 Withdrawn - Sepsis Clinical Trials

Hydrocortisone Versus Hydrocortisone Plus Fludrocortisone for the Treatment of Adrenal Insufficiency in Severe Sepsis

Start date: September 2006
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if the combination of hydrocortisone plus fludrocortisone is more efficacious than hydrocortisone alone in treating adrenal insufficiency in severe sepsis.

NCT ID: NCT00364624 Completed - Lung Cancer Clinical Trials

Adrenal Function in Patients With Newly Diagnosed Lung Cancer

Start date: August 2006
Phase: N/A
Study type: Observational

Patients with newly diagnosed lung cancer may have hypofunction of the adrenal cortex either from tumour metastasis or other mechanisms. Since lung cancer patient may have to undergo stressful investigation and treatments, undetected hypofunction of the adrenal cortex may be hazardous. Knowledge of the size of the problem may help determine whether routine check is warranted.

NCT ID: NCT00185783 Completed - Sepsis Clinical Trials

Impact of Hydrocortisone Administration on White Blood Cell Gene Expression in Patients With Severe Sepsis

Start date: March 2005
Phase: Phase 1
Study type: Observational

The purpose of this pilot study is to (1) examine the changes in gene expression in patients who suffer from severe sepsis and whose shock (inadequate oxygen delivery to vital organs) state does not respond to fluid and vasopressor administration, (2) to show that our sampling method of isolating RNA provides reliable and consistent data, (3) provide a basis for future gene expression studies in critically ill patients

NCT ID: NCT00156767 Completed - Clinical trials for Adrenal Insufficiency

Adrenal Function in Critical Illness

Start date: November 12, 2004
Phase:
Study type: Observational

An appropriate hypothalamic-pituitary-adrenal (HPA) axis response is required to survive critical illness. Primary adrenal insufficiency, relative adrenal insufficiency, tissue resistance to glucocorticoids, ACTH deficiency and immune-mediated inhibition of the HPA axis may impair the secretion or action of glucocorticoids in critically ill patients. Adrenal insufficiency is estimated to occur in up to 77% of critically ill patients, but currently, there is no consensus on the diagnostic criteria for adrenal insufficiency in this setting, and standard testing does not discriminate among the aforementioned factors. We will study the incidence and natural history of adrenal insufficiency in critically ill patients to further define adrenal insufficiency and provide data to develop diagnostic tests. Clinical features and outcomes will be correlated with laboratory measurements of hormones, cytokines and glucocorticoid action. Healthy volunteers will undergo cortrosyn tests with measurement of free cortisol levels to develop a normative range for this endpoint. <TAB> Previous glucocorticoid use, if prolonged and supraphysiologic, also inhibits the HPA and can result in adrenal insufficiency. Patients with short intermittent courses of glucocorticoid administration have not been studied well, and may also be at risk. To gain further information about this group, patients receiving pulse glucocorticoid doses as part of bone marrow transplant regimens at the Clinical Center will also be studied. ...

NCT ID: NCT00005664 Terminated - Obesity Clinical Trials

Evaluation of Patients With Endocrine-Related Conditions

Start date: May 22, 2000
Phase:
Study type: Observational

This study will evaluate patients with a variety of endocrine disorders in order to 1) learn more about conditions that affect the endocrine glands (glands that secrete hormones) and 2) to train physicians in endocrinology. Patients of all ages with endocrine-related conditions may be eligible for evaluation under this protocol. Those enrolled may be required to provide blood, saliva, urine or stool samples, and to undergo ultrasound examination of the thyroid gland, ovaries or testes, adrenal glands or other parts of the body. Laboratory or X-ray studies may be done for diagnostic or treatment purposes. In some cases, patients will receive medical or surgical treatment for their disorder. Patients and family members of patients with a hereditary disorder may be asked to provide a blood sample for genetic analysis.