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Testosterone Deficiency clinical trials

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NCT ID: NCT02082197 Withdrawn - Hypogonadism Clinical Trials

An Efficacy and Safety Study of ABT-SLV176 for the Treatment of Hypogonadal Men

Start date: March 2014
Phase: Phase 3
Study type: Interventional

This is an open-study with a 26 week open label treatment period followed by an optional 26 week open label extension. The total treatment period will be 52 weeks.

NCT ID: NCT01963390 Completed - Clinical trials for Testosterone Deficiency

Metabolomics During Testosterone Therapy

Start date: July 2012
Phase:
Study type: Observational

One promising but understudied area in the field of testosterone (T) therapy is its effect on metabolism and the development of type II diabetes. Metabolomics is a powerful research tool that can detect very early signs of metabolic derangement that may lead to metabolic disease. In this observational study, investigators aim to apply metabolomics in order to better understand how T therapy influences metabolism. In a clinical population of outpatient men with T deficiency investigators will perform comprehensive clinical evaluations and also obtain blood for metabolomics. This will be done once prior to T therapy and again after 4-6 months of T therapy. Investigators hypothesize that they can detect metabolic derangements in men with T deficiency and that these derangements will improve with T therapy.

NCT ID: NCT00858650 Completed - Clinical trials for Testosterone Deficiency

Registry of Hypogonadism in Men

RHyMe
Start date: March 2009
Phase: N/A
Study type: Observational

The primary objective of the Registry of HYpogonadism in MEn (RHYME) is to establish and maintain a large, multi-national prospective registry of male patients who have been diagnosed with male hypogonadism (HG), also known as androgen deficiency or testosterone deficiency.

NCT ID: NCT00512707 Completed - Diabetes Clinical Trials

Effect of Testosterone in Men With Erectile Dysfunction

TED
Start date: November 2006
Phase: Phase 4
Study type: Interventional

The purpose of this placebo-controlled study is to determine if testosterone replacement therapy, administered by transdermal gel, can improve the response to sildenafil (Viagra R) treatment in men who have erectile dysfunction (ED) and low testosterone levels.

NCT ID: NCT00494208 Completed - Menopause Clinical Trials

TDSM- Testosterone Dose Response in Surgically Menopausal Women

Start date: January 2009
Phase: N/A
Study type: Interventional

TDSM will study the physiology of testosterone in women ages 21-60 who have had surgical menopause (uterus and both ovaries removed). Testosterone is commonly thought of as a "male hormone" thus being that it is the male's primary hormone. Women produce testosterone in much smaller amounts and despite this, testosterone still plays a significant role. Fifty percent of a women's testosterone is made in her adrenal glands (glands that sit on top of the kidneys) and fifty percent is made in her ovaries. When a woman has her ovaries removed it is thought that her testosterone levels decrease rapidly and significantly. This study will be examining testosterone's role in sexual function, general well being, muscle performance, cognitive function, carbohydrate metabolism and muscle and fat distribution. The study is 14 months long with weekly to monthly visits. The subjects will be placed on the estrogen patch for the duration of the study. They will also be given weekly injections of testosterone or placebo for 6 months. During the testosterone treatment phase the women will be separated into 5 groups. The groups include a dose of testosterone that is very low, low, medium, high and placebo. A placebo looks and feels similar to testosterone; however it does not have testosterone in it. We use this to test if the subject is having a response to the testosterone itself or the thought of receiving testosterone. Neither the subject nor the investigators will know the dose until the end of the study.

NCT ID: NCT00280267 Completed - Muscle Weakness Clinical Trials

Testosterone Therapy After Hip Fracture in Elderly Women

Start date: August 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the feasibility of testosterone replacement therapy in frail elderly female hip fracture patients who have testosterone deficiency, and to obtain preliminary information about the effects of testosterone therapy on muscle strength and size, bone density, mobility, daily functioning, and quality of life.