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Hypogonadism clinical trials

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NCT ID: NCT01560546 Completed - Clinical trials for Type 2 Diabetes Mellitus

Testosterone Therapy of Men With Type 2 Diabetes Mellitus (T2DM)

Start date: March 2012
Phase: Phase 4
Study type: Interventional

A randomized, placebo-controlled, double-blinded study on 40 men with type 2 DM. Type 2 diabetes mellitus (T2DM) is a common endocrine disorder characterized by hyperinsulinaemia and insulin resistance. Hypothesis Testosterone therapy increases lean body mass and insulin sensitivity in men with low normal levels of bioavailable testosterone and type 2 DM.

NCT ID: NCT01534208 Completed - Clinical trials for Secondary Hypogonadism

Safety Study of Enclomiphene Citrate in the Treatment of Men With Secondary Hypogonadism

Start date: May 2012
Phase: Phase 3
Study type: Interventional

ZA-300 is meant to determine the safety profile of Androxal (enclomiphene citrate) in men with secondary hypogonadism.

NCT ID: NCT01533129 Completed - Clinical trials for Hypogonadotrophic Hypogonadism

The Effect of Testosterone Replacement on Endothelial Dysfunction, Inflammation and Insulin Resistance in Male Hypogonadotrophic Hypogonadism

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

The study searched for answers to two questions 1. What is the effect of testosterone replacement therapy on endothelial dysfunction, inflammation and insulin resistance? 2. Regarding the above parameters, is there any difference between daily transdermal testosterone implementation and intramuscular injection performed in three weeks.

NCT ID: NCT01532414 Completed - Clinical trials for Secondary Hypogonadism

Phase III Study to Evaluated Morning Testosterone Normalization in Men With Secondary Hypogonadism

Start date: August 2012
Phase: Phase 3
Study type: Interventional

The purpose of ZA-301 is to determine the effects of Androxal on morning testosterone and reproductive status in younger overweight men with acquired hypogonadotropic hypogonadism (confirmed morning T<300 ng/dL) and normal sperm concentration, compared to changes with placebo. Subjects must not have previously been treated with testosterone products within the last 6 months.

NCT ID: NCT01454011 Completed - Clinical trials for Secondary Hypogonadism

The Effect of Testosterone Replacement on the High Density Lipoprotein Cholesterol Subgroups

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

The study is designed to answer the following questions: 1. Is there any difference between the compositions of the HDL cholesterol subpopulations of patients with hypogonadism and the healthy controls. 2. What is the effect of testosterone replacement therapy on the distributions of HDL subgroups. 3. Is there any difference between the effects of the two different testosteron replacement regiments

NCT ID: NCT01446042 Completed - Male Hypogonadism Clinical Trials

Safety and Efficacy of Intranasal TBS-1 Treatment of Male Hypogonadism

Start date: September 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the efficacy (based on the pharmacokinetic profile of testosterone) and safety of TBS-1 in the treatment of hypogonadal men

NCT ID: NCT01438073 Completed - Clinical trials for Hypogonadotropic Hypogonadism

Elucidating Kisspeptin Physiology by Blocking Kisspeptin Signaling

Start date: September 2011
Phase: Phase 1
Study type: Interventional

The investigators are looking for subjects to complete a study on the role of kisspeptin in the reproductive system. Kisspeptin is a naturally occurring hormone in humans that tells the body to produce other reproductive hormones. However, giving someone a continued amount of kisspeptin over a period of time can have the opposite effect and tell the body to, for a short time, stop making hormones needed for reproduction. By giving 24-hour infusions of kisspeptin, the investigators hope to learn more about the role kisspeptin has in the way bodies function normally and the role it has in conditions that affect the reproductive system.

NCT ID: NCT01438034 Completed - Clinical trials for Hypogonadotropic Hypogonadism

Kisspeptin in the Evaluation of Delayed Puberty

Start date: June 8, 2013
Phase: Phase 1
Study type: Interventional

The goal of this study is to test whether the hormone kisspeptin has the potential to prospectively diagnose adolescents with self-resolving or permanent delayed puberty. Some children with delayed puberty will eventually enter puberty on their own. However, some children with delayed puberty have a permanent condition and require medical treatment to undergo puberty. Right now, there is no reliable diagnostic tool to tell whether a child's delayed puberty will be self-resolving or permanent. The hormone kisspeptin has the potential to prospectively diagnose adolescents with self-resolving or permanent delayed puberty.

NCT ID: NCT01419236 Completed - Hypogonadism Clinical Trials

A Study of Ejaculatory Dysfunction in Men With Low Testosterone Levels

Start date: August 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to see if testosterone solution 2% can impact symptoms of ejaculatory dysfunction in men with low testosterone.

NCT ID: NCT01403532 Completed - Clinical trials for Hypogonadotropic Hypogonadism

Sequential Therapy for Hypogonadotropic Hypogonadism

Start date: September 2009
Phase: Phase 4
Study type: Interventional

The traditional therapy for induction of spermatogenesis in male hypogonadotropic hypogonadism requires both HCG and human menopausal gonadotropin (HMG) or FSH until pregnancy occurs. Because of the high cost of hMG or FSH preparations and poor compliance, the investigators raise a new sequential therapeutic approach which can make the treatment more economic and tolerable. The zinc supplement will be also evaluated in patients in this study. This randomized, parallel, open, and multi-center study will compare the efficacy of traditional therapy with new therapy and evaluate the safety of the new protocol.