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Hypogonadism clinical trials

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NCT ID: NCT01323140 Completed - Hypogonadism Clinical Trials

Pharmacokinetics, Metabolism, Efficacy, and Safety Study of Two Testosterone Matrix Transdermal Systems

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

Watson's testosterone transdermal system delivers male sex hormone through skin for the treatment of men with sex hormone insufficiency.

NCT ID: NCT01270841 Completed - Clinical trials for Secondary Hypogonadism

Normalization of Morning Testosterone Levels in Men With Secondary Hypogonadism

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

The Purpose of the study is to determine the effects of Androxal on morning testosterone and reproductive status in men with secondary hypogonadism(confirmed morning Testosterone less than 250 ng/dL), compared to changes with placebo, or Testim (topical testosterone). The effects of Testim versus placebo on reproductive status will also be examined. Study subjects must not be currently using a topical testosterone.

NCT ID: NCT01252745 Completed - Hypogonadism Clinical Trials

Efficacy of an Intranasal Testosterone Product

Start date: August 2010
Phase: Phase 2
Study type: Interventional

This clinical trial will compare the pharmacokinetic profile of testosterone after repeated intranasal administration of TBS-1 of different strengths in subjects with hypogonadism

NCT ID: NCT01228071 Completed - Male Hypogonadism Clinical Trials

Time to Eugonadal Range, Time to Steady State and Drying Time

Start date: November 2010
Phase: Phase 3
Study type: Interventional

This is a multicenter, open-label, single arm trial to evaluate the time to eugonadal testosterone range after initial testosterone gel 2% application, time to steady state after after initiation of testosterone gel 2%, and drying time after application of testosterone gel 2%.

NCT ID: NCT01206270 Completed - Clinical trials for Klinefelter Syndrome

Androgen for Leydig Cell Proliferation

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

Patients with infertility often presents alterations at ultrasonographic examination of the testis. These alterations include a much higher incidence of small, multiple, non-palpable hypoechoic micro-nodules that can show internal vascularization. This finding often create alarm and anxiety, because it has to be placed in a differential diagnosis versus low-stage malignant germ cell tumors. Nevertheless, explorative surgery reveal that a consistent number of these lesion are benign, due to Leydig cell hyperplasia or Leydig cell tumours. The purpose of this study is to evaluate the effects of androgen therapy on the size and number of non-palpable hypoechoic micro-nodules in patients with elevated gonadotropin levels.

NCT ID: NCT01200862 Terminated - Clinical trials for Obese Hypogonadotropic Hypogonadism

Safety and Efficacy of BGS649 in Obese, Hypogonadotropic Hypogonadal Men

OHH
Start date: August 2010
Phase: Phase 2
Study type: Interventional

This study is designed as a 2-part study, with Part 1 being open-label to best determine the appropriate dose levels to use in Part 2, which has a randomized, double-blind, placebo controlled design. The study aims to assess the safety and tolerability of BGS649, and determine whether or not BGS649 is able to normalize testosterone levels and improve insulin sensitivity in obese, hypogonadotropic hypogonadal (OHH) men

NCT ID: NCT01191320 Completed - Clinical trials for Type 2 Diabetes Mellitus

Study to Evaluate the Efficacy of Androxal in Controlling Blood Glucose in Men With Type-2 Diabetes Mellitus

Start date: October 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the effect the investigative drug has on glycemic control in men with type 2 diabetes mellitus (T2DM) and secondary hypogonadism

NCT ID: NCT01172366 Completed - Hypogonadism Clinical Trials

A Study to Evaluate the Potential for Interpersonal Transfer of Testosterone Following Single Dose Application

Start date: August 2010
Phase: N/A
Study type: Observational

The hypotheses for this study is that there is no transfer of testosterone from male (donor) subjects to female (recipient) subjects when contact is made 2 hours post application of 2% Testosterone MD-Lotion® if the donor has a covered application area with a T-shirt.

NCT ID: NCT01165619 Terminated - Clinical trials for Idiopathic Hypogonadotropic Hypogonadism

Detailed Clinical, Biochemical and Genetic Characterization in Gonadotropin-releasing Hormone (GnRH) Deficiency Disorders

Start date: June 2010
Phase: N/A
Study type: Observational

In this study, we will measure levels of reproductive hormones and metabolic markers in subjects with isolated GnRH deficiency disorders and compare them to healthy control populations. Our goals are (1) to chart the range of hormonal and metabolic biomarkers in healthy subjects and those with reproductive disorders and (2) to correlate reproductive and metabolic phenotypes with genetic changes within patients with reproductive disorders and healthy controls.

NCT ID: NCT01160341 Completed - Hypogonadism Clinical Trials

Metabolic Syndrome Criteria and the Effect of Testosterone Treatment in Young Men With Hypogonadism

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

The study is designed to answer the following questions: 1. Is hypogonadism a cause for the metabolic syndrome ? 2. What is the effect of testosterone replacement on the metabolic parameters ?