NEBIDO in Symptomatic Late Onset Hypogonadism (SLOH)

Status Terminated

Clinical Trial Summary

The design of the study is a standard double-blind design, which is needed in this study to allow for unbiased evaluation of efficacy and safety. The effect of the additional impact of testosterone replacement therapy in hypogonadal men on muscle strength and quality of life in comparison to physical exercise alone will be assessed. Treatment duration will be 54 weeks, to monitor the increase as well as the "steady state" of the parameters assessed.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Hypogonadism

Clinical Trial Details

NCT number	NCT01092858
Study type	Interventional
Source	Bayer
Contact
Status	Terminated
Phase	Phase 4
Start date	September 2010
Completion date	July 2011

View Details

See also
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