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OpenTrials
Completed

NCT Number: NCT00304746

AndroGel in Men With Major Depression and Incomplete Response to Antidepressant Treatment

We hypothesize that AndroGel may offer some relief to subjects with low or borderline testosterone levels who suffer from depression and have failed to respond to a trial of a standard antidepressant.

During this nine week, outpatient, double-blind study, male subjects between the ages of 30 and 65 years with treatment-refractory depression and low or borderline low testosterone levels will be treated with either AndroGel or placebo. Following this nine week, double-blind phase, eligible subjects will have the option to continue into a six month, open-label phase during which time all subjects will receive the AndroGel patch.

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Key information

Age range

30 year–65 year

Sex eligibility

Male

Study type

Interventional

Phase

Phase 4

Primary location

The Chaim Sheba Medical Center, Tel Litwinsky, Israel

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About this study

We will recruit 100 men between the ages of 30 and 65 years who have treatment-refractory depression and low or borderline low testosterone levels for participation in this study. For a period of nine weeks subjects will receive double-blind treatment with either AndroGel (testosterone gel) or placebo. During this double-blind treatment phase subjects will come to McLean Hospital for a total of seven visits. Both clinical assessments (including ratings of your levels of depression and anxiety, quality of life, and visuospatial memory)and laboratory tests will be performed at these visits. Following the nine week, double-blind phase, eligible subjects may enter into a six month, open-label treatment phase in which all subject receive AndroGel. If you participate in the open-label phase, you will be asked to return to the site for 8 visits during the six month period.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male
  • 30-65 years old
  • Taking at least one serotonergic antidepressant at adequate dose for at least six weeks but still meeting DSM-IV criteria for major depressive disorder within the past year
  • HAM-D score >12

Exclusion criteria

  • Current suicidal ideation
  • Substance abuse or dependence within the past year
  • Current or past psychotic symptoms
  • A history of bipolar disorder
  • A prostate-specific antigen (PSA) level greater than 4.0 ng/ml
  • Other clinically significant medical condition
  • A history of failing to show any clinically significant response to two or more adequate trials of different antidepressants.

Treatment and study plan

Testosterone gel

Drug

AndroGel 2.5g and 5g sachets at doses ranging from 10g/day for duration of trial.

Other names: AndroGel

Placebo

Drug

Placebo

Primary outcomes

  1. 21-item Hamilton Depression Rating Scale Score (HAM-D)

    Time frame: 9 weeks (1-week placebo lead-in and 8 weeks of blinded medication treatment)

    The HAM-D generates a score ranging from 0 (no depressive symptoms) to 64 (most severe depression).

Secondary outcomes

  1. Montgomery Asberg Depression Rating Scale (MADRS)

    Time frame: 9 weeks (1 week of placebo lead-in and 8 weeks of blinded medication treatment)

    The Montgomery Asberg Depression Rating Scale (MADRS) is a clinician-assessed scale that rates depressive symptoms on a scale from 0 (no depressive symptoms) to 60 (maximal depressive symptoms).

Sponsors and collaborators

Lead sponsor

Mclean Hospital

Other

Collaborators

  • Solvay Pharmaceuticals

Registry information

Official study title

A Parallel-Group, Placebo-Controlled Trial of AndroGel in Men With Major Depressive Disorder Who Display an Incomplete Response to Standard Antidepressant Treatment

Important dates

Study start
2006
Primary completion
2008
Study completion
2009
First posted
Mar 20, 2006
Registry last updated
Nov 24, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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