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

Primary Purpose

Depressive Disorder, Major

Status
Completed
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Testosterone gel
Placebo
Sponsored by
Mclean Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Depressive Disorder, Major

Eligibility Criteria

30 Years - 65 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

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.

Sites / Locations

  • McLean Hospital
  • The Chaim Sheba Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

testosterone gel

placebo gel

Arm Description

AndroGel (1% testosterone transdermal gel), 2.5 g to 10 g daily

Placebo gel

Outcomes

Primary Outcome Measures

21-item Hamilton Depression Rating Scale Score (HAM-D)
The HAM-D generates a score ranging from 0 (no depressive symptoms) to 64 (most severe depression).

Secondary Outcome Measures

Montgomery Asberg Depression Rating Scale (MADRS)
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).

Full Information

First Posted
March 16, 2006
Last Updated
November 17, 2010
Sponsor
Mclean Hospital
Collaborators
Solvay Pharmaceuticals
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1. Study Identification

Unique Protocol Identification Number
NCT00304746
Brief Title
AndroGel in Men With Major Depression and Incomplete Response to Antidepressant Treatment
Official Title
A Parallel-Group, Placebo-Controlled Trial of AndroGel in Men With Major Depressive Disorder Who Display an Incomplete Response to Standard Antidepressant Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
November 2010
Overall Recruitment Status
Completed
Study Start Date
April 2006 (undefined)
Primary Completion Date
December 2008 (Actual)
Study Completion Date
April 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Mclean Hospital
Collaborators
Solvay Pharmaceuticals

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depressive Disorder, Major

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
testosterone gel
Arm Type
Active Comparator
Arm Description
AndroGel (1% testosterone transdermal gel), 2.5 g to 10 g daily
Arm Title
placebo gel
Arm Type
Placebo Comparator
Arm Description
Placebo gel
Intervention Type
Drug
Intervention Name(s)
Testosterone gel
Other Intervention Name(s)
AndroGel
Intervention Description
AndroGel 2.5g and 5g sachets at doses ranging from 10g/day for duration of trial.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
21-item Hamilton Depression Rating Scale Score (HAM-D)
Description
The HAM-D generates a score ranging from 0 (no depressive symptoms) to 64 (most severe depression).
Time Frame
9 weeks (1-week placebo lead-in and 8 weeks of blinded medication treatment)
Secondary Outcome Measure Information:
Title
Montgomery Asberg Depression Rating Scale (MADRS)
Description
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).
Time Frame
9 weeks (1 week of placebo lead-in and 8 weeks of blinded medication treatment)

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Harrison G Pope, M.D.
Organizational Affiliation
Mclean Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Stuart N Seidman, M.D.
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
McLean Hospital
City
Belmont
State/Province
Massachusetts
ZIP/Postal Code
02478
Country
United States
Facility Name
The Chaim Sheba Medical Center
City
Tel-Hashomer
ZIP/Postal Code
52621
Country
Israel

12. IPD Sharing Statement

Citations:
PubMed Identifier
20520285
Citation
Pope HG Jr, Amiaz R, Brennan BP, Orr G, Weiser M, Kelly JF, Kanayama G, Siegel A, Hudson JI, Seidman SN. Parallel-group placebo-controlled trial of testosterone gel in men with major depressive disorder displaying an incomplete response to standard antidepressant treatment. J Clin Psychopharmacol. 2010 Apr;30(2):126-34. doi: 10.1097/JCP.0b013e3181d207ca.
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AndroGel in Men With Major Depression and Incomplete Response to Antidepressant Treatment

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