search
Back to results

Desvenlafaxine Succinate (DVS) for Major Depressive Disorder (MDD) in Midlife Men and Women (DVS)

Primary Purpose

Major Depressive Disorder, Menopausal Staging and Vasomotor Symptoms (for Females)

Status
Unknown status
Phase
Phase 3
Locations
Canada
Study Type
Interventional
Intervention
Desvenlafaxine Succinate
Sponsored by
Hamilton Health Sciences Corporation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Major Depressive Disorder focused on measuring depression, desvenlafaxine, menopause, imaging, FMRI

Eligibility Criteria

40 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • men and women, aged 40-60 years
  • diagnosis of MDD
  • for women, perimenopausal or postmenopausal

Exclusion Criteria:

  • other DSM-IV axis I diagnosis other than MDD
  • using psychotropic medications
  • suicidal ideation, homicidal ideation, or psychotic symptoms
  • presence of laboratory abnormalities at baseline visit
  • presence of heart disease, liver disease, kidney disease, pulmonary disease, blood or bleeding disease, thyroid disease, GI disease, seizure or epilepsy, head injury, cancer, uterine fibroids or endometriosis, gynecologic surgeries (except caesarian sections), electroconvulsive therapies in the past 3 months, HIV+/AIDS
  • in addition (for women): use of hormone replacement therapies, menstrual dysfunction, pregnancy or breastfeeding

Sites / Locations

  • Women's Health Concerns ClinicRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

A

Arm Description

Use of desvenlafaxine succinate, flexible dose (50-100mg/day)

Outcomes

Primary Outcome Measures

Effects of desvenlafaxine succinate (DVS) on brain structure and activation in midlife men and women with MDD.

Secondary Outcome Measures

Changes in brain activity
Changes in menopause-related symptoms among females

Full Information

First Posted
April 27, 2009
Last Updated
February 7, 2012
Sponsor
Hamilton Health Sciences Corporation
Collaborators
Wyeth is now a wholly owned subsidiary of Pfizer, St. Joseph's Healthcare Hamilton, McMaster University
search

1. Study Identification

Unique Protocol Identification Number
NCT00888862
Brief Title
Desvenlafaxine Succinate (DVS) for Major Depressive Disorder (MDD) in Midlife Men and Women
Acronym
DVS
Official Title
Desvenlafaxine Succinate in Major Depressive Disorder: Effects on Structural and Functional Imaging, Cognition, and Functional Outcomes in Midlife Women and Men
Study Type
Interventional

2. Study Status

Record Verification Date
April 2009
Overall Recruitment Status
Unknown status
Study Start Date
June 2009 (undefined)
Primary Completion Date
June 2012 (Anticipated)
Study Completion Date
October 2012 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hamilton Health Sciences Corporation
Collaborators
Wyeth is now a wholly owned subsidiary of Pfizer, St. Joseph's Healthcare Hamilton, McMaster University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The main objective of this study is to characterize a range of brain activation symptoms associated with depression and response to treatment in midlife men and women with MDD, using MRI and functional MRI. Moreover, in the female sub-group, the investigators will examine whether these brain activation symptoms are related to menopausal symptoms (i.e., hot flashes and night sweats). Also, assessing brain activation before and after the treatment might help to uncover some mechanisms associated with the pathophysiology of depression and menopause.
Detailed Description
Major Depressive Disorder (MDD) has been associated with morphological changes in the brain and changes in key brain areas. Studies have shown that antidepressant use may promote the normalization of these areas. Moreover, midlife men and women appear to be at greater risk for developing major depressive episodes. In women, this period of life has been associated with significant functional impairment due to the presence/severity of vasomotor symptoms (hot flashes, night sweats), cognitive complaints, and poorer quality of life. Desvenlafaxine succinate (DVS) has been developed for the treatment of MDD. To date, the effects of DVS on brain structure and functioning in midlife men and women with MDD, as well as on depression related to menopause, has not been explored. The present study aims to investigate the effects of DVS on brain structure and functioning when used for the treatment of a major depressive episode in midlife men and women, using MRI and functional MRI. In addition, the investigators will examine whether the impact of treatment with DVS on vasomotor symptoms, cognition, and quality of life modulate the putative changes in brain structure and functioning.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depressive Disorder, Menopausal Staging and Vasomotor Symptoms (for Females)
Keywords
depression, desvenlafaxine, menopause, imaging, FMRI

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
90 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Experimental
Arm Description
Use of desvenlafaxine succinate, flexible dose (50-100mg/day)
Intervention Type
Drug
Intervention Name(s)
Desvenlafaxine Succinate
Other Intervention Name(s)
Pristiq
Intervention Description
Desvenlafaxine Succinate, 50-100mg/day for 8 weeks
Primary Outcome Measure Information:
Title
Effects of desvenlafaxine succinate (DVS) on brain structure and activation in midlife men and women with MDD.
Time Frame
10 weeks
Secondary Outcome Measure Information:
Title
Changes in brain activity
Time Frame
10 weeks
Title
Changes in menopause-related symptoms among females
Time Frame
10 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: men and women, aged 40-60 years diagnosis of MDD for women, perimenopausal or postmenopausal Exclusion Criteria: other DSM-IV axis I diagnosis other than MDD using psychotropic medications suicidal ideation, homicidal ideation, or psychotic symptoms presence of laboratory abnormalities at baseline visit presence of heart disease, liver disease, kidney disease, pulmonary disease, blood or bleeding disease, thyroid disease, GI disease, seizure or epilepsy, head injury, cancer, uterine fibroids or endometriosis, gynecologic surgeries (except caesarian sections), electroconvulsive therapies in the past 3 months, HIV+/AIDS in addition (for women): use of hormone replacement therapies, menstrual dysfunction, pregnancy or breastfeeding
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Stefanie M Attard
Phone
905-522-1155
Ext
32048
Email
sattard@stjoes.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Benicio N Frey, MD, PhD
Phone
905-522-1155
Ext
35123
Email
freybn@mcmaster.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Claudio N Soares, MD, PhD
Organizational Affiliation
St. Joseph's Healtcare; McMaster University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Women's Health Concerns Clinic
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8P 3B6
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stefanie M Attard
Phone
905-522-1155
Ext
32048
Email
sattard@stjoes.ca
First Name & Middle Initial & Last Name & Degree
Claudio N Soares, MD, PhD
First Name & Middle Initial & Last Name & Degree
Benicio N Frey, MD, PhD
First Name & Middle Initial & Last Name & Degree
Geoff Hall, PhD
First Name & Middle Initial & Last Name & Degree
Meir Steiner, MD, PhD

12. IPD Sharing Statement

Citations:
PubMed Identifier
20616670
Citation
Frey BN, Hall GB, Attard S, Yucel K, Skelin I, Steiner M, Soares CN. Shift in the brain network of emotional regulation in midlife women: is the menopausal transition the turning point? Menopause. 2010 Jul;17(4):840-5. doi: 10.1097/gme.0b013e3181df840f.
Results Reference
result

Learn more about this trial

Desvenlafaxine Succinate (DVS) for Major Depressive Disorder (MDD) in Midlife Men and Women

We'll reach out to this number within 24 hrs