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Antidepressant Therapy for Bipolar II Major Depression

Primary Purpose

Bipolar Type II Disorder

Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Venlafaxine
Lithium Carbonate
Sponsored by
Stanley Medical Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bipolar Type II Disorder focused on measuring bipolar disorder, bipolar type II disorder, antidepressant, mood stabilizer, venlafaxine, lithium carbonate

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • men and women (all races and ethnicity) greater than or equal to18 years of age,
  • DSM IV diagnosis of BP II disorder,
  • Current DSM IV MDE,
  • HAM-D17 score greater than or equal to 16,
  • Drug free from prior psychotropic medication greater than or equal to 7 days (2 weeks for MAOIs)

Exclusion Criteria:

  • History of mania,
  • Other primary DSM IV Axis I diagnosis,
  • Alcohol or drug dependence within 3 months,
  • History of nonresponse to Effexor-XR or lithium in the present MDE,
  • History of allergic reaction to Effexor-XR or lithium,
  • Medical contraindications to treatment with Effexor-XR or lithium,
  • Unstable medical condition,
  • Pregnant or breast-feeding women,
  • Women of child-bearing potential not using a medically approved form of contraception,
  • Actively suicidal or requiring hospitalization,
  • Requiring concurrent antidepressant, neuroleptic or mood stabilizer therapy,
  • Prior investigational study within 4 weeks of starting active therapy.

Sites / Locations

  • Depression Research Unit, Department of Psychiatry, University of Pennsylvania

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

Antidepressant

Drug

Outcomes

Primary Outcome Measures

Reduction in Hamilton Depression Rating Scale score.

Secondary Outcome Measures

Change in Young Mania Rating Scale score.

Full Information

First Posted
March 18, 2008
Last Updated
March 18, 2008
Sponsor
Stanley Medical Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT00641927
Brief Title
Antidepressant Therapy for Bipolar II Major Depression
Official Title
Acute Antidepressant Therapy in Bipolar II Major Depression
Study Type
Interventional

2. Study Status

Record Verification Date
March 2008
Overall Recruitment Status
Completed
Study Start Date
April 2002 (undefined)
Primary Completion Date
October 2006 (Actual)
Study Completion Date
October 2006 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Stanley Medical Research Institute

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study examines the relative safety and benefit of antidepressant therapy (versus recommended mood stabilizer therapy)of bipolar type II major depressive episode. We hypothesize that antidepressant therapy will be superior to mood stabilizer therapy with little or no difference in treatment emergent manic symptoms.
Detailed Description
Bipolar type II (BP II) major depressive episode (MDE), affects 2.5% of the US adult population and results in an estimated healthcare cost of $40 billion annually. BP II disorder is a distinct clinical entity that differs from BP I disorder, and is characterized by a preponderance of MDEs that result in particularly high morbidity and mortality rates. The treatment of BP II MDE remains a challenge for clinicians. Concerns over antidepressant drug (AD) induced manic switch episodes have led current practice guidelines to recommend treating BP II MDE with mood stabilizer (MS) monotherapy and to avoid AD monotherapy. To date, there are no controlled clinical trials to test the validity of these empirical guidelines. Results from our preliminary BP II MDE studies have shown that fluoxetine monotherapy may be safe and effective initial treatment of BP II MDE with a low manic switch rate. Based upon these observations, we now ask (Specific aim #1): "What is the relative safety and efficacy of initial AD monotherapy vs. MS monotherapy of BP II MDE?" and "What is the relative manic switch rate of initial AD vs. MS monotherapy of BP II MDE?" To answer these questions, patients with BP II MDE will be treated in a 12-week, randomized, parallel group comparison of venlafaxine monotherapy vs. lithium monotherapy. We hypothesize that AD monotherapy will have superior efficacy vs. MS monotherapy, and that there will be a similar manic switch rate among both treatment conditions. If our hypotheses are correct, we believe that these results may have an important public health impact on the current practice guidelines for treating BP II MDE.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bipolar Type II Disorder
Keywords
bipolar disorder, bipolar type II disorder, antidepressant, mood stabilizer, venlafaxine, lithium carbonate

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
90 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Antidepressant
Arm Title
2
Arm Type
Active Comparator
Arm Description
Drug
Intervention Type
Drug
Intervention Name(s)
Venlafaxine
Other Intervention Name(s)
Effexor-XR
Intervention Description
37.5 mg - 375 mg daily, 12 Weeks
Intervention Type
Drug
Intervention Name(s)
Lithium Carbonate
Other Intervention Name(s)
Lithium
Intervention Description
300 mg - 2100 mg daily, 12 weeks
Primary Outcome Measure Information:
Title
Reduction in Hamilton Depression Rating Scale score.
Time Frame
12 Weeks
Secondary Outcome Measure Information:
Title
Change in Young Mania Rating Scale score.
Time Frame
12 Weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: men and women (all races and ethnicity) greater than or equal to18 years of age, DSM IV diagnosis of BP II disorder, Current DSM IV MDE, HAM-D17 score greater than or equal to 16, Drug free from prior psychotropic medication greater than or equal to 7 days (2 weeks for MAOIs) Exclusion Criteria: History of mania, Other primary DSM IV Axis I diagnosis, Alcohol or drug dependence within 3 months, History of nonresponse to Effexor-XR or lithium in the present MDE, History of allergic reaction to Effexor-XR or lithium, Medical contraindications to treatment with Effexor-XR or lithium, Unstable medical condition, Pregnant or breast-feeding women, Women of child-bearing potential not using a medically approved form of contraception, Actively suicidal or requiring hospitalization, Requiring concurrent antidepressant, neuroleptic or mood stabilizer therapy, Prior investigational study within 4 weeks of starting active therapy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jay D Amsterdam, MD
Organizational Affiliation
Depression Research Unit, School of Psychiatry, University of Pennsylvania
Official's Role
Principal Investigator
Facility Information:
Facility Name
Depression Research Unit, Department of Psychiatry, University of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104-3309
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
19472307
Citation
Shults J, Sun W, Tu X, Kim H, Amsterdam J, Hilbe JM, Ten-Have T. A comparison of several approaches for choosing between working correlation structures in generalized estimating equation analysis of longitudinal binary data. Stat Med. 2009 Aug 15;28(18):2338-55. doi: 10.1002/sim.3622.
Results Reference
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Antidepressant Therapy for Bipolar II Major Depression

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