Bipolar II Depression: Lithium, SSRI, or the Combination

This study has been completed.
Sponsor:
Collaborators:
University of California, Los Angeles
Stanford University
Information provided by (Responsible Party):
Lindner Center of HOPE
ClinicalTrials.gov Identifier:
NCT00276965
First received: January 12, 2006
Last updated: May 8, 2013
Last verified: May 2013

January 12, 2006
May 8, 2013
September 2006
March 2012   (final data collection date for primary outcome measure)
Determine switch rate to Mania/hypomania [ Time Frame: Measured at week 16 ] [ Designated as safety issue: No ]
Not Provided
Complete list of historical versions of study NCT00276965 on ClinicalTrials.gov Archive Site
  • Side effects [ Time Frame: Measured at week 16 ] [ Designated as safety issue: No ]
  • Antidepressant response [ Time Frame: Measured at week 16 ] [ Designated as safety issue: No ]
  • Mood variability [ Time Frame: Measured at week 16 ] [ Designated as safety issue: No ]
Not Provided
Not Provided
Not Provided
 
Bipolar II Depression: Lithium, SSRI, or the Combination
Comparing the Safety and Effectiveness of a Mood Stabilizing Medication, an Antidepressant Medication, and a Combination of Both Medications to Treat Symptoms of Bipolar Type II Depression

This study will compare the safety and effectiveness of a mood stabilizing medication, an antidepressant medication, and a combination of both medications to treat symptoms of bipolar type II depression.

Bipolar type II depression (BD II) is a less severe type of bipolar disorder. BD II is characterized by one or more depressive episodes and at least one hypomanic episode. During hypomanic episodes, people experience especially energetic or anxious moods, and their thoughts are more sporadic than usual, but they do not experience the severity of mania. Symptoms of BD II are known to impair daily functioning as well as cause distress and even suicide. Antidepressant medication alone is not recommended for people with bipolar disorder because manic symptoms usually worsen. It is unknown whether the same recommendation should apply to people with BD II. Sertraline is a selective serotonin reuptake inhibitor (SSRI) antidepressant that increases levels of serotonin, helping the brain to maintain mental stability. It is often used to treat depression, panic attacks, and other disorders. Lithium is a mood stabilizing medication that decreases abnormal brain activity and is used to treat and prevent recurring episodes of mania in people with bipolar disorders. This study will evaluate the effectiveness of lithium alone, sertraline alone, and lithium with sertraline to treat symptoms of BD II.

Participation in this double-blind study will last up to 18 weeks. Participants will be randomly assigned to receive either lithium, sertraline, or lithium and sertraline. Both medications will initially be given at a low dose and then gradually increased over 2 weeks. For the remainder of the study, dosages will be adjusted as necessary. Study visits will occur every week for the first 6 weeks and then every other week for the remaining 10 weeks. During all study visits, participants will complete a psychiatric assessment and questionnaires about their current mood and any treatment side effects. Urine and blood collection may occur at selected times during the study.

Interventional
Phase 3
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator)
Primary Purpose: Treatment
  • Bipolar Disorder
  • Depression
  • Drug: Sertraline
    Sertraline or placebo for sertraline starting at 25 mg per day, up to maximum of 200 mg per day
    Other Name: Zoloft
  • Drug: Lithium carbonate
    Lithium or placebo for lithium starting at 150 mg per day; target dose of 900mg per day. Maximum dose based on clinical response and serum levels (maximum serum level of 1.2 mEq/L).
    Other Name: Eskalith, Lithobid
  • Experimental: A
    Participants will take lithium only.
    Intervention: Drug: Lithium carbonate
  • Experimental: B
    Participants will take lithium and sertraline.
    Interventions:
    • Drug: Sertraline
    • Drug: Lithium carbonate
  • Experimental: C
    Participants will take sertraline only.
    Intervention: Drug: Sertraline
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
139
July 2012
March 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Meets DSM-IV criteria for bipolar type II disorder by Structured Clinical Interview for DSM-IV (SCID)
  • Meets DSM-IV criteria for current depressive episode
  • Inventory of Depressive Symptomology (IDS-C) score greater than 22
  • Clinical Global Impression Scale for Bipolar Illness (CGI-BP) depression subscale score greater than 3 (mildly ill or greater) and mania subscale score of 1 (not ill)
  • Young Mania Rating Scale (YMRS) score less than 8
  • Willing to discontinue antidepressant medication
  • Considered stable and does not require adjustments in treatment for other conditions or illnesses
  • Willing to use an effective form of birth control throughout the study
  • Speaks English

Exclusion Criteria:

  • Pregnant or breastfeeding
  • Unsuccessfully treated for more than 6 weeks with sertraline or lithium for depression
  • Suicidal
  • Significant alcohol or substance abuse or dependence within 3 months of study entry
  • Diagnosed with Axis II borderline personality disorder
  • Psychotic
  • Organic mood disorder (e.g., head trauma or cerebrovascular accident preceding mood episode)
  • Active hepatitis, liver failure, or kidney failure
  • Creatinine greater than 1 mg/dL
  • Liver function tests greater than 3 times the upper limit of normal
  • Abnormal thyroid-stimulating hormone
  • Unstable medical condition
Both
18 Years to 65 Years
No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00276965
R01 MH074707, R01MH074707, DATR A5-ETMA
Yes
Lindner Center of HOPE
Lindner Center of HOPE
  • National Institute of Mental Health (NIMH)
  • University of California, Los Angeles
  • Stanford University
Principal Investigator: Lori Altshuler, MD UCLA Mood Disorders Research Program
Lindner Center of HOPE
May 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP