Treatment of Depression in Youth With Bipolar Disorders
Information source: National Institute of Mental Health (NIMH)
Information obtained from ClinicalTrials.gov on June 20, 2008 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Bipolar Disorder; Depression
Intervention: Fluoxetine (Drug)
Phase: Phase 3
Status: Terminated
Sponsored by: National Institute of Mental Health (NIMH)
Summary
THIS STUDY HAS BEEN DISCONTINUED.
The study is designed to evaluate the safety and efficacy of fluoxetine for treating children
and adolescents with Bipolar Disorder who are experiencing an episode of major depression
while being treated with a mood stabilizer. The study involves a 2-week assessment period.
Patients who are on stable, therapeutic doses of lithium or valproate and continue to have
depression will be randomized to a 12-week treatment of fluoxetine or placebo. Those who
respond favorably to treatment will be followed openly for an 18-week continuation phase.
Clinical Details
Official title: Fluoxetine for the Treatment of Major Depression in Youth With Bipolar Disorder _
Study design: Treatment, Double-Blind, Placebo Control
Detailed description:
This NIMH sponsored study is being done to determine the safety and efficacy of a selective
serotonin reuptake inhibitor (SSRI), fluoxetine (Prozac), compared to placebo in the
treatment of children and adolescents with bipolar disorder who, while taking a mood
stabilizer, are currently experiencing an episode of major depression. Bipolar disorder is a
recurrent, episodic illness with key features of severe mood swings from one extreme
(depression) to the other extreme (mania). These mood swings and associated symptoms are not
similar to the normal mood changes that individuals experience from time to time. A person
suffering from bipolar disorder, while in an episode of depression or mania, experiences
problems in their functioning in several different areas in his or her life such as
interpersonal, social, academic and occupational. Symptoms of depression include sad or
irritable mood, sleep and appetite disturbances, trouble concentrating, inability to enjoy
things that are normally fun, feelings of guilt, low self-esteem, withdrawal from family and
friends, suicidal ideation. Symptoms of mania include extremely happy or irritable mood,
little need for sleep, poor judgment, continuous high energy, overconfidence, racing
thoughts, increase in social interactions, frequent or constant thoughts about sex. There are
varying degrees and types of bipolar disorder.
Pediatric bipolar disorder is now recognized as a significant health problem. Studies of
adults have shown that approximately 40% of bipolar patients started to suffer from this
disorder during their teens. Bipolar disorder is usually treated with medications, such as
lithium or valproate (Depakote), to stabilize the mood swings. Sometimes people with bipolar
disorder experience depression, even when they are taking a mood stabilizer medication. When
this happens, an antidepressant medication may need to be added to treat the depressive
symptoms. The current practice for treatment of bipolar disorder in children and adolescents
in the depressed phase follows treatment guidelines developed for adults, but it is unknown
whether these treatment strategies are appropriate for children and teens. Few studies have
been done in youth.
Fluoxetine has been approved by the Food and Drug Administration (FDA) for treatment of
depression, bulimia, and obsessive-compulsive disorder in adults, but not in children or
adolescents. Previous research has shown that fluoxetine is an effective treatment for
periods of depression, however, in this study the investigators are evaluating whether it is
effective for periods of depression associated with bipolar disorders. In this study, about
100 children and adolescents (ages 8-18 years) who are taking lithium carbonate or valproate
(Depakote) and are experiencing depression will be randomized to receive fluoxetine (Prozac)
or placebo for 12 weeks. Weekly visits to the clinic are necessary for participation to
ensure safety. At the end of the 12 weeks there is an 18-week open treatment period, which
will involve clinic visits at least monthly. Those who were taking fluoxetine and improved
will continue taking the fluoxetine during this time period. Those who did not improve will
either receive an increased dose of fluoxetine or will be assigned to a different medication.
Those who were taking placebo and did not improve will be offered treatment with fluoxetine
and those who improved with placebo will continue taking only lithium or valproate.
Eligibility
Minimum age: 8 Years.
Maximum age: 18 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Inclusion Criteria:
- Free of manic symptoms for at least 4 weeks. Must be treated with valproate or lithium
(mood stabilizers) for at least 4 weeks. Meet criteria for major depression and
bipolar disorder (BP-I, BP-II, or BP-NOS). Not pregnant
Exclusion Criteria:
- Exclusion Criteria:
- Patients with schizophrenia, autism, schizoaffective disorder, organic mood disorder,
obsessive-compulsive disorder, eating disorder, and psychosis. IQ less than 70.
Significant chronic medical illness such as diabetes, epilepsy. Pregnancy. Substance
abuse in last 3 months. Concurrent psychotherapy. Previous lack of response to
adequate treatment with fluoxetine or other SSRI. Current use of psychoactive
medication other than lithium or valproate.
Locations and Contacts
Additional Information
Ending date: September 2000
Last updated: November 17, 2005
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