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Completed

NCT Number: NCT00000385

Long-Term Lithium Treatment for Aggressive Conduct Disorder

This study will examine the long-term effects of lithium used to treat children and adolescents with aggressive conduct disorder (severe aggression).

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Key information

Age range

9 year–17 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Drexel University College of Medicine at Friends Hospital

Philadelphia, Pennsylvania, 19124, United States

About this study

Psychotherapeutic agents are often administered without sufficient testing to children and adolescents, often on a long-term basis, to reduce aggression. Many pressures, including managed care, will increase the utilization of pharmacotherapy in the outpatient setting to treat serious problems. Lithium is the most promising agent for the treatment of aggression in children and adolescents. However, it has not been shown that lithium is an effective treatment for these patients in the outpatient (non-hospital) setting, or on a long-term basis. The purpose of this study is to examine the long-term effects of lithium used to treat children and adolescents with aggressive conduct disorder (severe aggression).

The proposed study is a two-phased clinical trial of lithium for the treatment of aggression in conduct disorder. Both phases are double-blind and placebo-controlled with randomization and employ a parallel groups design. Phase 1 contains a short-term 8-week controlled trial, with twice as many subjects randomized to lithium as placebo, increasing the pool of potential lithium responders to continue to Phase 2. In Phase 2, lithium responders from Phase 1 enter a 6-month long-term controlled trial. Every attempt is made to define responders to lithium.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Males and females
  • Ages between 9 and 17 years.
  • Conduct disorder according to DSM-IV (As rated on the DICA-IV).
  • The aggression criterion at screening

Exclusion criteria

  • Mental Retardation.
  • Pervasive Developmental Disorder(s).
  • Major Depressive Disorder or Dysthymic Disorder.
  • Bipolar Disorder.
  • Psychotic Disorder (including Schizophreniform Disorder and Schizophrenia).
  • Major medical problem such as cardiac, renal, and thyroid diseases, or seizure disorder.
  • History of psychoactive medication in the previous 2 weeks.
  • Current Pregnancy in females.
  • History of Substance Dependence in the past month.
  • Prior to the proposed study, a history of lithium treatment with serum lithium levels of 0.4 mEq/L or higher for a cumulative period of greater than 10 days.

Treatment and study plan

Lithium

Drug

Lithium 600 mg to 2700 mg per day

Placebo

Drug

Matching placebo

Primary outcomes

  1. Overt Aggression Scale-Modified

    Time frame: Weekly in short term phase, Monthly in long-term phase

  2. Clinical Global Impressions-Improvement Item

    Time frame: Weekly in short term phase, Monthly in long-term phase

Secondary outcomes

  1. Children's Psychiatric Rating Scale-Selected Items

    Time frame: Weekly in short term phase, Monthly in long-term phase

  2. IOWA

    Time frame: Weekly in short term phase, Monthly in long-term phase

  3. DOTES

    Time frame: Weekly in short term phase, Monthly in long-term phase

  4. TESS

    Time frame: Weekly in short term phase, Monthly in long-term phase

Sponsors and collaborators

Lead sponsor

Drexel University

Other

Collaborators

  • National Institute of Mental Health (NIMH)

Registry information

Official study title

Long-Term Lithium for Aggressive Conduct Disorder

Important dates

Study start
1997
Primary completion
2003
Study completion
2005
First posted
Nov 3, 1999
Registry last updated
Nov 26, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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