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Phase 3 N=16 Treatment

The Combination of Aripiprazole and Antidepressants in Psychotic Major Depression

Psychotic Depression

Enrolled (actual)
16
Serious AEs
12.5%
Results posted
Aug 2012
Primary outcome: Primary: Depression and Psychosis Response Rate — 62.5 percent of participants

Study Design & Population

Study type
Interventional
Phase
Phase 3
Interventions
Aripiprazole (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Massachusetts General Hospital
Primary completion
Jan 2008

Outcome Measures

OutcomeResultp-value
PRIMARY
Depression and Psychosis Response Rate
62.5
SECONDARY
Depression and Psychosis Remission Rate
50

Summary

The purpose of the study is to assess the safety and effectiveness of the combination of aripiprazole (Abilify) and selective serotonin reuptake inhibitors (SSRIs) in subjects with psychotic major depression.

Eligibility Criteria

Inclusion Criteria

  • Men and women aged 18-80 years, inclusive.
  • Drug-free outpatients or inpatients meeting DSM-IV criteria for major depression with psychotic features.
  • Inpatients who undergo a 5-7 day washout period of their medication while concurrently beginning one of the approved SSRI's and abilify.
  • HAM-D-24 score > 16.

Exclusion Criteria

  • Pregnant women and women of child bearing potential not using a medically accepted means of contraception (oral contraceptives are allowed).
  • Women who are breast-feeding.
  • Patients meeting DSM-IV criteria for major depression without psychotic features, or psychosis without major depression at the screen visit.
  • Patients with serious suicidal risk.
  • Patients with a history of seizure disorder; unstable physical disorders (cardiovascular, hepatic, renal, respiratory, endocrine, neurologic, or hematologic); or any physical disorder judged to significantly affect central nervous system function.
  • Patients meeting criteria for the following DSM-IV diagnoses: organic mental disorders; substance use disorders, including alcohol, active within the last 6 months; bipolar disorder; schizoaffective disorder; or antisocial personality disorder.
  • Patients who are currently taking an antidepressant, antipsychotic, or mood stabilizing drug and who are responding to one or all of these medications. If patients are not responding to these medications, they may go through a washout period of at least one week under the supervision of a study doctor before entering into this study.
  • Patients who are not able to read and understand the consent form, or who are not capable of understanding or giving informed consent to the procedures of the study
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00556140). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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