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Effectiveness of Aripiprazole for Improving Side Effects of Clozapine in the Treatment of People With Schizophrenia
This study is ongoing, but not recruiting participants.
First Received: June 23, 2006   Last Updated: February 3, 2009   History of Changes
Sponsored by: National Institute of Mental Health (NIMH)
Information provided by: National Institute of Mental Health (NIMH)
ClinicalTrials.gov Identifier: NCT00345033
  Purpose

This study will evaluate the effects of combination treatment with aripiprazole and clozapine on insulin resistance, blood fat levels, and weight gain in people with schizophrenia.


Condition Intervention Phase
Schizophrenia
Insulin Resistance
Drug: Aripiprazole
Drug: Placebo
Phase IV

MedlinePlus related topics: Schizophrenia
Drug Information available for: Aripiprazole Clozapine
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double Blind (Subject, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Efficacy Study
Official Title: Aripiprazole for Clozapine Associated Medical Morbidity

Further study details as provided by National Institute of Mental Health (NIMH):

Primary Outcome Measures:
  • Fasting lipids, including triglycerides and total cholesterol [ Time Frame: Measured at Week 12 ] [ Designated as safety issue: Yes ]
  • Weight [ Time Frame: Measured at Week 12 ] [ Designated as safety issue: Yes ]
  • Body Mass Index (BMI) [ Time Frame: Measured at Week 12 ] [ Designated as safety issue: Yes ]
  • Insulin resistance and glucose metabolism [ Time Frame: Measured at Week 12 ] [ Designated as safety issue: Yes ]

Secondary Outcome Measures:
  • Food intake [ Time Frame: Measured at Week 12 ] [ Designated as safety issue: Yes ]
  • Energy expenditure [ Time Frame: Measured at Week 12 ] [ Designated as safety issue: Yes ]
  • Systematic Assessment for Treatment Emergent Effects (SAFTEE) [ Time Frame: Measured at Week 12 ] [ Designated as safety issue: Yes ]
  • Vital signs [ Time Frame: Measured at Week 12 ] [ Designated as safety issue: Yes ]
  • Plasminogen activator molecule-1 (PAI-1) [ Time Frame: Measured at Week 12 ] [ Designated as safety issue: Yes ]
  • LDL particle size [ Time Frame: Measured at Week 12 ] [ Designated as safety issue: Yes ]
  • C-reactive protein [ Time Frame: Measured at Week 12 ] [ Designated as safety issue: Yes ]
  • Soluble intercellular adhesion molecule-1 [ Time Frame: Measured at Week 12 ] [ Designated as safety issue: Yes ]
  • Lipid abnormalities [ Time Frame: Measured at Week 12 ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 70
Study Start Date: March 2005
Estimated Study Completion Date: October 2009
Estimated Primary Completion Date: October 2008 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Experimental
Participants will take aripiprazole for 8 weeks.
Drug: Aripiprazole
15-mg dose once a day for 8 weeks
2: Placebo Comparator
Participants will take placebo for 8 weeks.
Drug: Placebo
15-mg dose once a day for 8 weeks

Detailed Description:

Schizophrenia is a severely disabling brain disorder. People with schizophrenia often experience hallucinations and delusions, as well as overall difficulty with everyday functioning. Although the medications available to treat the disorder are generally effective, many cause undesirable side effects. Clozapine, for example, is a strong tranquilizer that functions like an antipsychotic medication. It has been shown to be effective in reducing the symptoms of schizophrenia, but can bring about serious side effects, including heart failure, weight gain, and diabetes. Aripiprazole, an atypical antipsychotic medication, has been shown to have fewer side effects than older antipsychotic drugs. The addition of aripiprazole to a clozapine treatment regimen may reduce the negative side effects of clozapine. This study will evaluate the effects of combination treatment with aripiprazole and clozapine on insulin resistance, blood fat levels, and weight gain in people with schizophrenia.

Individuals interested in participating in this 12-week, double-blind study will first attend a screening session at the study site. Medical and psychiatric evaluations will be completed, blood samples will be taken, and an EKG will be performed. Eligible participants will undergo baseline assessments and then be randomly assigned to receive either aripiprazole or placebo in addition to their prescribed dose of clozapine. Participants will take one 15-mg capsule of their assigned medication once a day for 8 weeks. Study visits will occur biweekly for the first 8 weeks, followed by one final visit at Week 12. At each study visit, medication will be distributed, and the following criteria will be assessed: vital signs; weight; complete blood count; medication side effects; and extrapyramidal symptoms (EPS), which are potential neurological side effects of antipsychotic medications and may include involuntary movements, tremors, and rigidity. The Week 12 follow-up visit will include an EKG, and assessments of the following criteria: vital signs; medication side effects; treatment efficacy; blood counts; weight and height; and waist and hip circumference. At baseline and Week 12, participants will also undergo a frequently sampled intravenous glucose tolerance test (FSIVGTT). This involves intravenous infusion of glucose followed by frequent blood sampling to measure insulin and glucose concentrations. During the 4 days prior to each FSIVGTT, participants will record their food intake and wear an activity monitor.

  Eligibility

Ages Eligible for Study:   18 Years to 65 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Diagnosis of schizophrenia (any subtype) or schizoaffective disorder (any subtype)
  • Treatment with clozapine for at least 1 year
  • Stable dose of clozapine for at least 1 month
  • Well established compliance with outpatient medications
  • Female participants of non-childbearing potential or of childbearing potential and willing to practice appropriate birth control methods (complete abstinence from sexual intercourse, female sterilization, sterilization of male partner, implants of levonorgestrel, injectable progestogen, oral contraceptives, intrauterine devices, or double barrier methods of contraception using spermicide with either a condom or diaphragm) during the study

Exclusion Criteria:

  • Current substance abuse
  • Psychiatrically unstable
  • Significant medical illness, including severe cardiovascular, hepatic, or renal disease
  • History of immunosuppression
  • Current or recent radiation or chemotherapy treatment for cancer
  • Chronic use of steroids
  • Pregnant or breastfeeding
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00345033

Locations
United States, Massachusetts
Massachusetts General Hospital Schizophrenia Program
Boston, Massachusetts, United States, 02114
Sponsors and Collaborators
Investigators
Principal Investigator: David C. Henderson, MD Massachusetts General Hospital
  More Information

Publications:
Casey DE, Carson WH, Saha AR, Liebeskind A, Ali MW, Jody D, Ingenito GG; Aripiprazole Study Group. Switching patients to aripiprazole from other antipsychotic agents: a multicenter randomized study. Psychopharmacology (Berl). 2003 Apr;166(4):391-9. Epub 2003 Feb 28.
Goldstein LE, Sporn J, Brown S, Kim H, Finkelstein J, Gaffey GK, Sachs G, Stern TA. New-onset diabetes mellitus and diabetic ketoacidosis associated with olanzapine treatment. Psychosomatics. 1999 Sep-Oct;40(5):438-43. No abstract available.
Hadigan C, Miller K, Corcoran C, Anderson E, Basgoz N, Grinspoon S. Fasting hyperinsulinemia and changes in regional body composition in human immunodeficiency virus-infected women. J Clin Endocrinol Metab. 1999 Jun;84(6):1932-7.
Henderson DC, Cagliero E, Gray C, Nasrallah RA, Hayden DL, Schoenfeld DA, Goff DC. Clozapine, diabetes mellitus, weight gain, and lipid abnormalities: A five-year naturalistic study. Am J Psychiatry. 2000 Jun;157(6):975-81.
Marder SR, McQuade RD, Stock E, Kaplita S, Marcus R, Safferman AZ, Saha A, Ali M, Iwamoto T. Aripiprazole in the treatment of schizophrenia: safety and tolerability in short-term, placebo-controlled trials. Schizophr Res. 2003 Jun 1;61(2-3):123-36.
Visser M, Fuerst T, Lang T, Salamone L, Harris TB. Validity of fan-beam dual-energy X-ray absorptiometry for measuring fat-free mass and leg muscle mass. Health, Aging, and Body Composition Study--Dual-Energy X-ray Absorptiometry and Body Composition Working Group. J Appl Physiol. 1999 Oct;87(4):1513-20.
Wirshing DA, Boyd JA, Meng LR, Ballon JS, Marder SR, Wirshing WC. The effects of novel antipsychotics on glucose and lipid levels. J Clin Psychiatry. 2002 Oct;63(10):856-65.

Responsible Party: Massachusetts General Hospital Freedom Trail Clinic ( David C. Henderson, MD )
Study ID Numbers: R01 MH072635, DSIR 83-ATAP
Study First Received: June 23, 2006
Last Updated: February 3, 2009
ClinicalTrials.gov Identifier: NCT00345033     History of Changes
Health Authority: United States: Federal Government

Keywords provided by National Institute of Mental Health (NIMH):
Glucose Metabolism

Study placed in the following topic categories:
Metabolic Diseases
Tranquilizing Agents
Psychotropic Drugs
Central Nervous System Depressants
Antipsychotic Agents
Schizophrenia
Hyperinsulinism
Mental Disorders
Clozapine
Psychotic Disorders
Insulin Resistance
Aripiprazole
Glucose Metabolism Disorders
Metabolic Disorder
Schizophrenia and Disorders with Psychotic Features

Additional relevant MeSH terms:
Metabolic Diseases
Tranquilizing Agents
Physiological Effects of Drugs
Psychotropic Drugs
Central Nervous System Depressants
Antipsychotic Agents
Pharmacologic Actions
Schizophrenia
Hyperinsulinism
Mental Disorders
Therapeutic Uses
Insulin Resistance
Aripiprazole
Glucose Metabolism Disorders
Central Nervous System Agents
Schizophrenia and Disorders with Psychotic Features

ClinicalTrials.gov processed this record on May 07, 2009