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TerminatedNCT01368458MOPEUpdated Feb 9, 2017

Conversion to Antipsychotic Monotherapy

An interventional study of Conversion to Antipsychotic Monotherapy in Schizophrenia and Schizoaffective Disorder, sponsored by Nathan Kline Institute for Psychiatric Research. Terminated. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2017-02-09.

Sponsored by Nathan Kline Institute for Psychiatric Research · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
24
Allocation
Randomized
Ages
18 Years to 75 Years
Sex
All
01

Study summary

This is a 12-week, with a 32-week follow-up, rater-blind, randomized controlled trial to determine whether patients with chronic schizophrenia or schizoaffective disorder receiving two different antipsychotics simultaneously will have any significant change in psychopathology following conversion to antipsychotic monotherapy. Additionally, the effects of conversion to antipsychotic monotherapy will be assessed by neurocognitive tests.

The study will be conducted at the Clinical Research and Evaluation Facility (CREF), a specialized research unit jointly operated by the Nathan S Kline Institute for Psychiatric Research (NKI) and Rockland Psychiatric Center (RPC). Patients will be recruited from the regular in-patient units of RPC and transferred to the CREF. Following baseline assessments, patients will be randomized to continued antipsychotic polypharmacy treatment or to systematic conversion to monotherapy.

Conversion to antipsychotic monotherapy will be assessed across multiple domains of psychopathology using the Positive and Negative Symptom Scale (PANSS). The primary outcome measure is PANSS total score. The secondary outcome measure is time on medication (all-cause dropouts). Mixed Model Repeated Measures (MMRM) will test the hypothesis that conversion to antipsychotic monotherapy will show minimal change from the control group.

Read the detailed description

Background:

Often, treatment resistant schizophrenia patients are treated with high doses of, or polypharmacy with, antipsychotics, or both. There is a lack of systematic evidence for either practice, and this is not recommended by most treatment guidelines. Often polypharmacy results in dosages well above the recommended upper limit of dosage. Recent studies of antipsychotic utilization, have reported that approximately 10-60% of patients are prescribed at least two antipsychotics.

Moreover, antipsychotic treatment carries substantial risks, including the potential development of tardive dyskinesia or metabolic syndrome. Higher doses may expose patients to more adverse events or consequences without any additional therapeutic benefit. Clear benefits of long-term treatment with antipsychotic polypharmacy have rarely been reported, and there is a void of long term double blind, placebo controlled trials.

Antipsychotic polypharmacy remains common, including patients receiving atypical antipsychotics. To our knowledge, no one has published a study of a systematic, randomized controlled conversion to antipsychotic monotherapy for patients with chronic schizophrenia or schizoaffective disorder receiving atypical antipsychotic polypharmacy.

Design:

Hospitalized patients with DSM-IV-TR schizophrenia or schizoaffective disorder meeting the following criteria: (1) at least two antipsychotics, (2) stable dosages for at least one month prior to baseline, (3) baseline dosages of at least one of the antipsychotics are at least olanzapine 15 mg, ziprasidone 120 mg, quetiapine 500 mg, risperidone 4 mg, aripiprazole 10 mg, paliperidone 6 mg, any dose of clozapine, or any first generation antipsychotic >300 chlorpromazine equivalents.

After a baseline assessment, patients will be randomized to conversion to antipsychotic monotherapy of one of their two antipsychotics or continued on their combination antipsychotic treatment. Other psychotropics will be left unchanged from baseline, and the prescription of a new psychotropic will not be permitted, excepting lorazepam and benztropine as detailed below.

If a patient is randomized to conversion to monotherapy, then the decision of which of the two baseline antipsychotics to continue will occur as follows:

  1. If one is clozapine, then clozapine will be continued.
  2. In all other cases:

    1. If only one of the antipsychotics is at a dose greater than the above noted doses, then that is one that will be continued.
    2. If both doses are greater than the above noted doses, then there will be a flip of a coin to determine which to continue, with heads equal the one with the higher alphabetic letter and tails equal to the lower.
02

Conditions studied

  • Schizophrenia
  • Schizoaffective Disorder
03

In context

Schizophrenia

3,471 studies on the registry are indexed under Schizophrenia; 471 are open to participants now.

This study's planned enrollment of 24 is below the median of 70 across 2,871 interventional studies indexed under Schizophrenia.

Browse Schizophrenia studies →

Lead sponsor

Nathan Kline Institute for Psychiatric Research is the lead sponsor of 22 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients aged 18-64 with a SCID DSM-IV-TR diagnosis of schizophrenia or schizoaffective disorder, confirmed by SCID, who are able to give written informed consent and on stable dosages of two antipsychotics for at least one month prior to baseline.

Exclusion criteria

Exclusion Criteria:

  • Lack of capacity to give informed consent (capacity is determined by a licensed member of the treatment team)
  • unstable medical illness
  • use of long acting injectable preparations of antipsychotic medication in the previous two months
  • documented failure of previous dose reduction
  • current treatment with clozapine
  • addition of any new psychotropic in the previous month
  • patients who are severely assaultive and in clinical need of more than one antipsychotic for their safe management
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
24 participants (estimated)

Study arms

  • Experimental
    Conversion to mono therapy

    Conversion from 2 to 1 antipsychotic

    Other: Conversion to Antipsychotic Monotherapy

  • No intervention
    control

    No change in antipsychotics

Interventions

  • OtherConversion to Antipsychotic Monotherapy

    Patients assigned to the antipsychotic monotherapy group will have the dosage of their secondary (i.e. one due to be reduced) antipsychotic reduced by decreased by approximately 1/3 every 3 weeks. Dosage of the primary antipsychotic will be left unchanged.

06

What researchers measure

Primary outcomes

  1. Positive and Negative Symptom Scale (PANSS) total score

    Time frame: 12 weeks

  2. Relapse Rate

    Time frame: 12 weeks

Secondary outcomes

  1. Nurses Observation Scale for Inpatient Evaluation (NOSIE)

    Time frame: 12 weeks

  2. Abnormal Involuntary Movement Scale (AIMS)

    Time frame: 12 weeks

  3. Simpson-Angus Scale (SAS)

    Time frame: 12 weeks

  4. Barnes Akathisia Scale

    Time frame: 12 weeks

  5. MATRICS

    Time frame: 12 weeks

  6. Clinical Global Impression (CGI)

    Time frame: 12 weeks

  7. Weight

    Time frame: 12 weeks

  8. Calgary Depression Scale for Schizophrenia (CDSS)

    Time frame: 12 weeks

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 9, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01368458
Lead sponsor
Nathan Kline Institute for Psychiatric Research
First posted
Jun 8, 2011
Start date
Dec 2007
Completion
Jul 2008
Last update
Feb 9, 2017

Study contacts

Joshua Kantrowitz, MD
principal investigator · Nathan Kline Institute

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Feb 2017. You cannot join it, but the record below documents what was studied.

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