Schizophrenia Clinical Trial
Official title:
A Randomized, Rater-Blind, Controlled, Clinical Trial of Conversion to Antipsychotic Monotherapy vs. Continued Polypharmacy for Patients With Schizophrenia or Schizoaffective Disorder
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.
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.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05039489 -
A Study on the Brain Mechanism of cTBS in Improving Medication-resistant Auditory Hallucinations in Schizophrenia
|
N/A | |
Completed |
NCT05321602 -
Study to Evaluate the PK Profiles of LY03010 in Patients With Schizophrenia or Schizoaffective Disorder
|
Phase 1 | |
Completed |
NCT05111548 -
Brain Stimulation and Cognitive Training - Efficacy
|
N/A | |
Completed |
NCT04503954 -
Efficacy of Chronic Disease Self-management Program in People With Schizophrenia
|
N/A | |
Completed |
NCT02831231 -
Pilot Study Comparing Effects of Xanomeline Alone to Xanomeline Plus Trospium
|
Phase 1 | |
Completed |
NCT05517460 -
The Efficacy of Auricular Acupressure on Improving Constipation Among Residents in Community Rehabilitation Center
|
N/A | |
Completed |
NCT03652974 -
Disturbance of Plasma Cytokine Parameters in Clozapine-Resistant Treatment-Refractory Schizophrenia (CTRS) and Their Association With Combination Therapy
|
Phase 4 | |
Recruiting |
NCT04012684 -
rTMS on Mismatch Negativity of Schizophrenia
|
N/A | |
Recruiting |
NCT04481217 -
Cognitive Factors Mediating the Relationship Between Childhood Trauma and Auditory Hallucinations in Schizophrenia
|
N/A | |
Completed |
NCT00212784 -
Efficacy and Safety of Asenapine Using an Active Control in Subjects With Schizophrenia or Schizoaffective Disorder (25517)(P05935)
|
Phase 3 | |
Completed |
NCT04092686 -
A Clinical Trial That Will Study the Efficacy and Safety of an Investigational Drug in Acutely Psychotic People With Schizophrenia
|
Phase 3 | |
Completed |
NCT01914393 -
Pediatric Open-Label Extension Study
|
Phase 3 | |
Recruiting |
NCT03790345 -
Vitamin B6 and B12 in the Treatment of Movement Disorders Induced by Antipsychotics
|
Phase 2/Phase 3 | |
Recruiting |
NCT05956327 -
Insight Into Hippocampal Neuroplasticity in Schizophrenia by Investigating Molecular Pathways During Physical Training
|
N/A | |
Terminated |
NCT03261817 -
A Controlled Study With Remote Web-based Adapted Physical Activity (e-APA) in Psychotic Disorders
|
N/A | |
Terminated |
NCT03209778 -
Involuntary Memories Investigation in Schizophrenia
|
N/A | |
Completed |
NCT02905604 -
Magnetic Stimulation of the Brain in Schizophrenia or Depression
|
N/A | |
Recruiting |
NCT05542212 -
Intra-cortical Inhibition and Cognitive Deficits in Schizophrenia
|
N/A | |
Completed |
NCT04411979 -
Effects of 12 Weeks Walking on Cognitive Function in Schizophrenia
|
N/A | |
Terminated |
NCT03220438 -
TMS Enhancement of Visual Plasticity in Schizophrenia
|
N/A |