Evidence map›Paper›PMID 16172203›Full record

Trial reportThe New England journal of medicine2005

Effectiveness of antipsychotic drugs in patients with chronic schizophrenia.

Jeffrey A Lieberman, T Scott Stroup, Joseph P McEvoy, Marvin S Swartz, Robert A Rosenheck, Diana O Perkins, Richard S E Keefe, Sonia M Davis, Clarence E Davis, Barry D Lebowitz and 3 more

Erratum issued 10 registry-linked trialsOpen access · bronzeAbstract readClinical TrialComparative StudyMulticenter Study
PubMed Publisher
In one paragraph

Trial report in The New England journal of medicine, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to 10 registered trials, which are not on this map. Cited by 1,716 papers, 11 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,716citing papers in PubMed, 11 pooled it
213.5field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT00014001 phase4completednot on this map

Comparative Effectiveness of Antipsychotic Medications in Patients With Schizophrenia (CATIE Schizophrenia Trial)

TypeinterventionalSponsorNational Institute of Mental Health (NIMH)Ran2000 to 2004Enrolled1,600ConditionsSchizophreniaArmsperphenazine, olanzapine, quetiapine, risperidone, ziprasidone
NCT01245348 completednot on this mapstarted 2010, after this paper: background citation

Relative Effectiveness of Schizophrenia Therapy (REST) Study

TypeobservationalSponsorMedco Health Solutions, Inc.Ran2010 to 2012Enrolled1,110ConditionsSchizophrenia, Bipolar DisorderArmsSULT4A1-1 genetic test
NCT01623713 phase2completednot on this mapstarted 2012, after this paper: background citation

A Randomized, Double-Blind, Active-Controlled, Multicenter Study to Evaluate Efficacy and Safety Study of Iloperidone Virus Risperidone to Treat Schizophrenia

TypeinterventionalSponsorJiangsu Hansoh Pharmaceutical Co., Ltd.Ran2012 to 2013Enrolled260ConditionsSchizophrenia, Iloperidone, EfficacyArmsiloperidone, Risperidone
NCT01844700 phase4terminatednot on this mapstarted 2013, after this paper: background citation

1/2-MC4R Genotype and Pediatric Antipsychotic Drug- Induced Weight Gain

TypeinterventionalSponsorNorthwell HealthRan2013 to 2014Enrolled14ConditionsHigh Risk MC4R Genotype, Low Risk MC4R Genotype, One Week or Less Antipsychotic Lifetime ExposureArmsZiprasidone, aripiprazole, quetiapine, or risperidone
NCT02451670 nacompletednot on this mapstarted 2016, after this paper: background citation

Reducing Cardiovascular Risk in Adults With Serious Mental Illness Using an Electronic Medical Record-based Clinical Decision Support

TypeinterventionalSponsorHealthPartners InstituteRan2016 to 2018Enrolled10,347ConditionsChronic Disease, Mental Disorder, Health Behavior, Bipolar DisorderArmsPrioritized Clinical Decision Support
NCT02624167 phase2completednot on this mapstarted 2015, after this paper: background citation

A Phase IIA, Prospective, Randomized, Double-blind, Multiple-dose Study of NW-3509A in Chronic Schizoprhenia Patients Not Responding to Their Current Anti-psychotic Medication

TypeinterventionalSponsorNewron Pharmaceuticals SPARan2015 to 2017Enrolled90ConditionsChronic SchizophreniaArmsNW-3509A, Placebo
NCT02634684 phase2completednot on this mapstarted 2014, after this paper: background citation

Pharmacologic Augmentation of Neurocognition and Cognitive Training in Psychosis

TypeinterventionalSponsorUniversity of California, San DiegoRan2014 to 2020Enrolled82ConditionsSchizophreniaArmsDextroamphetamine, Placebo
NCT03907124 phase4withdrawnnot on this mapstarted 2019, after this paper: background citation

Clinical Utility of Pharmacogenomics of Psychotropic Medications

TypeinterventionalSponsorOregon Health and Science UniversityRan2019 to 2021Enrolled0ConditionsPsychiatric Disorders, PainArmsGenetically-guided treatment with FDA-approved psychotropic drugs, Treatment as usual (TAU)
NCT05001399 nacompletednot on this mapstarted 2021, after this paper: background citation

Feasibility of Using Holographic Memory Resolution® (HMR) in Patients/Clients With Pain

TypeinterventionalSponsorBillings ClinicRan2021 to 2022Enrolled60ConditionsChronic Pain, Headache, Migraine, Stress Disorders, Post-TraumaticArmsHolographic Memory Resolution® (HMR)
NCT06700967 not yet recruitingnot on this mapstarted 2024, after this paper: background citation

A Precision Medication Guidance Model for Schizophrenia Based on Pharmacogenomics and Physiologically Based Pharmacokinetics: a Real-World Observational Study

TypeobservationalSponsorShanghai Mental Health CenterRan2024 to 2025Enrolled400ConditionsSchizophenia Disorder
3 · Its place in the literature

Who cites it

1,716 citing papers in PubMed, 11 syntheses or guidelines pooled it, 5,867 citations in OpenAlex.

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1,656 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Jeffrey A LiebermanDepartment of Psychiatry, College of Physicians and Surgeons, Columbia University, New York State Psychiatric Institute, New York, NY 10032, USA. jlieberman@columbia.edu
T Scott Stroup
Joseph P McEvoy
Marvin S Swartz
Robert A Rosenheck
Diana O Perkins
Richard S E Keefe
Sonia M Davis
Clarence E Davis
Barry D Lebowitz
Joanne Severe
John K Hsiao
Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) Investigators
New York College of Health Professions · USColumbia University · US

Funding

PUBLIC EDUCATION CAMPAIGN ON DEPRESSION DARTN01MH090001 · NIMH · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · 1989 to 2003
$10.4M
STN/Three Individual Projects: COATS, METS, CRSTNN01MH90001 · NIMH · UNIV OF NORTH CAROLINA CHAPEL HILL · PI STROUP, SCOTT · 2007 to 2009
$6.7M
NIMH NIH HHS N01 MH90001
6 · The paper itself

Abstract

backgroundThe relative effectiveness of second-generation (atypical) antipsychotic drugs as compared with that of older agents has been incompletely addressed, though newer agents are currently used far more commonly. We compared a first-generation antipsychotic, perphenazine, with several newer drugs in a double-blind study.

methodsA total of 1493 patients with schizophrenia were recruited at 57 U.S. sites and randomly assigned to receive olanzapine (7.5 to 30 mg per day), perphenazine (8 to 32 mg per day), quetiapine (200 to 800 mg per day), or risperidone (1.5 to 6.0 mg per day) for up to 18 months. Ziprasidone (40 to 160 mg per day) was included after its approval by the Food and Drug Administration. The primary aim was to delineate differences in the overall effectiveness of these five treatments.

resultsOverall, 74 percent of patients discontinued the study medication before 18 months (1061 of the 1432 patients who received at least one dose): 64 percent of those assigned to olanzapine, 75 percent of those assigned to perphenazine, 82 percent of those assigned to quetiapine, 74 percent of those assigned to risperidone, and 79 percent of those assigned to ziprasidone. The time to the discontinuation of treatment for any cause was significantly longer in the olanzapine group than in the quetiapine (P<0.001) or risperidone (P=0.002) group, but not in the perphenazine (P=0.021) or ziprasidone (P=0.028) group. The times to discontinuation because of intolerable side effects were similar among the groups, but the rates differed (P=0.04); olanzapine was associated with more discontinuation for weight gain or metabolic effects, and perphenazine was associated with more discontinuation for extrapyramidal effects.

conclusionsThe majority of patients in each group discontinued their assigned treatment owing to inefficacy or intolerable side effects or for other reasons. Olanzapine was the most effective in terms of the rates of discontinuation, and the efficacy of the conventional antipsychotic agent perphenazine appeared similar to that of quetiapine, risperidone, and ziprasidone. Olanzapine was associated with greater weight gain and increases in measures of glucose and lipid metabolism.

Indexed as

AdultAntipsychotic AgentsBenzodiazepinesChronic DiseaseDibenzothiazepinesDouble-Blind MethodFemaleHumansLipidsMaleOlanzapinePatient CompliancePerphenazinePiperazinesProportional Hazards ModelsQuetiapine FumarateAntipsychotic AgentsBenzodiazepinesDibenzothiazepinesLipidsOlanzapinePerphenazinePiperazinesQuetiapine FumarateRisperidoneThiazolesziprasidone

Identifiers

PMID16172203
OpenAlexW2159155203

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

and 4 more above

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.