Correlation Between Cognitive Function and Relapse of Schizophrenia Regarding Dose Reduction
NCT ID: NCT03019887
Last Updated: 2021-09-09
Study Results
Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.
View full resultsBasic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
139 participants
INTERVENTIONAL
2011-04-30
2017-01-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effective Adjunctive Use of Pergolide for Cognitive Impairment and Negative Symptoms in Schizophrenia
NCT00197483
Self-Management Therapy for Youth With Schizophrenia
NCT00000387
Study on Abnormal Dopamine Synthesis and Connectivity According to the Antipsychotic Treatment Response in Schizophrenia
NCT02248987
Effects of Eszopiclone on Sleep-dependent Learning in Schizophrenia
NCT00833547
Cognition, Functioning and Quality of Life
NCT00182442
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
reduction group
dose reduction of antipsychotics at a rate not exceeding 50mg chlorpromazine equivalent/week
reduction of risperidone, haloperidol, olanzapine, quetiapine, aripiprazole, paliperidone, levomepromazine, perphenazine
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
reduction of risperidone, haloperidol, olanzapine, quetiapine, aripiprazole, paliperidone, levomepromazine, perphenazine
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* those in the chronic phase receiving mean daily antipsychotic doses exceeding 1000-mg chlorpromazine eq./day.
Exclusion Criteria
* substance abuse or dependence,
* a history of major head trauma,
* serious medical or neurological disorders, or
* depot antipsychotic injections within the previous 3 months and electroconvulsive therapy within the previous 6 months
20 Years
70 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Juntendo University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Ryota Ataniya
Clinician, graduate student
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Takahashi Tadashi
Role: STUDY_CHAIR
Okada hospital
Mikiro Saito
Role: STUDY_CHAIR
Okada hospital
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
673
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.