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Long-acting Paliperidone Palmitate Injection and Olanzapine for Schizophrenia

Primary Purpose

Schizophrenia

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Olanzapine
Paliperidone
Sponsored by
Beijing HuiLongGuan Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Schizophrenia focused on measuring schizophrenia, clinical trial, olanzapine, paliperidone

Eligibility Criteria

18 Years - 45 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Diagnosis of schizophrenia or schizophreniform disorder;
  • Duration of symptoms not longer than 60 months;
  • No prior treatment with antipsychotic medication or, if previously treated, a total lifetime usage of less than 14 days;
  • Between 18 and 45 years of age; and
  • Current psychotic symptoms of moderate severity.

Exclusion Criteria:

  • A DSM-IV Axis I diagnosis other than schizophrenia or schizophreniform;
  • Documented disease of the central nervous system that can interfere with the trial assessments including, but not limited to stroke, tumor, Parkinson's disease, Huntington's disease, seizure disorder, history of brain trauma resulting in significant impairment, chronic, infection;
  • Acute, unstable and/or significant and untreated medical illness (e.g., infection, unstable diabetes, uncontrolled hypertension);
  • A clinically significant ECG abnormality in the opinion of the investigator;
  • Pregnant or breast-feeding female;
  • Use of disallowed concomitant therapy;
  • History of severe allergy or hypersensitivity.

Sites / Locations

  • Beijing HuiLongGuan Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Paliperidone

Olanzapine

Arm Description

Drug: Paliperidone, 75-150mg/month, once a month, 12 weeks

Drug: Olanzapine, 20mg/day, twice a day, 12 weeks

Outcomes

Primary Outcome Measures

Symptoms assessed on PANSS.
Clinical symptoms

Secondary Outcome Measures

Clinical global impression assessed on CGI.
clinical severity
Cognitive functioning assessed on RBANS.
cognitive performance
Number of weight change in treatment assessed on Weight gain.
weight gain
Abnormal Involuntary Movement Scale assessed Abnormal Involuntary Movement Scale assessed on AIMS.
Side effects

Full Information

First Posted
September 20, 2016
Last Updated
January 16, 2018
Sponsor
Beijing HuiLongGuan Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02918825
Brief Title
Long-acting Paliperidone Palmitate Injection and Olanzapine for Schizophrenia
Official Title
A Randomized Trial to Compare the Efficiency and Side Effect Between Olanzapine and Long-acting Paliperidone Palmitate Injection in Schizophrenia
Study Type
Interventional

2. Study Status

Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
September 1, 2016 (Actual)
Primary Completion Date
August 30, 2017 (Actual)
Study Completion Date
September 30, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Beijing HuiLongGuan Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
A randomized trial of olanzapine and Long-acting paliperidone palmitate injection in the treatment of 100 treatment- naive first-episode patients with schizophrenia.
Detailed Description
OBJECTIVE: Investigator compared the efficiency, social function, cognitive function and side effect of olanzapine and Long-acting paliperidone palmitate injection in the treatment of first-episode drug-naive patients with schizophrenia. METHODS: Clinical Trial: This is a randomized trial in treatment-naive first-episode patients with schizophrenia. The study consists of a 1-week stabilization phase, followed by 12 weeks of treatment. The total trial duration is 13 weeks. Assessment Procedures: 2.1. Primary Outcome Variable-psychopathology: Assessment instruments include the Positive and Negative Syndrome Scale (PANSS), the Assessment of Negative Symptoms (SANS) and the Clinical Global Impression (ICG). Patients are interviewed at screening, at week-4, at week-1, at baseline and at every two weeks, for a total of 12 ratings. 2.2. Cognitive tests: A comprehensive battery of tests encompassing the cognitive domains of executive function, attention, memory, perception, and general intellect is administered twice at baseline and at the end of 16-week treatment by a trained psychologist. Scoring follows standardized procedures. The Wisconsin Card Sorting Test (WCST) is administered as a measure of executive function. The N-back (0-3 back) test is administered as a measure of working memory. Logical Memory I and II, Verbal Paired Associates I and II, Visual Reproduction I and II and Digits Forward from the Wechsler Memory Scale-Revised (WMS-R) are administered as a tests of episodic memory. The Distractibility version of Gordon Continuous Performance Test (CPT)is administered as a test of attention. A four-subtest version of the Wechsler Adult Intelligence Scale-Revised (WAIS-R), consisting of the Arithmetic, Similarities, Picture Completion, and Digit Symbol Substitution tests is administered to obtain an estimate of current Full- Scale Intelligence Quotient (FSIQ). 2.3. Social functioning: The Personal and Social Performance Scale (PSP) examines the four dimensions of social functioning: Socially useful activities including work and study, personal and social relationships, self-care, disturbing and aggressive behaviors. 2.4. Side Effects: Parkinsonism is rated with the Simpson-Angus Scale for extrapyramidal side effects (SAS). The Abnormal Involuntary Movement Scale (AIMS) is chosen to assess tardive dyskinesia (TD) severity. All of the AIMS and Simpson-Angus Rating Scales are administered by the same investigator, at screening, at week-4, at week-1, at baseline and at baseline and at every two weeks, for a total of 12 ratings. 2.5.Weight gain measurement: weight gain every week 2.6. Serum measurement: triglyceride, blood sugar,cholesterol,blood pressure

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenia
Keywords
schizophrenia, clinical trial, olanzapine, paliperidone

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Paliperidone
Arm Type
Experimental
Arm Description
Drug: Paliperidone, 75-150mg/month, once a month, 12 weeks
Arm Title
Olanzapine
Arm Type
Active Comparator
Arm Description
Drug: Olanzapine, 20mg/day, twice a day, 12 weeks
Intervention Type
Drug
Intervention Name(s)
Olanzapine
Intervention Description
Olanzapine
Intervention Type
Drug
Intervention Name(s)
Paliperidone
Intervention Description
Paliperidone
Primary Outcome Measure Information:
Title
Symptoms assessed on PANSS.
Description
Clinical symptoms
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Clinical global impression assessed on CGI.
Description
clinical severity
Time Frame
12 weeks
Title
Cognitive functioning assessed on RBANS.
Description
cognitive performance
Time Frame
12 weeks
Title
Number of weight change in treatment assessed on Weight gain.
Description
weight gain
Time Frame
12 weeks
Title
Abnormal Involuntary Movement Scale assessed Abnormal Involuntary Movement Scale assessed on AIMS.
Description
Side effects
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Diagnosis of schizophrenia or schizophreniform disorder; Duration of symptoms not longer than 60 months; No prior treatment with antipsychotic medication or, if previously treated, a total lifetime usage of less than 14 days; Between 18 and 45 years of age; and Current psychotic symptoms of moderate severity. Exclusion Criteria: A DSM-IV Axis I diagnosis other than schizophrenia or schizophreniform; Documented disease of the central nervous system that can interfere with the trial assessments including, but not limited to stroke, tumor, Parkinson's disease, Huntington's disease, seizure disorder, history of brain trauma resulting in significant impairment, chronic, infection; Acute, unstable and/or significant and untreated medical illness (e.g., infection, unstable diabetes, uncontrolled hypertension); A clinically significant ECG abnormality in the opinion of the investigator; Pregnant or breast-feeding female; Use of disallowed concomitant therapy; History of severe allergy or hypersensitivity.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiang Zhang, MD, PhD
Organizational Affiliation
The University of Texas Health Science Center, Houston
Official's Role
Principal Investigator
Facility Information:
Facility Name
Beijing HuiLongGuan Hospital
City
Beijing
ZIP/Postal Code
100096
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Data will be available on request
Citations:
PubMed Identifier
27629292
Citation
Kim E, Correll CU, Mao L, Starr HL, Alphs L. Once-monthly paliperidone palmitate compared with conventional and atypical daily oral antipsychotic treatment in patients with schizophrenia. CNS Spectr. 2016 Dec;21(6):466-477. doi: 10.1017/S1092852916000444. Epub 2016 Sep 15.
Results Reference
result
PubMed Identifier
27627971
Citation
Yoshimura R, Hori H, Katsuki A, Atake K. Marked Improvement of Meige Syndrome in a Japanese Male Patient with Schizophrenia After Switching from Risperidone to Paliperidone: A Case Report. J UOEH. 2016 Sep;38(3):233-6. doi: 10.7888/juoeh.38.233.
Results Reference
result
PubMed Identifier
27574835
Citation
Young-Xu Y, Duh MS, Muser E, DerSarkissian M, Faust E, Kageleiry A, Bhak RH, Fu DJ, Lefebvre P, Shiner B. Impact of Paliperidone Palmitate Versus Oral Atypical Antipsychotics on Health Care Resource Use and Costs in Veterans with Schizophrenia. J Clin Psychiatry. 2016 Oct;77(10):e1332-e1341. doi: 10.4088/JCP.16m10745.
Results Reference
result

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Long-acting Paliperidone Palmitate Injection and Olanzapine for Schizophrenia

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