Differences in Schizophrenia With One-month and 3-month Paliperidone Palmitate Treatment
Primary Purpose
Schizophrenics
Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Paliperidone Palmitate 156 MG/ML Prefilled Syringe [Invega]
Paliperidone Palmitate 546 MG Intramuscular Suspension, Extended Release [INVEGA TRINZA]
Sponsored by

About this trial
This is an interventional treatment trial for Schizophrenics focused on measuring paliperidone palmitate, social function, cognitive function, quality of life
Eligibility Criteria
Inclusion Criteria:
- All of them had to meet the diagnostic criteria for schizophrenia according to the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV).
Exclusion Criteria:
- Patients who had comorbid serious medical illnesses, and may therefore present substantial clinical risk due to pharmacotherapy, were excluded from the sample, as were pregnant and lactating women.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
INVEGA Sustenna
INVEGA Trinza
Arm Description
INVEGA Sustenna is a one month long-acting injection (PP1M)
INVEGA Trinza is a three month long-acting injection (PP3M)
Outcomes
Primary Outcome Measures
Personal and Social Performance scales (PSP)
Personal and Social Performance scales was assessed for the evaluation of psychosocial functioning. A higher score represents better psychosocial functioning.
Short-version of the Udvalg for Kliniske Undersogelser (short-version UKU)
The Short-version of the Udvalg for Kliniske Undersogelser was assessed for the evaluation of psychic side effect. A higher score present to a mild or severe degree symptoms.
Wisconsin Card Sorting test (WCST)
Wisconsin Card Sorting Test was assessed for the performance of cognitive function. A higher score in conceptual level response and lower score in percent of perseverative errors present to greater cognitive function.
Secondary Outcome Measures
Full Information
NCT ID
NCT04754750
First Posted
January 27, 2021
Last Updated
February 12, 2021
Sponsor
Calo Psychiatric Center
1. Study Identification
Unique Protocol Identification Number
NCT04754750
Brief Title
Differences in Schizophrenia With One-month and 3-month Paliperidone Palmitate Treatment
Official Title
Differences in Lipid and Cognitive Change Between One-month and 3-month Paliperidone Palmitate Treatment in Stable Schizophrenia
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
January 2015 (Actual)
Primary Completion Date
June 2017 (Actual)
Study Completion Date
June 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Calo Psychiatric Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Schizophrenia is a chronic and severe psychiatric disorder, these patients suffer from positive symptoms, negative symptoms and cognitive deficits, of which working memory problems are considered a central cognitive impairment. Atypical antipsychotics are believed to have a superior effect in reducing both positive and negative symptoms of schizophrenia, coupled with a low risk of extrapyramidal symptoms. Particularly, 2nd-generation antipsychotic medications are commonly used in treatment of schizophrenia. An antipsychotic drug, Paliperidone palmitate (PDP), is administered to patients with schizophrenia as injections at one-month (PP1M) or three-month (PP3M) intervals. This study was compare the effects of treatment, social function, and side effects between PP1M and PP3M in patients with schizophrenia. Moreover, the changes of cognitive and lipid profile between two PDP were also explored. Firstly, participants were received the one month long-acting injection (PP1M) three months. Then, the stable participants were shifted to the three month long-acting injection (PP3M). Concomitant medications were allowed to prescribe except other antipsychotics. Outcome measurements were 20-item Toronto Alexithymia Scale (TAS-20), 45-itme quality of life for mental disorder (QOLMD), Short-version of the Udvalg for Kliniske Undersogelser (short-version UKU), and Wisconsin Card Sorting test (WCST). These measurements were performed every three-month except WCST which was performed every six-month. The different effects of PP1M and PP3M will be expected to find out in this study.
Detailed Description
This is a two and half-one years, single-arm, nonrandomized, open-label study which was conducted between Jan 2015 to Jun 2017 including from a psychiatric center in southern Taiwan. The stable schizophrenic patients who previously received risperidone long-acting injection for more than one year and shifted to paliperidone palmitate after including in the study. Firstly, participants were received the one month long-acting injection (PP1M) three months. Then, the stable participants were shifted to the three month long-acting injection (PP3M). Concomitant medications were allowed to prescribe except other antipsychotics. Outcome measurements were 20-item Toronto Alexithymia Scale (TAS-20), 45-itme quality of life for mental disorder (QOLMD), Short-version of the Udvalg for Kliniske Undersogelser (short-version UKU), and Wisconsin Card Sorting test (WCST). These measurements were performed every three-month except WCST which was performed every six-month. The effect of treatment was assessed using Personal and Social Performance (PSP) scales for the evaluation of psychosocial functioning at 0, 4, 8, and 12 weeks in first study, and at 0, 3, 6, 9, 12 months in second study, respectively. In addition, all participants were assessed for body weight, waist circumference, and blood lipid profile. To evaluate the lipid profiles, fasting blood samples were analyzed for total cholesterol (TC), Triglyceride (TG), High-density Lipoprotein (HDL) and Low-density Lipoprotein (LDL). These blood samples were collected at every month until study completion.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Schizophrenics
Keywords
paliperidone palmitate, social function, cognitive function, quality of life
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Sequential Assignment
Model Description
Total of 72 participants, including 41 men and 31 female, were received the PP1M three months. The stable participants were shifted to PP3M for one year.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
72 (Actual)
8. Arms, Groups, and Interventions
Arm Title
INVEGA Sustenna
Arm Type
Active Comparator
Arm Description
INVEGA Sustenna is a one month long-acting injection (PP1M)
Arm Title
INVEGA Trinza
Arm Type
Active Comparator
Arm Description
INVEGA Trinza is a three month long-acting injection (PP3M)
Intervention Type
Drug
Intervention Name(s)
Paliperidone Palmitate 156 MG/ML Prefilled Syringe [Invega]
Other Intervention Name(s)
Sustenna
Intervention Type
Drug
Intervention Name(s)
Paliperidone Palmitate 546 MG Intramuscular Suspension, Extended Release [INVEGA TRINZA]
Other Intervention Name(s)
Trinza
Primary Outcome Measure Information:
Title
Personal and Social Performance scales (PSP)
Description
Personal and Social Performance scales was assessed for the evaluation of psychosocial functioning. A higher score represents better psychosocial functioning.
Time Frame
15 months
Title
Short-version of the Udvalg for Kliniske Undersogelser (short-version UKU)
Description
The Short-version of the Udvalg for Kliniske Undersogelser was assessed for the evaluation of psychic side effect. A higher score present to a mild or severe degree symptoms.
Time Frame
15 months
Title
Wisconsin Card Sorting test (WCST)
Description
Wisconsin Card Sorting Test was assessed for the performance of cognitive function. A higher score in conceptual level response and lower score in percent of perseverative errors present to greater cognitive function.
Time Frame
15 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
69 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All of them had to meet the diagnostic criteria for schizophrenia according to the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV).
Exclusion Criteria:
Patients who had comorbid serious medical illnesses, and may therefore present substantial clinical risk due to pharmacotherapy, were excluded from the sample, as were pregnant and lactating women.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
For-Wey Lung, MD, ScD
Organizational Affiliation
Calo Psychiatric Center
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Differences in Schizophrenia With One-month and 3-month Paliperidone Palmitate Treatment
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