Switching From Oral Antipsychotics to Long-Acting Risperidone in Participants With Schizophrenia
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Purpose
The purpose of this study is to evaluate efficacy, safety and tolerance of long-acting risperidone when switching from oral antipsychotics in participants with schizophrenia (psychiatric disorder with symptoms of emotional instability, detachment from reality, often with delusions and hallucinations, and withdrawal into the self).
| Condition | Intervention | Phase |
|---|---|---|
|
Schizophrenia |
Drug: Risperidone prolonged release |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Endpoint Classification: Safety/Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | An Open-Label Study of Oral Antipsychotics Replacement by Prolonged Release Risperidone (Risperdal Consta) in Schizophrenic Subjects With Bad Adhesion to the Treatment |
- Positive and Negative Syndromes Scale (PANSS) total score at Baseline [ Time Frame: Baseline ] [ Designated as safety issue: No ]The PANSS is a 30-item scale designed to assess various symptoms of schizophrenia including delusions, grandiosity, blunted affect, poor attention, and poor impulse control. The 30 symptoms are rated on a 7-point scale that ranges from 1 (absent) to 7 (extreme psychopathology). The PANSS total score consists of the sum of all 30 PANSS items and ranges from 30 to 210. Higher scores indicate worsening.
- Positive and Negative Syndromes Scale (PANSS) total score at Week 2 [ Time Frame: Week 2 ] [ Designated as safety issue: No ]The PANSS is a 30-item scale designed to assess various symptoms of schizophrenia including delusions, grandiosity, blunted affect, poor attention, and poor impulse control. The 30 symptoms are rated on a 7-point scale that ranges from 1 (absent) to 7 (extreme psychopathology). The PANSS total score consists of the sum of all 30 PANSS items and ranges from 30 to 210. Higher scores indicate worsening.
- Positive and Negative Syndromes Scale (PANSS) total score at Week 4 [ Time Frame: Week 4 ] [ Designated as safety issue: No ]The PANSS is a 30-item scale designed to assess various symptoms of schizophrenia including delusions, grandiosity, blunted affect, poor attention, and poor impulse control. The 30 symptoms are rated on a 7-point scale that ranges from 1 (absent) to 7 (extreme psychopathology). The PANSS total score consists of the sum of all 30 PANSS items and ranges from 30 to 210. Higher scores indicate worsening.
- Positive and Negative Syndromes Scale (PANSS) total score at Week 8 [ Time Frame: Week 8 ] [ Designated as safety issue: No ]The PANSS is a 30-item scale designed to assess various symptoms of schizophrenia including delusions, grandiosity, blunted affect, poor attention, and poor impulse control. The 30 symptoms are rated on a 7-point scale that ranges from 1 (absent) to 7 (extreme psychopathology). The PANSS total score consists of the sum of all 30 PANSS items and ranges from 30 to 210. Higher scores indicate worsening.
- Positive and Negative Syndromes Scale (PANSS) total score at Week 16 [ Time Frame: Week 16 ] [ Designated as safety issue: No ]The PANSS is a 30-item scale designed to assess various symptoms of schizophrenia including delusions, grandiosity, blunted affect, poor attention, and poor impulse control. The 30 symptoms are rated on a 7-point scale that ranges from 1 (absent) to 7 (extreme psychopathology). The PANSS total score consists of the sum of all 30 PANSS items and ranges from 30 to 210. Higher scores indicate worsening.
- Positive and Negative Syndromes Scale (PANSS) total score at Week 24 [ Time Frame: Week 24 ] [ Designated as safety issue: No ]The PANSS is a 30-item scale designed to assess various symptoms of schizophrenia including delusions, grandiosity, blunted affect, poor attention, and poor impulse control. The 30 symptoms are rated on a 7-point scale that ranges from 1 (absent) to 7 (extreme psychopathology). The PANSS total score consists of the sum of all 30 PANSS items and ranges from 30 to 210. Higher scores indicate worsening.
- Clinical Global Impressions (CGI) - Disease Severity score [ Time Frame: Baseline up to Week 24 ] [ Designated as safety issue: No ]The CGI rating scale is a 7 point global assessment that measures the clinician's impression of the severity of illness exhibited by a participant. A rating of 1 is equivalent to "Normal, not at all ill" and a rating of 7 is equivalent to "Among the most extremely ill participants". Higher scores indicate worsening.
- Extrapyramidal Symptoms Rating Scale (ESRS) total score [ Time Frame: Baseline up to Week 24 ] [ Designated as safety issue: Yes ]The ESRS is used to assess four types of drug-induced movement disorders administered as a questionnaire. Score range from 0 to 6 (0 is absent and 6 is extremely severe).
- Drug Attitude Inventory (DAI-10) [ Time Frame: Screening up to Week 24 ] [ Designated as safety issue: Yes ]The DAI-10 is a 10-item questionnaire to assess 1) subjective experience of drug and 2) attitudes and beliefs toward neuroleptics which may influence compliance in schizophrenia participants. It is the binary scale assessing the participant's subjective response. A 'compliant' response is scored as +1; a dysphoric response is scored as -1. A positive sum of items indicates a positive subjective response (SR); a negative sum of scores indicates a negative SR (non-compliant).
- Short Form-36 (SF-36) - Quality of life [ Time Frame: Screening up to Week 24 ] [ Designated as safety issue: No ]The SF-36 is a survey of participant health. It consists of eight scaled scores, which are the weighted sums of the questions in their section. The eight sections are: vitality, physical functioning, bodily pain, general health perceptions, physical role functioning, emotional role functioning, social role functioning, and mental health. Each item is scored on a 0-100 range so that the lowest and highest possible scores are set at 0 and 100, respectively. All items are scored so that a high score defines a more favorable health state.
| Enrollment: | 53 |
| Study Start Date: | January 2006 |
| Study Completion Date: | March 2008 |
| Primary Completion Date: | March 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: Risperidone prolonged release |
Drug: Risperidone prolonged release
Risperidone will be administered as intramuscular injection as 25 milligram (mg) every two weeks, from Week 1 to 24, wherein after Week 3, dose may be adjusted up to 50 mg at physician criterion. For first two weeks, previous oral antipsychotic drug will be maintained and the dose will be gradually decreased and will cease at Week 3.
Other Name: - Risperdal consta
|
Detailed Description:
This is an open-label (all people know the identity of the intervention), multi-centric (conducted in more than one center) and non-comparative study of risperidone in participants with schizophrenia who have a previous history (in the last 12 months) of bad adherence to the antipsychotic treatment of first or second oral generation. The duration of this study will be 24 weeks and will include following visits: Screening, Baseline, Week 2, 4, 8, 12, 16, 20 and 24 (End visit or early withdrawal). All the eligible participants (after risperidone intolerance test during screening) will receive a dose of 25 milligram risperidone every two weeks by intramuscular injection (injection of a substance into a muscle). Efficacy and safety of the participants will primarily be evaluated by Positive and Negative Syndromes Scale and Extrapyramidal Symptom Rating Scale, respectively. Participants' safety will be monitored throughout the study.
Eligibility| Ages Eligible for Study: | 18 Years to 50 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Have schizophrenia diagnosis by Diagnostic and Statistical Manual of Mental Disorders, fourth edition (DSM-IV)
- Be on treatment with oral antipsychotic of first or second generation, for a minimum time of 12 months
- Previous history of bad adhesion to oral antipsychotic treatment in the last 12 months
- Total Positive and Negative Syndrome Scale score less than or equal to 90, the conceptual disorganization, hallucinatory behavior, suspicion and not usual content of thought must be less than or equal to 4
- Be not pregnant as showed on negative pregnancy serum test
Exclusion Criteria:
- Contraindication or known hypersensitivity to risperidone
- Previous history of unsatisfactory response to risperidone
- Previous history of refractivity to the other second generation antipsychotics
- Use of antipsychotic of intramuscular deposit in the last 12 months
- Other mental disturbances of DSM-IV axis
Contacts and Locations| Brazil | |
| Curitiba, Brazil | |
| Porto Alegre, Brazil | |
| Rio De Janeiro, Brazil | |
| Salvador, Brazil | |
| Sao Paulo, Brazil | |
| Study Director: | Janssen-Cilag Ltd. Clinical trial | Janssen-Cilag Ltd. |
More Information
No publications provided
| Responsible Party: | Janssen-Cilag Ltd. |
| ClinicalTrials.gov Identifier: | NCT01726335 History of Changes |
| Other Study ID Numbers: | CR012484, RISSCH4135 |
| Study First Received: | November 9, 2012 |
| Last Updated: | March 8, 2013 |
| Health Authority: | Brazil: Ethics Committee |
Keywords provided by Janssen-Cilag Ltd.:
|
Schizophrenia Risperidone Risperdal consta |
Additional relevant MeSH terms:
|
Schizophrenia Schizophrenia and Disorders with Psychotic Features Mental Disorders Antipsychotic Agents Risperidone Tranquilizing Agents Central Nervous System Depressants Physiological Effects of Drugs Pharmacologic Actions |
Central Nervous System Agents Therapeutic Uses Psychotropic Drugs Serotonin Antagonists Serotonin Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Dopamine Antagonists Dopamine Agents |
ClinicalTrials.gov processed this record on May 19, 2013