An Efficacy and Safety Study of Long-Term Risperidone Microspheres in Participants With Schizophrenia
2014年3月25日 更新者：Janssen Korea, Ltd., Korea
Effect on Efficacy, Safety and Quality of Life by Long-Term Treatment of Long-Acting Risperidone Microspheres in Patients With Schizophrenia
The purpose of this study is to evaluate the long-term efficacy and safety of a long-acting injectable formulation of risperidone (an antipsychotic medication) and its influence on quality of life, in participants with schizophrenia (psychiatric disorder with symptoms of emotional instability, detachment from reality, often with delusions and hallucinations, and withdrawal into the self).
調査の概要
詳細な説明
This is an open-label (all people know the identity of the intervention) single-arm, and prospective study (study following participants forward in time) of risperidone microspheres in participants with schizophrenia.
Participants will be treated with intramuscular (into a muscle) injections of either 25 milligram (mg) or 37.5 mg or 50 mg of risperidone twice weekly, every 2 weeks for 2 years.
The total duration of study will be 2 years.
The efficacy of participants will primarily be evaluated by total Positive and Negative Syndrome Scale (PANSS) score.
Participants' quality of life and safety will be monitored throughout the study.
研究の種類
介入
入学 (実際)
40
段階
- フェーズ 4
連絡先と場所
このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。
研究場所
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Seoul、大韓民国
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参加基準
研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。
適格基準
就学可能な年齢
18年～65年 (大人、高齢者)
健康ボランティアの受け入れ
いいえ
受講資格のある性別
全て
説明
Inclusion Criteria:
- Participants diagnosed with schizophrenia or schizoaffective disorder (in-patients or out-patients)
- Participants currently having their symptoms well controlled with a stable dose of oral antipsychotic medication
- Participants who have signed informed consent form Exclusion Criteria:
- Participants who have never received any previous antipsychotic treatment
- Participants who have received clozapine during the last 3 months
- Participants with a serious unstable medical condition, including laboratory abnormalities
- Participants with a history of, or current symptoms of tardive dyskinesia (a complication of neuroleptic therapy involving involuntary movements of facial muscles) or neuroleptic malignant syndrome (a rare psychotropic-drug reaction, which may be characterized by confusion, reduced consciousness, high fever or pronounced muscle stiffness)
- Female participants who are pregnant or breast-feeding, or are of childbearing age without adequate contraception
研究計画
このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。
研究はどのように設計されていますか？
デザインの詳細
- 主な目的：処理
- 割り当て：なし
- 介入モデル：単一グループの割り当て
- マスキング：なし（オープンラベル）
武器と介入
参加者グループ / アーム |
介入・治療 |
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実験的：Risperidone Long-Acting Injectable (RLAI)
The RLAI 25 milligram (mg) or 37.5 mg or 50 mg will be administered intramuscularly (into a muscle) depending on Investigator's discretion every 2 weeks for 2 years.
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The RLAI 25 mg or 37.5 mg or 50 mg will be administered intramuscularly depending on Investigator's discretion every 2 weeks for 2 years.
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この研究は何を測定していますか？
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Change From Baseline in Total Positive and Negative Syndrome Scale (PANSS) Score at Week 96
時間枠：Baseline and Week 96
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The PANSS is a 30-item scale consisting of 3 subscales, the positive subscale (7 items), the negative subscale (7 items), and the general psychopathology subscale (16 items) and it is designed to assess various symptoms of schizophrenia including delusions, grandiosity, blunted affect, poor attention, and poor impulse control.
The 30 items are rated on a 7-point scale that ranges from 1 (absent) to 7 (extreme).
The PANSS total score consists of the sum of all 30 PANSS items and ranges from 30 (absent) to 210 (extreme ill).
Higher scores indicate worsening.
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Baseline and Week 96
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Change From Baseline in Clinical Global Impression-Severity (CGI-S) Score at Week 96
時間枠：Baseline and Week 96
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The CGI-S rating scale is used to rate the severity of a participant's psychotic condition on a 7-point scale.
It is rated as follows: 1=Normal, not at all ill, 2=Borderline mentally ill, 3=Mildly ill, 4=Moderately ill, 5=Markedly ill, 6=Severely ill, and 7=Among the most extremely ill.
Higher scores indicate worsening.
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Baseline and Week 96
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Change From Baseline in Global Assessment of Functioning (GAF) Score at Week 96
時間枠：Baseline and Week 96
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GAF is a 100-point tool rating overall psychological, social and occupational functioning of adults.
The higher score range (91-100) refers to a superior functioning in a wide range of activities, and absence of symptoms.
The lower score range (1-10) refers to persistent danger of severely hurting self or others; or persistent inability to maintain minimum personal hygiene; or serious suicidal act with clear expectation of death.
Lower scores indicate worsening.
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Baseline and Week 96
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Change From Baseline in World Health Organization (WHO)-Quality of Life (QOL) at Week 96
時間枠：Baseline and Week 96
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The WHOQOL-BREF is a 26-item, self-report questionnaire and short version of WHOQOL-100, consisting of 4 domains: physical health (7 items), psychological health (6 items), social relationships (3 items), and environmental health (8 items); it also contains QOL and general health items.
Domain scores are scaled in a positive direction (i.e. higher scores denote higher quality of life).
The mean score of items within each domain is used to calculate the domain score.
Each individual item of the WHOQOL-BREF is scored from 1=not at all to 5=completely on a response scale, which is stipulated as a 5-point ordinal scale.
The scores are then transformed linearly to a scale of 0 (the worse quality of life) to 100 (the worse quality of life).
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Baseline and Week 96
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Change From Baseline in Neurocognitive Function Test (NCFT): General Intelligence (Korean-Wechsler Adults Intelligence Scale [K-WAIS]) at Week 96
時間枠：Baseline and Week 96
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The K-WAIS is a Korean version of the Wechsler Adult Intelligence Scale-Revised (WAIS-R).
It is an intelligence test that assess 3 general areas of intelligence quotients (IQ): verbal IQ, performance IQ and full-scale IQ (FSIQ).
The verbal IQ includes: Digit Span, Vocabulary, and Arithmetic; performance IQ includes: Picture Arrangement and Block Design; and FSIQ is an IQ assessed by measuring an individual's overall level of general cognitive and intellectual functioning.
The highest FSIQ is 160.
The greater the quotient, higher the level of intelligence.
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Baseline and Week 96
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Change From Baseline in NCFT: Controlled Oral Word Association Test at Week 96
時間枠：Baseline and Week 96
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The Controlled Oral Word Associated Test is a measure of verbal fluency, which requires participants to generate words orally that begin with a given letter of the alphabet.
Participants are given 1 min to name as many words as possible.
Performance was calculated by the number of words generated in the 1-min period.
This measure, requiring rapid and organized word retrieval, is a sensitive indicator of brain dysfunction.
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Baseline and Week 96
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Change From Baseline in NCFT: Rey Kim Memory Test-Korean Auditory Verbal Learning Test (KAVLT) at Week 96
時間枠：Baseline and Week 96
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The KAVLT is a neuropsychological assessment designed to evaluate verbal memory in participants.
The KAVLT is useful in evaluating the nature and severity of memory dysfunction and to track changes in memory function over time.
The test is designed as a list-learning paradigm in which the participants hears a list of 15 words, and are asked to recall as many words from the list as possible.
This procedure is carried out a total of 5 times.
Then a second list of 15 words is presented, allowing the participants only 1 attempt to recall.
Immediately following this, the participants are asked to remember as many words as possible from the first list.
KAVLT consists of 2 test conditions: Delayed Recall and Delayed Recognition.
The upper limit for 'words recalled' is 15, which represents better episodic memory.
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Baseline and Week 96
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Change From Baseline in NCFT: Rey Kim Memory Test- Korean-Rey Complex Figure Test (K-RCFT) at Week 96
時間枠：Baseline and Week 96
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The RCFT is a neuropsychological assessment designed to evaluate visual memory in participants.
The RCFT is useful in evaluating the spatial perception and visual memory.
The RCFT consists of 3 test conditions: Copy, Immediate Recall and Delayed Recall.
At the first step, participants are given the RCFT stimulus card, and then asked to draw the same figure.
Subsequently, they are instructed to draw what they remembered.
Then, after a delay of 30 min, they are required to draw the same figure once again, a score of 2 points for each drawn element (a complete straight line or a circle) remembered correctly.
The total score is the sum of points scored for each correctly drawn element and it ranges from 0 to 36.
The maximum score indicates excellent visual memory.
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Baseline and Week 96
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Change From Baseline in NCFT: Memory Quotient (MQ) at Week 96
時間枠：Baseline and Week 96
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MQ was obtained by adding up the results of verbal memory and visual memory test.
The memory quotient will include learning curve, memory retention, retrieval efficiency, drawing/memory consistency, verbal/visual memory consistency and intelligence/memory consistency.
The highest MQ is 160, which indicates excellent memory.
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Baseline and Week 96
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Change From Baseline in NCFT: Trail Making Test (TMT)-Time at Week 96
時間枠：Baseline and Week 96
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TMT is attention, mental flexibility, visual search, motor function measure test.
Test is divided into A and B types.
Participants using a pencil or connect numbers in sequence (A-type), in turn, alternating between numbers and letters must be connected (B-type).
The test measures the response time.
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Baseline and Week 96
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Change From Baseline in NCFT: TMT-Error at Week 96
時間枠：Baseline and Week 96
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TMT is attention, mental flexibility, visual search, motor function measure test.
Test is divided into A and B types.
Participants using a pencil or connect numbers in sequence (A-type), in turn, alternating between numbers and letters must be connected (B-type).
The test measures the the number of errors.
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Baseline and Week 96
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Liverpool University Neuroleptic Side Effect Rating Scale (LUNSERS) Score
時間枠：Baseline and Week 96
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The LUNSERS is a self-report measure of antipsychotic side effects.
It consists of 51 questions, 41 questions on side effects and 10 questions are of "red herrings" to validate the results.
Each question is rated on a 4-point scale, where 0=not at all; and 4=very much.
The total neuroleptic side effect score is the sum of the scores for the side effects items (i.e.
all items excluding the red herrings).
Total side effects score ranges from 0 to 164, where 0 to 40=low side effect rating, 41 to 80=medium side effect rating and greater than 81=high side effect rating.
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Baseline and Week 96
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Change From Baseline in Drug Attitude Inventory-10 (DAI-10) Item Scale Score at Week 96
時間枠：Baseline and Week 96
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The DAI-10 is a 10-item questionnaire to assess 1) subjective experience of medication and 2) attitudes and beliefs toward neuroleptics which may influence medication 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).
The final score for each person at each time is the positive score minus the negative score.
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Baseline and Week 96
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Total Drug Induced Extra-Pyramidal Symptoms Scale (DIEPSS) Score
時間枠：Baseline and Week 96
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A scale used to assess the extrapyramidal symptoms attributable to antipsychotics.
It consists of 9 items (8 to assess individual symptoms and 1 to assess global severity).
Each item is assessed from 0 (none, normal) to 4 (severe).
The total score is the sum of the 8 item scores, for a total range of 0 (normal) to 32 (severe).
The items for the assessment of individual symptoms are classified into 4 categories of parkinsonism, akathisia, dystonia and dyskinesia.
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Baseline and Week 96
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協力者と研究者
ここでは、この調査に関係する人々や組織を見つけることができます。
研究記録日
これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。
主要日程の研究
研究開始
2005年8月1日
一次修了 (実際)
2008年8月1日
研究の完了 (実際)
2008年8月1日
試験登録日
最初に提出
2005年12月22日
QC基準を満たした最初の提出物
2005年12月22日
最初の投稿 (見積もり)
2005年12月26日
学習記録の更新
投稿された最後の更新 (見積もり)
2014年4月16日
QC基準を満たした最後の更新が送信されました
2014年3月25日
最終確認日
2014年3月1日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。