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NWP09 in Children With Attention Deficit Hyperactivity Disorder (ADHD)

2016年1月4日 更新者:Pfizer

A Multicenter, Dose-optimized, Double-blind, Randomized, Placebo-controlled Study To Evaluate The Efficacy Of Nwp09 In Pediatric Patients With Attention Deficit Hyperactivity Disorder (Adhd) In A Laboratory Classroom

The safety and efficacy of a chewable formulation of extended-release methylphenidate will be studied in children with ADHD

調査の概要

研究の種類

介入

入学 (実際)

90

段階

  • フェーズ 3

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

    • Arkansas
      • Little Rock、Arkansas、アメリカ、72211
        • Clinical Study Centers, LLC
    • California
      • Huntington Beach、California、アメリカ、92646
        • Laboratory School
      • Irvine、California、アメリカ、92612
        • UC Irvine Child Development Center
      • Irvine、California、アメリカ、92697
        • UC Irvine - Hewitt Hall
    • Florida
      • Bradenton、Florida、アメリカ、34201
        • Florida Clinical Research Center, LLC
      • Bradenton、Florida、アメリカ、34202
        • Woodland Community Church (Laboratory School)
    • Nevada
      • Las Vegas、Nevada、アメリカ、89128
        • Center for Psychiatry and Behavioral Medicine, Inc.
    • Texas
      • Houston、Texas、アメリカ、77007
        • Bayou City Research, Ltd.
      • Lubbock、Texas、アメリカ、79423
        • Westex Clinical Investigations

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

6年~12年 (子)

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:

  • Children aged 6 to 12 years with ADHD who require pharmacologic treatment for this condition

Exclusion Criteria:

  • Other serious illnesses or conditions that would put the patient at particular risk for safety events or would interfere with treatment/assessment of ADHD

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:ランダム化
  • マスキング:4倍

武器と介入

参加者グループ / アーム
介入・治療
プラセボコンパレーター:プラセボ
プラセボ
実験的:Active
NWP09
Methylphenidate, variable dose, daily dosing, 1 week duration

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
Swanson, Kotin, Agler, M-Flynn, and Pelham Rating Scale (SKAMP)-Combined Scores-Average of All Post-Dose Time-Points
時間枠:0.75 up to 13 hours post-dose
The SKAMP scale measured the manifestations of attention deficit hyperactivity disorder (ADHD) using an independent observer rating of the participant's impairment in classroom observed behaviors. SKAMP combined score comprised of 13 items (including subscales: attention with items 1-4, deportment with items 5-8, quality of work with items 9-11 and compliance with items 12-13). The SKAMP composite score was obtained by summing up each item score where each item was rated on a 7-point impairment scale (0=normal to 6=maximal impairment) for a total possible combined score of 0 to 78; where higher score signified worst impairment. Average of all post dose SKAMP-combined scores measured at 0.75, 2, 4, 8, 10, 12 and 13 hours post-dose was calculated.
0.75 up to 13 hours post-dose

二次結果の測定

結果測定
メジャーの説明
時間枠
Onset and Duration of Clinical Effect
時間枠:0.75, 2, 4, 8, 10, 12, 13 hours post-dose
Onset and duration of clinical effect was determined using SKAMP combined rating scale at each post-dose time point. Onset of effect was defined as first assessment time showing statistical significance (i.e. p was less than or equal to [=<] 0.05) between NWP09 and placebo and duration of effect was defined as the as last consecutive time-point at which difference was statistically significant between NWP09 and placebo. SKAMP scale measured the manifestations of ADHD using an independent observer rating of the participant's impairment in classroom observed behaviors. SKAMP combined score was comprised of 13 items [subscales: attention (1-4 items), deportment (5-8 items), quality of work (9-11 items) and compliance (12-13 items)]. SKAMP combined score was obtained by summing up each item score where each item was rated on a 7-point impairment scale (0=normal to 6=maximal impairment) for total possible combined score of 0 to 78; where higher score signified worst impairment.
0.75, 2, 4, 8, 10, 12, 13 hours post-dose
Swanson, Kotin, Agler, M-Flynn, and Pelham Rating Scale (SKAMP) SKAMP Attention and Deportment Subscale Scores at Hour 0.75, 2, 4, 8, 10, 12 and 13 Post-Dose
時間枠:0.75, 2, 4, 8, 10, 12, 13 hours post-dose
SKAMP scale measured the manifestations of ADHD using an independent observer rating of the participant's impairment in classroom observed behaviors. The SKAMP subscales were obtained by summing the individual items as follows: Attention (items 1-4) and Deportment (items 5-8), where each item was rated on a 7-point scale (0=normal to 6=maximal impairment). SKAMP attention subscale was reported which evaluates concentration in the classroom and comprises of 4 items, with a total possible score for of 0 to 24; higher score indicates worst impairment. SKAMP deportment subscale was reported which assesses behavior in the classroom and comprises of 4 items, with a total possible score for each sub-scale of 0 to 24; higher score indicates worst impairment.
0.75, 2, 4, 8, 10, 12, 13 hours post-dose
Permanent Product Measure of Performance (PERMP) Scores at Hour 0.75, 2, 4, 8, 10, 12 and 13 Post-Dose
時間枠:0.75, 2, 4, 8, 10, 12 and 13 post-dose
The PERMP score measured the manifestations of attention deficit hyperactivity disorder. The PERMP is a 10-minute written test, on 80 math problems, performed as seatwork in the classroom. At the end of the 10- minute math test , the PERMP score of the number of math problems attempted plus the number of math problems answered correctly in a 10-minute session was used to measure participant's performance. The total score range from 0-160 with higher scores indicating better performance.
0.75, 2, 4, 8, 10, 12 and 13 post-dose

その他の成果指標

結果測定
メジャーの説明
時間枠
Clinical Global Impression of Severity (CGI-S)
時間枠:Baseline, Day 8, 15, 22, 29, 36, 43
CGI-S scale was used to measure features associated with ADHD. The assessment was performed by the investigator of the study research team. The CGI-S classified the participant's current disease status as: 1 = normal, not at all ill, 2 = borderline ill, 3 = mildly ill, 4 = moderately ill, 5 = markedly ill, 6 = severely ill, and 7 = among the most extremely ill participants. This outcome measure was analyzed during open label phase in entire study population prior to randomization into two treatment groups.
Baseline, Day 8, 15, 22, 29, 36, 43
Clinical Global Impression-Improvement (CGI-I)
時間枠:Day 8, 15, 22, 29, 36, 43
The CGI-I measured the participant's disease improvement relative to baseline as followed: 1= very much improved, 2=much improved, 3=minimally improved, 4=no change, 5=minimally worse, 6= much worse, and 7=very much worse. This outcome measure was analyzed during open label phase in entire study population prior to randomization into two treatment groups.
Day 8, 15, 22, 29, 36, 43
Conners Parent Rating Scale (CPRS) Scores
時間枠:Baseline, Day 8, 15, 22, 29, 36, 43
CPRS was used to measure features associated with ADHD and was used to compare scores during the dose optimization period i.e. 1-6 weeks. The assessment was performed by parent or guardian. CPRS consisted of 27 questions graded on a scale from 0 (not true at all) to 3 (very much true). Raw scores were converted to t-scores and t-scores have a mean of 50 ± 10 where higher scores are indicative of greater problems. The participant received normalized t-scores on the following scales: oppositional, cognitive problems/inattention, hyperactivity, anxious-shy, perfectionism, social problems, psychosomatic, ADHD index, restless-impulse, emotional liability, conner's global index, inattentive, hyperactive-impulsive and diagnostic and statistical manual of mental disorders IV (DSM-IV). This outcome measure was analyzed during open label phase in entire study population prior to randomization into two treatment groups.
Baseline, Day 8, 15, 22, 29, 36, 43

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。

スポンサー

出版物と役立つリンク

研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

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

2012年7月1日

一次修了 (実際)

2012年10月1日

研究の完了 (実際)

2012年10月1日

試験登録日

最初に提出

2012年4月27日

QC基準を満たした最初の提出物

2012年7月26日

最初の投稿 (見積もり)

2012年7月31日

学習記録の更新

投稿された最後の更新 (見積もり)

2016年2月3日

QC基準を満たした最後の更新が送信されました

2016年1月4日

最終確認日

2016年1月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • NWP09-ADHD-300
  • B7491005 (その他の識別子:Alias Study Number)

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。

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