Two-phase Randomized Controlled Trial of Low and Moderate Dose Methylphenidate for Non-motor and Postural Symptoms in Parkinson's Disease.
试验速览
- 阶段
- 4 期
- 状态
- 终止
- 入组人数
- 6
- 试验地点
- 2
- 主要终点
- Conners' Continuous Performance Test-II score
研究概览
简要总结
This project aims to determine if methylphenidate can improve deficits in attention and symptoms of orthostatic hypotension, two common non-motor symptoms, in patients with Parkinson's Disease. This project also seeks to evaluate the effect of methylphenidate on postural control in these patients, a debilitating motor symptom that places patients at an increased risk of falling. This study will build on existing data to support a new indication for the use of methylphenidate in Parkinson's Disease. Using standard and objective evaluations, this study will quantify the effect of methylphenidate at two doses on attention levels, orthostatic hypotension, and measures of postural control. Phase I of the study will compare methylphenidate 10mg three times daily to placebo and Phase II of the study, for those tolerating the lower dose in Phase I, will compare methylphenidate 20mg three times daily to placebo. By incorporating two different doses, the study also seeks to determine if any improvements are dose-related. Secondary endpoints will include safety assessments (adverse event monitoring and vital signs) performed every 30 minutes following supervised drug administration. Visual analog scales will be presented to each participant before treatment and following the final dose of each treatment to assess changes in fatigue. A secondary task will be added to postural tests to assess the influence of cognitive processes. It is hypothesized that methylphenidate will demonstrate a significant beneficial effect on all outcomes. It is projected that objective improvements will be observed following treatment with methylphenidate at both doses (10 and 20mg three time daily) when compared to placebo. It is further hypothesized that the effects will be dose-related and therefore more profound with higher doses.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Treatment
- 盲法
- Double (Participant, Outcomes Assessor)
入排标准
- 年龄范围
- — 至 75 Years（Child, Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patients with stages 2-3 Parkinson's disease as defined by the Hoehn &Yahr staging system (Hoehn &Yahr, 1967).
- •Age less than or equal to 75 years.
- •Subjects who are willing and able to provide, in writing, informed consent.
- •Subjects who are willing and able to be confined to the clinical research unit as required by the protocol and to complete all procedures required on an outpatient basis.
排除标准
- •Subjects with evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurological, or allergic disease (including drug allergies and excluding seasonal allergies).
- •Subjects with a history of substance abuse or dependence or a positive urine screen for drugs of abuse.
- •A history of regular alcohol consumption exceeding 7 drinks/week for women or 14 drinks/week for men (1 drink = 5 ounces of wine or 12 ounces of beer or 1.5 ounces of hard liquor) within 6 months of screening.
- •Subjects with a documented allergy to methylphenidate or one of the product excipients.
- •Subjects with any medical condition affecting drug absorption (e.g. gastrectomy).
- •Treatment with an investigational drug within 30 days or 5 half-lives (whichever is longer) preceding the first dose of study medication.
- •Use of a monoamine oxidase inhibitor or other interacting medication within the preceding 14 days or 5 half-lives (whichever is longer).
- •History of sensitivity to heparin or heparin-induced thrombocytopenia.
研究组 & 干预措施
Methylphenidate 10
Methylphenidate 10mg three times daily for a total of 7 doses.
干预措施: Methylphenidate (Drug)
Placebo 10
Placebo capsule three times daily for a total of 7 doses.
干预措施: Placebo 10 (Drug)
Methylpheindate 20
Methylphenidate 20mg three times daily for a total of 7 doses.
干预措施: Methylphenidate (Drug)
Placebo 20
Placebo capsule three times daily for a total of 7 doses.
干预措施: Placebo 20 (Drug)
结局指标
主要结局
Conners' Continuous Performance Test-II score
时间窗: Baseline, 2 hours following first dose, 2 hours following last dose
Orthostatic drop - blood pressure in mmHg
时间窗: Baseline, 2 hours following first dose, 2 hours following last dose
Blood pressure will be measured following 5 minutes of rest in a lying position and again 1, 3, and 5 minutes after rising to a standing position. The orthostatic drop will be calculated by subtracting the blood pressures recorded at each time interval(1, 3, and 5 minutes after standing) from the blood pressure recorded in a lying position.
Average speed of center of pressure oscillations
时间窗: Baseline, 2 hours following first dose, 2 hours following last dose
As recorded using dynamic posturography (Sensory Organization Test).
Total area of center of pressure oscillations
时间窗: Baseline, 2 hours following first dose, 2 hours following last dose
As recorded using dynamic posturography (Sensory Organization Test).
次要结局
- Visual analog fatigue scale scores(Baseline, 2 hours following last dose)
- Blood pressure (mmHg)(Baseline, 30, 60, and 90 minutes following first and final dose of study medication)
- Heart rate(Basesline, 30, 60, and 90 minutes following first and final dose of study medication)
- Number of errors recorded for 'Backward Digit Span' task(Baseline, 2 hours following first dose, 2 hours following final dose)