The Effect of Methylphenidate on Non-motor Symptoms and Postural Control in Parkinson's Disease.

Parkinson's Disease Clinical Trial

Official title:

Two-phase Randomized Controlled Trial of Low and Moderate Dose Methylphenidate for Non-motor and Postural Symptoms in Parkinson's Disease.

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT01244269
• Other study ID #: MPH.NMS.2011
• Status: Terminated
• Phase: Phase 4
• First received: November 18, 2010
• Last updated: October 19, 2012
• Start date: December 2010
• Est. completion date: June 2011

Study information

• Verified date: October 2012
• Source: Laval University
• Contact: n/a
• Is FDA regulated: No
• Health authority: Canada: Health Canada
• Study type: Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 6
• Est. completion date: June 2011
• Est. primary completion date: June 2011
• Accepts healthy volunteers: No
• Gender: Both
• Age group: N/A to 75 Years

Eligibility

Inclusion Criteria:

• 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.

Exclusion Criteria:

• 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.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Parkinson Disease
• Parkinson's Disease

Intervention

Drug:
• Methylphenidate
Methylphenidate 10mg tablets will be overencapsulated in gelatin capsules for blinding. Subjects will take 1 capsule three times daily for a total of 7 doses.
• Methylphenidate
Methylphenidate 20mg three times daily for a total of 7 doses.
• Placebo 10
Blind gelatin capsule three times daily for a total of 7 doses.
• Placebo 20
Blind gelatin capsule three times daily for a total of 7 doses

Locations

Country	Name	City	State
Canada	Laval University	Québec	Quebec
Canada	Québec Memory and Motor Skills Disorders Research Center	Québec	Quebec

Sponsors (3)

Lead Sponsor	Collaborator
Laval University	Fonds de la Recherche en Santé du Québec, Quebec Memory and Motor Skills Disorders Research Center

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Conners' Continuous Performance Test-II score		Baseline, 2 hours following first dose, 2 hours following last dose	No
Primary	Orthostatic drop - blood pressure in mmHg	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.	Baseline, 2 hours following first dose, 2 hours following last dose	No
Primary	Average speed of center of pressure oscillations	As recorded using dynamic posturography (Sensory Organization Test).	Baseline, 2 hours following first dose, 2 hours following last dose	No
Primary	Total area of center of pressure oscillations	As recorded using dynamic posturography (Sensory Organization Test).	Baseline, 2 hours following first dose, 2 hours following last dose	No
Secondary	Visual analog fatigue scale scores		Baseline, 2 hours following last dose	No
Secondary	Blood pressure (mmHg)		Baseline, 30, 60, and 90 minutes following first and final dose of study medication	Yes
Secondary	Heart rate		Basesline, 30, 60, and 90 minutes following first and final dose of study medication	Yes
Secondary	Number of errors recorded for 'Backward Digit Span' task	Following administration of the Backward Digit Span assessment of the Wechsler Adult Intelligence Scale to control for individual capacities, each subject will be provided with a string of digits before the onset of 50% of the trials in the postural test. Subjects will be required to memorize the string of digits in reverse and repeat them at the end of the trial. Errors will be quantified as either errors of insertion, deletion, or order.	Baseline, 2 hours following first dose, 2 hours following final dose	No