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Dopamine Precursor

L-dopa for Parkinson's Disease

Phase 2
Waitlist Available
Led By Alfonso Fasano, MD, PhD
Research Sponsored by University of Toronto
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 months
Awards & highlights

Study Summary

Deep Brain Stimulation (DBS) of the Subthalamic nucleus (STN) is an established treatment for patients with advanced Parkinson's disease (PD). STN DBS improves dopaminergic drug-responsive motor symptoms, thus allowing a reduction of post-operative drug dose. However, a considerable variation in the extent of dopaminergic drug reduction has been reported, with values ranging from 20% to 100%. Both L-dopa and DAs can be used, however, there are no formal studies examining which type of antiparkinsonian medication may be more effective and/or better tolerated following STN DBS. Aim of our study is to compare the efficacy and the tolerability of L-dopa monotherapy versus DAs monotherapy after STN DBS over a 3-month follow up period. This study is a prospective, single blind parallel trial comparing L-dopa monotherapy and DAs monotherapy after STN DBS. Patients will be enrolled in pairs, with one patient randomly assigned to L-dopa monotherapy and the other to DA monotherapy after STN DBS (20 patients for each study arm). Treatment assignment will be unmasked for the patient but will be blinded for the neurologist programming DBS and evaluating the patient. Another neurologist will be in charge of medication adjustments. Primary outcome is the change in severity of non-motor symptoms as assessed by the Non-motor Symptoms Scale (NMSS) at 3-month follow up visit after surgery. In spite of an improvement of the motor condition many patients develop apathy and depression following surgery ("Neurosurgery in Parkinson's disease: the doctor is happy, the patient less so"). This study will shed light on the best way to manage patients after STN procedure, thus contributing to a further improvement of the surgical outcome in a population of young and motivated patients (those commonly receiving STN DBS), eventually bringing them closer to a normal personal and social life. Results of our study may provide new insights in the management of advanced PD after STN DBS, further leading to development of future larger trials.

Eligible Conditions
  • Parkinson's Disease

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 3 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Severity at 3-month follow up visit after surgery of non-motor symptoms as assessed by the Non-motor Symptoms Scale (NMSS)
Secondary outcome measures
Safety and tolerability will be assessed by recording the frequency and the severity of reported adverse events during each visit.
activities of daily living as assessed by the MDS Unified Parkinson's Disease Rating Scale, Activities of daily living section (MDS-UPDRS-II)
• motor fluctuations and dyskinesias as assessed by the MDS Unified Parkinson's Disease Rating Scale, part IV (MDS- UPDRS-IV)
+5 more

Side effects data

From 2014 Phase 4 trial • 127 Patients • NCT01770145
20%
Nausea
8%
Yawning
6%
Somnolence
5%
Chills
5%
Vomiting
3%
Flushing
2%
Fatigue
2%
Hyperhidrosis
2%
Headache
2%
Oedema
2%
Urinary Tract Infection
2%
Feeling hot
2%
Chest Discomfort
2%
Pallor
2%
Hypotension
1%
Sneezing
1%
Vertigo
1%
Injection site erythema
1%
Confusional state
1%
Rhinitis
1%
Retching
1%
Eyelid ptosis
1%
Eye pain
1%
Dyspnoea
1%
Hiccups
1%
Vision blurred
1%
Paraesthesia
1%
Diplopia
1%
Erythema
1%
Tinnitus
1%
Palpitations
1%
Injection Site Pruritus
1%
Pain in jaw
1%
Restlessness
1%
Chest Pain
1%
Hot flush
1%
Sinus Congestion
1%
Cold sweat
1%
Rhinorrhoea
1%
Delusion
1%
Nasal Congestion
1%
Ocular hyperaemia
1%
Neck pain
1%
Hyposaethesia
1%
Dysgeusia
1%
Toothache
1%
Salivary hyper-secretion
1%
Ear Pain
1%
Stress Fracture
1%
Joint Sprain
1%
Fall
1%
Contusion
1%
Dyskinesia
1%
Mobility decreased
1%
Limb discomfort
1%
Heart rate increased
1%
Orthostatic hypotension
100%
80%
60%
40%
20%
0%
Study treatment Arm
APOKYN

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: L-dopaExperimental Treatment1 Intervention
L-dopa will be administered as monotherapy. The dosage and the frequency of intakes are not pre-specified and will be individualized.
Group II: Dopamine agonistActive Control1 Intervention
Dopamine agonists (either pramipexole or ropirinole) will be administered as monotherapy. The dosage and the frequency of intakes are not pre-specified and will be individualized.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Levodopa
FDA approved

Find a Location

Who is running the clinical trial?

Michael J. Fox Foundation for Parkinson's ResearchOTHER
112 Previous Clinical Trials
535,081 Total Patients Enrolled
University of TorontoLead Sponsor
690 Previous Clinical Trials
1,019,603 Total Patients Enrolled
Alfonso Fasano, MD, PhDPrincipal InvestigatorMovement Disorders Centre Toronto Western Hospital
3 Previous Clinical Trials
88 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
~4 spots leftby May 2025