This study will evaluate the therapeutic efficacy and safety of DA-9701 with domperidone in
patients with Parkinson's disease
Drug: Placebo domperidone
Drug: Placebo DA-9701
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Full eligibility criteria for NCT03022201
Ages eligible for Study
20 Years to 80 Years
Genders eligible for Study
Accepts Healthy Volunteers
subjects diagnosed with spontaneous parkinsonism by the United Kingdom(UK) Parkinson's Disease Society Brain Bank criteria
subjects who are able to explain symptoms they experience and to complete relevant assessment and exams including questionaires
subjects who understand the purpose and protocols of the study and agree to participate on the study
subjects who experience psychiatrical disorders such as cognitive or behavioral disorders
subjects who are on prokinetics or who are unable to cease such medication
subjects who present neurological disorders which influence gastrointestinal mobility
subjects who present gastrointestinal conditions which influence gastrointestinal mobility
subjects with a history of gastrectomy or colectomy
subjects who are unable to receive and complete the course of medication due to other metabolic disorders
subjects diagnosed with parkinson plus syndrome
subjects who are unable to undergo MRI scan for safety reasons due to claustrophobia or certain devices such as cardiac pacemakers or aneurysm clips
All locations for NCT03022201
Cheol Min Shin
View full eligibility
Tris trial is registered with FDA with number: NCT03022201. The sponsor of the trial is Seoul National University Hospital and it is looking for 40 volunteers for the current phase.
Official trial title: Therapeutic Efficacy of DA-9701 on Gastric Motility in Patients With Parkinson's Disease Evaluated by Magnetic Resonance Imaging: A Randomized Controlled, Double-Blind, Non-Inferiority Trial
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