Skip to main content
Clinical Trials/JPRN-UMIN000020527
JPRN-UMIN000020527RecruitingPhase 2

Multi-centered, placebo-controlled, double-blind, randomized clinical trial to assess the effect of oral inosine on the onset of wearing off in patients with early stage Parkinson's disease - Randomized clinical trial to assess the disease modifying effect of oral inosine for patients with Parkinson's disease

Ehime University Graduate School of Medicine0 sites100 target enrollmentStarted: February 1, 2016Last updated:
Conditions

Trial Snapshot

Phase
Phase 2
Status
Recruiting
Sponsor
Enrollment
100

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
20years-old to ot applicable (—)
Sex
All

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • A history of kidney stones, gout(or chronic arthritis), ischemic heart disease A history of kidney failure of eGFR <= 60 at the screening visit. Having uncontrolled hypertension which is defined as SBP>=160 or DBP >=100 Current treatment with medication which slows urate excretion, which is defined as taking diuretics, losartan, anti-tuberculosis drugs or immune-suppression agents. Being pregnant or having an intention to become pregnant during the study period. Other factors that investigators deem inappropriate to enroll for the trial. (e.g. Having malignancy, arthritis which is difficult to discern from gout, severe allergic history to drugs)

Investigators

Sponsor
Ehime University Graduate School of Medicine

Similar Trials

Active, not recruiting
Phase 1
A study to find out which dose of daridorexant is safe and effective to treat insomnia in children and adolescents 10 to <18 years oldInsomnia Disorder
EUCTR2021-003867-87-BEIdorsia Pharmaceuticals Ltd150
Active, not recruiting
Phase 1
A study to find out which dose of daridorexant is safe and effective to treat insomnia in children and adolescents 10 to <18 years oldInsomnia Disorder
EUCTR2021-003867-87-DEIdorsia Pharmaceuticals Ltd150
Completed
Phase 2
The efficacy of Homeopathic medicines in the prevention of COVID-19 in Quarantined or Exposed Individuals
CTRI/2020/05/025491ife Force Foundation Trust2,233
Active, not recruiting
Phase 1
Double-blind, Randomized, Multicenter, Placebo-Controlled, Parallel Group Study to Characterize the Efficacy, Safety, and Tolerability of 24 Weeks of Evolocumab for Low Density Lipoprotein-Cholesterol (LDL-C) Reduction, as Add-On to Diet and Lipid-Lowering Therapy, in Pediatric Subjects 10 to 17 Yearsof Age With Heterozygous Familial Hypercholesterolemia (HeFH)Heterozygous familial hypercholesterolaemiaMedDRA version: 18.0Level: LLTClassification code 10057079Term: Heterozygous familial hypercholesterolemiaSystem Organ Class: 100000004850
EUCTR2014-002277-11-ITAmgen Inc158
Active, not recruiting
Phase 1
Study to assess the long term safety and efficacy of evolocumab in children aged 10 to 17 years with Heterozygous Familial HypercholesterolemiaHeterozygous familial hypercholesterolemiaMedDRA version: 20.0Level: LLTClassification code 10057079Term: Heterozygous familial hypercholesterolemiaSystem Organ Class: 100000004850
EUCTR2014-002277-11-PTAmgen Inc150