Parkinson's Disease Clinical Trial
Official title:
Helicobacter Pylori Eradication in Parkinson's Disease: A Double-blind Randomised Placebo Controlled Trial
NCT number | NCT02108704 |
Other study ID # | HPPD |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | December 2013 |
Est. completion date | May 2016 |
Verified date | October 2019 |
Source | University of Malaya |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
It has been hypothesized, based on epidemiological observations, that Helicobacter pylori (HP) infection may play a role in the pathogenesis of Parkinson's Disease (PD). Previous studies have also shown that HP eradication therapy may result in improvements in levodopa pharmacokinetics and motor fluctuations. This study aims to examine the effects of HP eradication, using a double-blind randomized placebo-controlled trial design in a relatively large cohort of patients. Outcomes of interest include motor function, gastrointestinal symptoms and health-related quality of life. The investigators hypothesize that HP eradication will lead to improvements in motor function. The primary outcome of interest is the "ON"-medication Unified PD Rating Scale (UPDRS) Part III score at 3 months. Secondary outcomes include Purdue Pegboard Score, Timed Test of Gait, Dyskinesia and Bradykinesia scores measured by Parkinson's Kinetigraph (PKG), Leeds Dyspepsia Questionnaire (LDQ), Parkinson's Disease Questionnaire (PDQ-39), UPDRS Part I, Part II and Part IV; and Montreal Cognitive Assessment (MOCA).
Status | Completed |
Enrollment | 75 |
Est. completion date | May 2016 |
Est. primary completion date | December 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: 1. Aged =18 years 2. Provision of written informed consent 3. Clinical diagnosis of Parkinson's Disease (PD) assigned by a consultant neurologist Exclusion Criteria: 1. History of previous gastric or major abdominal/pelvic surgery 2. History of previous eradication therapy for Helicobacter pylori 3. Antibiotic use in the preceding four weeks or use of anti-acid/prokinetics/laxatives in the preceding one week prior to breath test 4. Recent initiation of dopaminergic medications (within the last three months) or recent adjustment of dopaminergic medications (within the last one month) 5. History of functional neurosurgery for PD 6. No concomitant neurologic disease except PD 7. Medical condition that prevents reliable completion of questionnaire |
Country | Name | City | State |
---|---|---|---|
Malaysia | University of Malaya | Kuala Lumpur | Wilayah Persekutuan |
Lead Sponsor | Collaborator |
---|---|
University of Malaya |
Malaysia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | "On-medication" MDS-UPDRS Part III score | at 3 months after randomisation | ||
Secondary | "On-medication" UPDRS Part III score | at 1 year post randomisation | ||
Secondary | "On-medication" Pegboard Score | at 3 months and 1 year post randomisation | ||
Secondary | "On-medication" Timed Gait Score | at 3 months and 1 year post randomisation | ||
Secondary | Parkinson's Kinetigraph (PKG) Bradykinesia and Dyskinesia Scores | at 3 months and 1 year post randomisation | ||
Secondary | UPDRS Part IV | at 3 months and 1 year post randomisation | ||
Secondary | UPDRS Part II | at 3 months and 1 year post randomisation | ||
Secondary | UPDRS Part I | at 3 months and 1 year post randomisation | ||
Secondary | Montreal Cognitive Assessment Score | at 3 months and 1 year post randomisation | ||
Secondary | Leeds Dyspepsia Questionnaire | at 3 months and 1 year post randomisation | ||
Secondary | Parkinson Disease Questionnaire (PDQ-39) | at 3 months and 1 year post randomisation |
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