Skip to main content
Clinical Trials/NCT02108704
NCT02108704CompletedNot Applicable

Helicobacter Pylori Eradication in Parkinson's Disease: A Double-blind Randomised Placebo Controlled Trial

University of Malaya1 site in 1 country75 target enrollmentStarted: December 2013Last updated:
Conditions
Interventions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
75
Locations
1
Primary Endpoint
"On-medication" MDS-UPDRS Part III score

Study Overview

Brief Summary

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).

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Aged ≥18 years
  • Provision of written informed consent
  • Clinical diagnosis of Parkinson's Disease (PD) assigned by a consultant neurologist

Exclusion Criteria

  • History of previous gastric or major abdominal/pelvic surgery
  • History of previous eradication therapy for Helicobacter pylori
  • Antibiotic use in the preceding four weeks or use of anti-acid/prokinetics/laxatives in the preceding one week prior to breath test
  • Recent initiation of dopaminergic medications (within the last three months) or recent adjustment of dopaminergic medications (within the last one month)
  • History of functional neurosurgery for PD
  • No concomitant neurologic disease except PD
  • Medical condition that prevents reliable completion of questionnaire

Arms & Interventions

Helicobacter pylori eradication therapy

Active Comparator

Amoxycillin 1gm twice a day (BD) Clarithromycin 500mg BD Omeprazole 20mg BD

Intervention: Helicobacter pylori eradication therapy (Drug)

Placebo

Placebo Comparator

Maltodextrin

Intervention: Placebo (Drug)

Outcomes

Primary Outcomes

"On-medication" MDS-UPDRS Part III score

Time Frame: at 3 months after randomisation

Secondary Outcomes

  • "On-medication" UPDRS Part III score(at 1 year post randomisation)
  • UPDRS Part IV(at 3 months and 1 year post randomisation)
  • UPDRS Part II(at 3 months and 1 year post randomisation)
  • UPDRS Part I(at 3 months and 1 year post randomisation)
  • "On-medication" Pegboard Score(at 3 months and 1 year post randomisation)
  • "On-medication" Timed Gait Score(at 3 months and 1 year post randomisation)
  • Parkinson's Kinetigraph (PKG) Bradykinesia and Dyskinesia Scores(at 3 months and 1 year post randomisation)
  • Montreal Cognitive Assessment Score(at 3 months and 1 year post randomisation)
  • Leeds Dyspepsia Questionnaire(at 3 months and 1 year post randomisation)
  • Parkinson Disease Questionnaire (PDQ-39)(at 3 months and 1 year post randomisation)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials