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Helicobacter Pylori Eradication Study in Parkinson's Disease

Primary Purpose

Parkinson's Disease, Helicobacter Pylori Infection

Status
Completed
Phase
Not Applicable
Locations
Malaysia
Study Type
Interventional
Intervention
Helicobacter pylori eradication therapy
Placebo
Sponsored by
University of Malaya
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Parkinson's Disease focused on measuring Parkinson's Disease, Helicobacter pylori infection

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • University of Malaya

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Helicobacter pylori eradication therapy

Placebo

Arm Description

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

Maltodextrin

Outcomes

Primary Outcome Measures

"On-medication" MDS-UPDRS Part III score

Secondary Outcome Measures

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

Full Information

First Posted
April 4, 2014
Last Updated
October 28, 2019
Sponsor
University of Malaya
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1. Study Identification

Unique Protocol Identification Number
NCT02108704
Brief Title
Helicobacter Pylori Eradication Study in Parkinson's Disease
Official Title
Helicobacter Pylori Eradication in Parkinson's Disease: A Double-blind Randomised Placebo Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Completed
Study Start Date
December 2013 (undefined)
Primary Completion Date
December 2015 (Actual)
Study Completion Date
May 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Malaya

4. Oversight

Data Monitoring Committee
No

5. Study Description

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).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson's Disease, Helicobacter Pylori Infection
Keywords
Parkinson's Disease, Helicobacter pylori infection

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
75 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Helicobacter pylori eradication therapy
Arm Type
Active Comparator
Arm Description
Amoxycillin 1gm twice a day (BD) Clarithromycin 500mg BD Omeprazole 20mg BD
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Maltodextrin
Intervention Type
Drug
Intervention Name(s)
Helicobacter pylori eradication therapy
Intervention Type
Drug
Intervention Name(s)
Placebo
Primary Outcome Measure Information:
Title
"On-medication" MDS-UPDRS Part III score
Time Frame
at 3 months after randomisation
Secondary Outcome Measure Information:
Title
"On-medication" UPDRS Part III score
Time Frame
at 1 year post randomisation
Title
"On-medication" Pegboard Score
Time Frame
at 3 months and 1 year post randomisation
Title
"On-medication" Timed Gait Score
Time Frame
at 3 months and 1 year post randomisation
Title
Parkinson's Kinetigraph (PKG) Bradykinesia and Dyskinesia Scores
Time Frame
at 3 months and 1 year post randomisation
Title
UPDRS Part IV
Time Frame
at 3 months and 1 year post randomisation
Title
UPDRS Part II
Time Frame
at 3 months and 1 year post randomisation
Title
UPDRS Part I
Time Frame
at 3 months and 1 year post randomisation
Title
Montreal Cognitive Assessment Score
Time Frame
at 3 months and 1 year post randomisation
Title
Leeds Dyspepsia Questionnaire
Time Frame
at 3 months and 1 year post randomisation
Title
Parkinson Disease Questionnaire (PDQ-39)
Time Frame
at 3 months and 1 year post randomisation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ai Huey Tan, MD,MRCP(UK)
Organizational Affiliation
University of Malaya
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Malaya
City
Kuala Lumpur
State/Province
Wilayah Persekutuan
ZIP/Postal Code
59100
Country
Malaysia

12. IPD Sharing Statement

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Helicobacter Pylori Eradication Study in Parkinson's Disease

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