Treating H. Pylori in Parkinson's Patients With Motor Fluctuations
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| ClinicalTrials.gov Identifier: NCT00664209 |
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Recruitment Status :
Terminated
(Prevalence of H Pylori in the study population was much lower than anticipated)
First Posted : April 22, 2008
Results First Posted : December 2, 2017
Last Update Posted : December 2, 2017
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| Condition or disease | Intervention/treatment | Phase |
|---|---|---|
| Parkinson's Disease Helicobacter Infections Motor Fluctuations | Drug: clartihromycin, amoxicillin, and omeprazole Drug: placebo | Phase 3 |
| Study Type : | Interventional (Clinical Trial) |
| Actual Enrollment : | 64 participants |
| Allocation: | Randomized |
| Intervention Model: | Parallel Assignment |
| Masking: | Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor) |
| Primary Purpose: | Treatment |
| Official Title: | Helicobacter Pylori Eradication and Motor Fluctuations in Parkinson's Disease |
| Study Start Date : | January 2008 |
| Actual Primary Completion Date : | June 2011 |
| Actual Study Completion Date : | June 2012 |
| Arm | Intervention/treatment |
|---|---|
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Active-placebo
These subject receive treatment with active triple therapy followed by treatment with placebo therapy.
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Drug: clartihromycin, amoxicillin, and omeprazole
clarithromycin 500mg - i PO BID x10 days; amoxicillin 1gm - i PO BID x10 days; omeprazole 10mg - i PO BID x10 days
Other Name: Biaxin, Prilosec Drug: placebo placebo therapy |
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Placebo-active
These subject receive treatment with placebo therapy followed by treatment with active triple therapy.
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Drug: clartihromycin, amoxicillin, and omeprazole
clarithromycin 500mg - i PO BID x10 days; amoxicillin 1gm - i PO BID x10 days; omeprazole 10mg - i PO BID x10 days
Other Name: Biaxin, Prilosec Drug: placebo placebo therapy |
- "Off" Time [ Time Frame: 2 months ]Average total daily "off" time (measured by patient symptom diaries) in hours
- Improvement in UPDRS Total Scores [ Time Frame: 2 months ]The Unified Parkinson Disease Rating Scale (UPDRS) is a rating tool to follow the longitudinal course of Parkinson's Disease. It is made up of the 1) Mentation, Behavior, and Mood, 2) ADL and 3) Motor sections. These are evaluated by interview. Some sections require multiple grades assigned to each extremity. A total of 199 points are possible. 199 represents the worst (total) disability), 0--no disability.
- Improvement in UDPRS Part III [ Time Frame: 2 months ]Improvement in UDPRS Part III (Motor) scores ("on" and "off") UPDRS III is the result of a motor examination with the scores 0-108. A decrease in the scores means improvement
- Improvement in Quality of Life as Assessed by PDQ-39 [ Time Frame: 2 months ]The Parkinson's Disease Questionnaire (PDQ)-39 contains 39 questions addressing how often patients have experienced difficulties due to having PD in the preceding month. Items are scored from 0 (never) to 4 (always). Lower scores indicate better quality of life.
- Participants With Side Effects From Study Treatment [ Time Frame: 2 months ]Side effects profile
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| Ages Eligible for Study: | Child, Adult, Older Adult |
| Sexes Eligible for Study: | Male |
| Accepts Healthy Volunteers: | No |
Inclusion criteria:
- Adults diagnosed with idiopathic Parkinson's disease, Hoehn & Yahr stage 2-4 in the "off" state, with no other concomitant neurologic diseases.
- Stable (≥30 days) Parkinson's disease therapy, with demonstrable medication efficacy, but with wearing off phenomenon present between levodopa doses (average off time ≥3 hours off time/day).
- Levodopa therapy required; Any formulation (e.g. Sinemet, Sinemet CR, Stalevo) is acceptable. Parkinson's disease treatment may also include any of the following medications or classes: non-ergot dopamine agonists, COMT inhibitors, MAO-B inhibitors, amantadine, anticholinergics.
- Positive for H. pylori IgG Ab by serum ELISA (before inclusion in randomized treatment arms).
Exclusion criteria:
- Current abdominal pain, unexplained nausea/vomiting, or gastrointestinal bleeding.
- History of gastric cancer, peptic ulcer, duodenal ulcer, or other gastric or duodenal lesions.
- History of previous gastric surgery.
- History of previous brain surgery for Parkinson's disease.
- Family history of gastric cancer.
- Prior treatment for H. pylori+ status.
- Recent use (previous 4 weeks) of proton-pump inhibitor, amoxicillin, or clarithromycin.
- Allergy or sensitivity to penicillin, amoxicillin, clarithromycin, or omeprazole.
- Use of drugs affecting gastric motility (e.g. domperidone, metoclopramide).
- Inability to tolerate or participate in testing in the morning in an "off" state.
- Inability to communicate effectively with study personnel in English.
- Pregnancy.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00664209
| United States, California | |
| UCLA Neurology | |
| Los Angeles, California, United States, 90095 | |
| Principal Investigator: | Jeff M Bronstein, MD, PhD | UCLA Neurology |
| Responsible Party: | Jeff Bronstein, Professor of Neurology, University of California, Los Angeles |
| ClinicalTrials.gov Identifier: | NCT00664209 |
| Other Study ID Numbers: |
MJJF Clinical Discovery 2007 441437-JB-58330 |
| First Posted: | April 22, 2008 Key Record Dates |
| Results First Posted: | December 2, 2017 |
| Last Update Posted: | December 2, 2017 |
| Last Verified: | October 2017 |
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Parkinson's disease levodopa Helicobacter pylori |
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Helicobacter Infections Parkinson Disease Parkinsonian Disorders Basal Ganglia Diseases Brain Diseases Central Nervous System Diseases Nervous System Diseases Movement Disorders Synucleinopathies Neurodegenerative Diseases Gram-Negative Bacterial Infections Bacterial Infections |
Bacterial Infections and Mycoses Infections Amoxicillin Omeprazole Anti-Bacterial Agents Anti-Infective Agents Anti-Ulcer Agents Gastrointestinal Agents Proton Pump Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action |

