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| Name | Class |
|---|---|
| Daewoong Pharmaceutical Co. LTD. | INDUSTRY |
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This study aimed to investigate the efficacy of probiotics as a preventive agent for NSAID-induced enteropathy. Arthritis patients are randomly divided into probiotic and placebo groups, and the drug is administered for eight weeks. Before and after drug administration, the patient's symptoms/degree of small bowel injuries on capsule endoscopy/microbiome composition and diversity were investigated.
Background:
Due to aging, there are many long-term users of NSAIDs, increasing enteropathy. The prophylactic effect of misoprostol, which is currently used, has not been proven, and misoprostol's long-term compliance and safety remain questionable. Rebamipide shows insignificant effects in both treatment and prophylaxis.
Probiotics have been reported to affect enteropathy in animal and human studies. However, there needs to be more verification studies, and there needs to be confirmatory studies on the importance of the microbiome in the small bowel. However, it is expected that there will be fewer complications and less patient resistance, resulting in higher drug compliance.
Purpose: To identify the efficacy of probiotics on NSAID-induced enteropathy in arthritis patients by capsule endoscopy and questionnaire, and to analysis the composition and diversity of the microbiome
Design: Double-blinded randomized controlled, pilot study
Participant: Patients diagnosed with osteoarthritis and starting NSAIDs
Methods: Randomly administering Probiotics or Placebo for eight weeks and comparing "before and after administration" in arthritis patients
Outcome
Primary outcome: To assess whether probiotics can reduce small bowel injuries caused by NSAIDs
Secondary outcome:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Probiotics arm | Active Comparator | Probiotics combination capsule (Bacillus Subtilis 150 mg /Clostridium Burtyricum Toa 150 mg /Saccharomyces Boulardii 113 mg) per oral, three times a day, for 8 weeks |
|
| Placebo arm | Placebo Comparator | Placebo capsule in the same form as probiotics, per oral, three times a day, for 8 weeks |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Probiotics capsule | Combination Product | Subjects will take a probiotics combination capsule (Bacillus Subtilis 150 mg /Clostridium Burtyricum Toa 150 mg /Saccharomyces Boulardii 113 mg) three times a day for 8 weeks in combination with NSAIDs |
| Measure | Description | Time Frame |
|---|---|---|
| Changes in the small bowel injuries on capsule endoscopy | Changes in the number of ulcers/erosions in the small bowel mucosa on capsule endoscopy before and after taking the NSAIDs and Probiotics/Placebo | From enrollment to the end of treatment at 8 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Change from Baseline in Gastrointestinal Symptom Rating Scale (GSRS) Questionnaire Scores | Change from Baseline in Gastrointestinal Symptom Rating Scale Questionnaire Scores at 8 Weeks
|
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Jae Myung Park, MD | Contact | +82222586023 | parkjerry@catholic.ac.kr |
| Name | Affiliation | Role |
|---|---|---|
| Jae Myung Park, MD | The Catholic University of Korea | Study Chair |
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| ID | Term |
|---|---|
| D010003 | Osteoarthritis |
| ID | Term |
|---|---|
| D001168 | Arthritis |
| D007592 | Joint Diseases |
| D009140 | Musculoskeletal Diseases |
| D012216 | Rheumatic Diseases |
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| ID | Term |
|---|---|
| D019936 | Probiotics |
| ID | Term |
|---|---|
| D019587 | Dietary Supplements |
| D005502 | Food |
| D000066888 | Diet, Food, and Nutrition |
| D010829 | Physiological Phenomena |
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Probiotics group vs. Placebo group
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| Placebo capsule | Combination Product | Subjects will take a placebo capsule identical in shape and size to probiotics capsule three times a day for 8 weeks in combination with NSAIDs |
|
| From enrollment to the end of treatment at 8 weeks |
| Change From Baseline in Symptom Scores on the Western Ontario and McMaster Universities (WOMAC) Arthritis Index |
| From enrollment to the end of treatment at 8 weeks |
| Change From Baseline in Symptom Scores on the Knee Injury and Osteoarthritis Outcome Scores (KOOS) Questionnaire at 8 Weeks |
| From enrollment to the end of treatment at 8 weeks |
| Changes in the gut microbiome through Next Generation Sequencing |
| From enrollment to the end of treatment at 8 weeks |
| D019602 |
| Food and Beverages |