Actively Recruiting
Probiotics in Adults With Rheumatoid Arthritis
Led by Ancilia Biosciences · Updated on 2025-12-31
50
Participants Needed
1
Research Sites
15 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical study is to collect data on the effect of probiotic administration on clinical outcomes in rheumatoid arthritis patients. Participants will: * Have a 6-week daily administration of a probiotic * Collect fecal samples every other day during the first 3 weeks of the study and twice weekly over the last 3 weeks * Visit the clinic at Baseline, Week 3 and Week 6 for checkup and testing
CONDITIONS
Official Title
Probiotics in Adults With Rheumatoid Arthritis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Able to give written informed consent.
- 18 years or older.
- Clinical diagnosis of rheumatoid arthritis for more than 6 months.
- On stable rheumatoid arthritis treatment for at least 3 months and expected to remain stable during the study.
- Willing to take the study probiotic daily for the entire study period.
You will not qualify if you...
- Pregnant, breastfeeding, or planning pregnancy during the study.
- Of childbearing potential but not using effective contraception as specified.
- History of drug or alcohol abuse.
- Food allergies or issues preventing intake of study products including milk and soy allergies.
- Significant acute or chronic health conditions that could affect study participation or results, including certain autoimmune diseases, other inflammatory joint diseases, gastrointestinal diseases or surgeries, kidney failure, and liver cirrhosis.
- Recent use of antibiotics within 8 weeks.
- Recent use of probiotics supplements within 4 weeks.
- Recent consumption of yoghurts containing probiotics within 2 weeks.
- Considered unlikely to comply with study visits or requirements.
- Currently participating in other clinical studies or insufficient time elapsed since prior experimental study participation.
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Atlantia Clinical Trials
Chicago, Illinois, United States, 60611
Actively Recruiting
Research Team
S
Stacey Boetto, DNP, FNP-C
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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