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Effect of symbiotic supplementation in rheumatoid arthritis

Not Applicable
Conditions
Rheumatoid Arthritis.
Rheumatoid arthritis with rheumatoid factor
Registration Number
IRCT20121216011763N37
Lead Sponsor
the University of medical sciences Esfahan
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
200
Inclusion Criteria

Rheumatoid arthritis patients (based on ACR criteria)
At least 3 months after the diagnosis of RA.
At least 4 swollen joints which were in a stable status for at least 1 month, on MTX and prednisolone

Exclusion Criteria

Drug reaction and hypersensitivity
patient dissatisfaction
consumption of probiotic oral or medical in the last 2 weeks
IBD
intestinal perforation
creatinine clearance by using the CKD-EPI equation of less than 40 mL/min per 1.73 m2
aspartate and alanine aminotransferase levels greater than twice the upper limit of normal
active or recent hepatitis or cirrhosis
plan for surgery in the next 3 months
thyroid disorders
Cushing's disease or syndrome
malignant tumors,
inadequately controlled diabetes mellitus or arterial hypertension
serious infections,
serious cardiac or respiratory diseases, leukopenia or thrombocytopenia,
inadequate contraception, pregnancy or a plan for it in the next 3 months, breastfeeding,
osteoporosis,
use of cytotoxic or immunosuppressive drugs for 3 months before inclusion,
current or past substance abuse (including tobacco) or alcohol use greater than 2 U/d
and psychological illnesses or intellectual disorders that would preclude adherence to the study protocol

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Severity of disease activity. Timepoint: At the beginning of the study and 3 months after starting the drug. Method of measurement: Physical examination for the number of tender joint (T1) and swellen j (S1) and blood tests (ESR, CRP, ALT, Cr), calculate DAS28 according to ESR, Tender Joint, Sowllen joint and VAS dat.
Secondary Outcome Measures
NameTimeMethod
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