This 12-week randomized, open-label study evaluates the efficacy and safety of Tacrolimus for Sjogren's syndrome patients with thrombocytopenia.
This study evaluates the efficacy and safety of Tacrolimus for the treatment of thrombocytopenia in Sjogren's syndrome patients.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
54
Oral hydroxychloroquine 200mg twice daily for 12weeks.
Oral Tacrolimus 1-2mg twice daily for 12 weeks.
Complete response rate
Complete response (platelet counts \> 100×10\^9/L) rates at week 12.
Time frame: week 12
Complete response rate
Complete response (platelet counts \> 100×10\^9/L) rates at week 4 and week 8.
Time frame: week 4 and week 8
ESSDAI improvement
Change from baseline in ESSDAI (EULAR Sjogren's Syndrome Disease Activity Index) score at week 12.
Time frame: week 12
ESSPRI improvement
Change from baseline in ESSPRI (EULAR Sjogren's Syndrome Patient Reported Index) score at week 12.
Time frame: week 12
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