Autoimmune uveitis is one kind of non-infectious, sight-threatening, relapsing and severe ocular disease. Approximately 20%-25% autoimmune uveitis patients suffer from the dilemma of blindness for the chronic and persistent inflammatory state in the eyes, which results in continuous destroy in the structure of the eyes and gradually leads to irreversible damage on visual function. However, it shows limiting efficacy of current treatment including glucocorticoids, immunosuppressant and biologics for chronic autoimmune uveitis. Minocycline has been regarded to have anti-apoptosis and immunemodulatory function for decades and it has been illustrated to be beneficial in several neuro-degenerative and neuro-inflammatory diseases. This trial aims to investigate the efficacy and safety of minocycline for chronic autoimmune uveitis with retinal degenerative changes.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
minocycline capsule 100mg per day orally
Zhongshan Ophthalmic Center
Guangzhou, Guangdong, China
RECRUITINGChange of macular sensitivity
Change of macular sensitivity measured by MAIA
Time frame: At 6 and 12 months
Change of BCVA
Change of BCVA measured by ETDRS
Time frame: At 6 and 12 months
Change of Visual field
Change of Visual field measured by HVF 30-2 visual field testing
Time frame: At 6 and 12 months
Changes in Implicit Time and Amplitude of Photopic and Scotopic Responses
Changes in Implicit Time and Amplitude of Photopic and Scotopic Responses measured by Electroretinogram (ERG) Testing
Time frame: At 6 and 12 months
Change of macular vessel
Change of macular vessel measured by OCTA
Time frame: At 6 and 12 months
Change of Contrast Sensitivity
Change of Contrast Sensitivity measured by F.A.C.T
Time frame: At 6 and 12 months
Change of Color Visual
Change of Color Visual measured by FM100
Time frame: At 6 and 12 months
Change of QoL questionaire
Change of QoL measured by VFI-25
Time frame: At 6 and 12 months
Number of ocular and non-ocular adverse events Number of ocular and non-ocular adverse events Number of ocular and non-ocular adverse events Number of ocular and non-ocular adverse events Number of Ocular and Non-ocular Adverse Events
Time frame: At 6 and 12 months
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