To evaluate the effectiveness and safety of tacrolimus eye drops (FK-506) in the treatment of Posner-Schlossman Syndrome. It is expected to collect 30 patients with PSS who are in the Ophthalmology Department of Peking University Third Hospital. The included PSS patients were divided into experimental group and control group using simple randomization method. Among them, the experimental group was treated with FK-506 twice a day, and the control group was treated with prednisolone acetate ophthalmic suspension 1% 4 times a day. For all PSS patients whose intraocular pressure is higher than 30mmHg, also add brinzolamide eye drops 3 times a day. Best corrected visual acuity, Goldmann intraocular pressure, anterior section photographs, corneal endothelial cells,corneal confocal microscope, Heidelberg retinal nerve analysis, Octopus visual field were examined on baseline and 1 week, 2 weeks, 3 weeks, 4 weeks after the treatment.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Twice a day
Four times a day
Peking University Third Hosipital
Beijing, Beijing Municipality, China
RECRUITINGSilt-lamp examination of the cornea
KP numbers after the treatment
Time frame: 1 week after the treatment
Silt-lamp examination of the cornea
KP numbers after the treatment
Time frame: 2 weeks after the treatment
Silt-lamp examination of the cornea
KP numbers after the treatment
Time frame: 3 weeks after the treatment
Silt-lamp examination of the cornea
KP numbers after the treatment
Time frame: 4 weeks after the treatment
Goldmann ophthalmotonometer examination of intra-ocular pressure
change of intra-ocular pressure
Time frame: 1 week after the treatment
Goldmann ophthalmotonometer examination of intra-ocular pressure
change of intra-ocular pressure
Time frame: 2 weeks after the treatment
Goldmann ophthalmotonometer examination of intra-ocular pressure
change of intra-ocular pressure
Time frame: 3 weeks after the treatment
Goldmann ophthalmotonometer examination of intra-ocular pressure
change of intra-ocular pressure
Time frame: 4 weeks after the treatment
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