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The efficacy of puls methylprednisolone in the treatment of patients with ocular involvement in Behcet's disease

Phase 4
Conditions
ocular involvement in behcet's disease.
Behcet's disease
Registration Number
IRCT201011235235N1
Lead Sponsor
Rheumatology Research Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
34
Inclusion Criteria

Diagnosed Behcet's disease according to international criteria, New or relapse of retinal vasculitis who received any cytotoxic or glucocorticoid since 2 months ago, or new or relapse of severe posterior uveitis who are candidate for cyclophosphamide and azathioprine according to their physician
Exclusion criteria: not Signing the informed consent, Visual acuity lower than 1/10 by Snellen chart, presence of infectious diseases such as TB, presence of diabetes mellitus, hypertension, heart disease, liver disease, renal disease, or edema, presence of other glucocorticoid consumption contraindications

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Ocular IBDDAM INDEX. Timepoint: Before and 2 months after treatment. Method of measurement: ophthalmologist record.;Visual acuity. Timepoint: Before intervention and then every 2 months for 6 months. Method of measurement: ophthalmologist record.
Secondary Outcome Measures
NameTimeMethod
Inflammation in retina. Timepoint: Before and two months after intervention. Method of measurement: ophthalmologist record.
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