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Hypothetical clinical trial of safety improvement by Triamsinolone in vitreous surgery

Not Applicable
Recruiting
Conditions
the patients who perform vitreous surgery
Registration Number
JPRN-UMIN000007500
Lead Sponsor
Department of Ophthalmology, Yamaguchi University Graduate School of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
500
Inclusion Criteria

Not provided

Exclusion Criteria

1)The contraindications item in a triamcinolone acetonide package leaflet (1)This agent ingredient hypersensitivity 2)The contraindications item at the time of whole body medication of a steroid hormone agent (1)The patient of the infection in which effective antibacterial medicine does not exist, and the mycosis of the whole body, (2) The patient of digestive ulcer, (3) The patient of a mental disease, (4) The patient of a tubercular disease, (5) The patient of simple herpetic keratitis, (6)The patient of after cataract, (7)The patient of glaucoma, (8)The patient of hypertension, (9)The patient with electrolyte abnormalities, (10)The patient of thromboses, (11)The patient with the operative wound of the recent internal organs, and (12) acute myocardial infarction, (13)The patient judged that medication of a steroid hormone agent is not desirable for the caused eye disease of a patient and others, or systemic illness 3)The patient who this research responsibility (assignment) doctor accepted was unsuitable as a subject 4)The participation in other clinical study is unquestioned.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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