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Hypothetical clinical trial of safety improvement by Triamsinolone in vitreous surgery

Hypothetical clinical trial of safety improvement by Triamsinolone in vitreous surgery - Safty of Triamsinolone in vitreous surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000007500
Enrollment
500
Registered
2013-09-12
Start date
2010-12-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

the patients who perform vitreous surgery

Interventions

Triamcinolone acetonide

Sponsors

Department of Ophthalmology, Yamaguchi University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: the patient who will perform vitreous surgery

Exclusion criteria

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.

Design outcomes

Primary

MeasureTime frame
complications in vitreous surgery

Secondary

MeasureTime frame
visual acuity, ocular pressure, fundus examination, postoerative complications

Countries

Japan

Contacts

Public ContactKazuhiro Kimura

Yamaguchi University Graduate School of Medicine Ophthalmology

k.kimura@yamaguchi-u.ac.jp+81-836-222278

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026