Clinical Trials Directory

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UnknownNCT00744666

IntraVitreal Triamcinolone Acetonide: Preventing Raised Eye-pressure by Tracking Elevations After Topical Steroids

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
70 (estimated)
Sponsor
Hotel Dieu Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Intravitreal triamcinolone acetonide (IVTA) is a commonly employed treatment for various vitreoretinal disorders. However, approximately 23% to 50% of patients who receive IVTA develop ocular hypertension after the drug is injected into the eye. Similar to IVTA, topically administered corticosteroids eye drops result in ocular hypertension in approximately 33% of the population. It is unknown whether identifying patients who develop ocular hypertension from topical corticosteroids could be used to identify patients who are at risk for injectable IVTA. Therefore, the purpose of this study is to evaluate the efficacy of topical prednisolone 1% four times daily for one month as a screening test to reduce the incidence and severity of ocular hypertension after IVTA injection.

Conditions

Interventions

TypeNameDescription
DRUGPrednisolone 1% topical eye dropsPrednisolone 1% 1gtt qid to the eye requiring IVTA

Timeline

Start date
2008-09-01
Primary completion
2010-06-01
Completion
2010-07-01
First posted
2008-09-01
Last updated
2009-08-06

Locations

4 sites across 1 country: Canada

Source: ClinicalTrials.gov record NCT00744666. Inclusion in this directory is not an endorsement.