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Clinical Trial Summary

This randomized controlled trial compares two regimens of topical therapy:

- tobramycin 0.3% - dexamethasone 0.1% (TobraDex®, Alcon), one drop four times/day

- combination of tobramycin 0.3% - dexamethasone 0.1% (TobraDex®, Alcon), one drop four times/day, plus Ketorolac tromethamine 0.5% (Acular®, Allergan), one drop three times/day. The topical treatment is administered for 28 days after phacoemulsification.

Patients are independently assessed by two ophthalmologists. On day 28, patients are evaluated for

- corneal edema

- conjunctival redness

- anterior chamber reaction. Moreover, the cases necessitating continuation of treatment are compared in the two groups on day 28 and 42.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00992355
Study type Interventional
Source Veroia General Hospital
Contact
Status Completed
Phase N/A
Start date January 2009
Completion date April 2009

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