Clinical Trials Directory

Trials / Completed

CompletedNCT00992355

Tobramycin-Dexamethasone Versus Tobramycin-Dexamethasone Plus Ketorolac After Phacoemulsification Surgery

Tobramycin 0.3% - Dexamethasone 0.1% Versus Tobramycin 0.3% - Dexamethasone 0.1% Plus Ketorolac Tromethamine 0.5% After Phacoemulsification Surgery. A Randomized Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
97 (actual)
Sponsor
Veroia General Hospital · Academic / Other
Sex
All
Age
55 Years – 95 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGTobramycin 0.3% - Dexamethasone 0.1%
DRUGTobramycin 0.3% - Dexamethasone 0.1% plus Ketorolac tromethamine 0.5%

Timeline

Start date
2009-01-01
Primary completion
2009-03-01
Completion
2009-04-01
First posted
2009-10-09
Last updated
2009-10-09

Locations

1 site across 1 country: Greece

Source: ClinicalTrials.gov record NCT00992355. Inclusion in this directory is not an endorsement.