Pediatric Zylet Safety and Efficacy Study

PHASE4CompletedINTERVENTIONAL
Enrollment

108

Participants

Timeline

Start Date

November 30, 2006

Primary Completion Date

January 31, 2009

Study Completion Date

June 30, 2009

Conditions
ChalazionHordeolum
Interventions
DRUG

loteprednol etabonate/tobramycin opthalmic suspension

Topical ophthalmic drug: 0.5% loteprednol etabonate with 0.3% tobramycin 4 times a day (QID) days 1-7, 2 times a day (BID) days 8-14. Warm compresses were applied to affected eyes 2 times a day prior to application of study medication.

DRUG

vehicle

topical ophthalmic vehicle was applied 4 times a day (QID) days 1-7, 2 times a day (BID) days 8-14. Warm compresses were applied to affected eyes 2 times a day prior to application of study medication.

Trial Locations (1)

16501

Pediatric Ophthalmology of Erie, Erie

All Listed Sponsors
lead

Bausch & Lomb Incorporated

INDUSTRY

NCT00420628 - Pediatric Zylet Safety and Efficacy Study | Biotech Hunter | Biotech Hunter