Efficacy and Safety Assessment of Intracameral Injection of T2380 in Cataract Surgery

• Status: Completed
• Trial end date: 2013-05-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to determine the efficacy and safety assessment of T2380 for mydriasis and anaesthesia in phacoemulsification cataract surgery versus reference group (topical mydriatics and anaesthetic) 2X246 patients.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Laboratoires Thea
• Treatments: Anesthetics; Mydriatics; Tetracaine; Tropicamide

Criteria

Inclusion Criteria:

• Signed and dated informed consent

• Male or female aged from 40 to 88 years old

• Scheduled to undergo unilateral cataract surgery

Exclusion criteria:

• Combined surgery

• Previous intraocular surgery