NCT06767917

A Post-Market Clinical Follow-Up on Safety and Performance of the Ophthalmic Viscoelastic Devices Eyefill SC and Eyefill MB

Safety and Performance of the Ophthalmic Viscoelastic Devices Eyefill SC and Eyefill MB - a Post-Market Clinical Follow-Up

• Status: Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 150 (estimated)
• Sponsor: Bausch & Lomb GmbH · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

Prospective, Non-comparative, Post Market Clinical Follow Up Study to demonstrate safety and performance of Eyefill® S.C. and Eyefill® M.B. as viscoelastic devices for cataract surgery

Conditions

• Cataract

Interventions

Type	Name	Description
DEVICE	Eyefill® S.C.	Used as viscoelastic devices during cataract surgery
DEVICE	Eyefill® M.B.	Used as viscoelastic devices during cataract surgery

Timeline

• Start date: 2024-11-26
• Primary completion: 2026-01-01
• Completion: 2026-01-01
• First posted: 2025-01-10
• Last updated: 2025-06-24

Locations

2 sites across 1 country: Spain