NCT05573360

Evaluation of Safety and Tolerability of Ocular Lubricants

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 41 (actual)
• Sponsor: Alcon Research · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

The purpose of this study is to evaluate the safety profile of test formulations for an artificial tear product versus a comparator product.

Detailed description

Subjects will be randomized to one of five different treatment sequences. Subjects will attend 6 scheduled visits with an expected individual duration of participation of 11 to 42 days. This study will be conducted in Australia.

Conditions

• Dry Eye

Interventions

Type	Name	Description
OTHER	NGF5-A test formulation	One drop of investigational product instilled on the eye
OTHER	NGF4-B test formulation	One drop of investigational product instilled on the eye
OTHER	NGF6-B test formulation	One drop of investigational product instilled on the eye
OTHER	NGF6-E test formulation	One drop of investigational product instilled on the eye
OTHER	Systane eye drop	One drop of commercial product instilled on the eye

Timeline

• Start date: 2022-12-16
• Primary completion: 2023-05-31
• Completion: 2023-05-31
• First posted: 2022-10-10
• Last updated: 2023-07-06

Locations

2 sites across 1 country: Australia