Dry Eye Clinical Trial - Evaluation of Safety & Tolerability of Ocular

Clinical Trial 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. ;

Study Design

See also
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NCT number	NCT05573360
Study type	Interventional
Source	Alcon Research
Contact
Status	Completed
Phase	N/A
Start date	December 16, 2022
Completion date	May 31, 2023

Evaluation of Safety and Tolerability of Ocular Lubricants

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms