The purpose of this study was to determine the safety and retention times of two different lengths (10 mm and 20 mm) of the MINI MONOKA canicular stent when inserted in the eye for up to three months in subjects with or without dry eye.

This study consisted of 6 visits conducted over a period of 3 months. At Visit 1 (Day 0), the canalicular stent was inserted. If the stent insertion failed, the subject was rescheduled for insertion at the Day 2 visit. If the stent insertion was not successfully completed by the end of the Day 2 visit, the subject was discontinued from the study. Any subject who had the stent inserted but lost the stent (noticed or unnoticed) after the Day 2 Visit was considered to have completed the study.

Inclusion Criteria:

• Sign Informed Consent.
• With or without dry eye.
• Willing to discontinue contact lenses during the study.
• Other protocol-defined inclusion criteria may apply.

Exclusion Criteria:

• Chronic, recurrent, or severe inflammatory eye disease.
• Ocular trauma within the past 6 months.
• Ocular hypertension or glaucoma.
• History of punctal plug/canalicular stent insertion.
• Other protocol-defined exclusion criteria may apply.

This reporting group includes all randomized participants for whom stent insertion was successfully completed (57).

Adverse events were collected for the duration of the study (3 months, 26 days)

The safety population includes all subjects randomized into the study for whom an attempt to insert a canalicular stent occurred.