A Prospective, Single-Arm Study Evaluating Crosslinked Hyaluronate Canalicular Gel for the Treatment of Dry Eye Disease in Patients Undergoing Refractive Cataract Surgery
Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
To review how patients report using a hyaluronate crosslinked canalicular gel placed before cataract surgery
Eligibility
Participation Requirements
Sex: All
Minimum Age: 22
Healthy Volunteers: t
View:
• Be willing and able to understand and sign the informed consent form (ICF)
• Men or non-pregnant women age 22 or older
• Clear intraocular media other than cataract
• Diagnosis of dry eye disease (OSDI score ≥ 13)
• Non-invasive Tear break up time ≤ 10 seconds in at least one eye
• Willing and able to comply with all study related visits and procedures
• In the opinion of the investigator, patients who are appropriate for advanced technology lens implants
Locations
United States
South Dakota
Vance Thompson Vision Clinic, Prof. LLC
RECRUITING
Sioux Falls
Contact Information
Primary
Tiffany Facile
tiffany.facile@vancethompsonvision.com
605-371-7075
Time Frame
Start Date: 2025-09-03
Estimated Completion Date: 2026-12
Participants
Target number of participants: 60
Treatments
Other: Study Participants
Patients will receive bilateral lacrimal occlusion of crosslinked hyaluronate canalicular gel pre-operatively
Related Therapeutic Areas
Sponsors
Leads: Vance Thompson Vision