Evaluating Crosslinked Hyaluronate Canalicular Gel for the Treatment of DED in Patients Undergoing Cataract Surgery

Recruiting now · Not applicable

Conditions studied: Dry Eye Disease (DED)

In brief

To review how patients report using a hyaluronate crosslinked canalicular gel placed before cataract surgery

Key facts

Study ID

NCT07155057

Run by

Vance Thompson Vision

People needed

60

Starts

2025-09-03

Expected to finish

2026-12-01

Last updated by the study team

2025-09-29

Who can join

Age: 22 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• 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

You may not qualify if…

• History of punctal cautery
• Lacrimal anatomy (e.g., nasolacrimal duct obstruction) that per investigator suggests that the patient would not be a good candidate for lacrimal occlusion or patients for whom lacrimal occlusion would increase risk

Where it is running

• Vance Thompson Vision Clinic, Prof. LLC — Sioux Falls, South Dakota, United States (enrolling)

Full record on ClinicalTrials.gov

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