Evaluating Crosslinked Hyaluronate Canalicular Gel for the Treatment of DED in Patients Undergoing Cataract Surgery
Vance Thompson Vision · NCT07155057
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 22+ · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Not applicable
- Target enrollment
- 60
- US sites recruiting
- 1
- Study start
- September 3, 2025
- Record last updated
- September 29, 2025
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
To review how patients report using a hyaluronate crosslinked canalicular gel placed before cataract surgery
Being studied: Cross-Linked Hyaluronate Gel Prefilled Syringe 30 MG/3ML
Conditions: Dry Eye Disease (DED)
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- 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
Exclusion Criteria
- 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
Recruiting US locations
Vance Thompson Vision Clinic, Prof. LLC
Sioux Falls, SD 57105
Site contact: Tiffany R Facile · tiffany.facile@vancethompsonvision.com
Study contacts (from the official record)
- Tiffany Facile · 605-371-7075 · tiffany.facile@vancethompsonvision.com
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