Evaluation of Reflex Tear Production
- Conditions
- Dry Eye Disease
- Registration Number
- NCT06565624
- Lead Sponsor
- Alcon Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not yet recruiting
- Sex
- All
- Target Recruitment
- 80
Key Inclusion Criteria:<br><br> - Within the last 12 months, have a previous history of dry eye disease, either<br> clinician diagnosed or patient reported.<br><br> - Within the last 6 months, have used, or desired to use artificial tears for dry eye<br> symptoms.<br><br> - Corrected Visual Acuity (Snellen) 20/200 or better in both eyes.<br><br> - Good general and ocular health, as determined by the investigator using medical<br> history, ophthalmic examination and history.<br><br> - Able, as assessed by the investigator, and willing to follow study instructions.<br><br> - Other protocol-specified inclusion criteria may apply.<br><br>Key Exclusion Criteria:<br><br> - Current evidence of any clinically significant ophthalmic disease other than dry eye<br> (for example, glaucoma or macular degeneration).<br><br> - Use of artificial tears within 2 hours of the Study Visit.<br><br> - History of ocular surgery within 1 year of the Study Visit.<br><br> - Use of contact lenses in either eye within 7 days of the Study Visit.<br><br> - Use of lid hygiene (all forms of lid care) or heat masks within 7 days of the Study<br> Visit.<br><br> - Use of any topical ocular anti-inflammatory medications, any topical ocular<br> corticosteroid, or any non-steroidal-anti-inflammatory agents within 30 days of the<br> Study Visit.<br><br> - Other protocol-specified exclusion criteria may apply.
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change from baseline in TMH immediately following stimulation
- Secondary Outcome Measures
Name Time Method