Midland Eye
Solihull, B91 2AW, United Kingdom
NCT Number: NCT04730336
Pilot study where effect of standard Tixel treatment as used for periorbital wrinkles would be assessed on Dry Eye Disease symptoms and signs
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Solihull, B91 2AW, United Kingdom
Safety Assessment will be asses via AE/SAE reporting and Impact Assessment of the effect of treatment on dry eye symptoms and signs through multiple test indicate Dry Eye
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Peri-Orbital fractional treatment on the Eye-Lid to assess the effect on Dry Eye symptoms
Other names: Fractional
Time frame: 18 Weeks
Non-Invasive Break Up Time
Time frame: 18 Weeks
Total 12 questions will be asked, ranked between 0-100. 0 being no dry eye symptoms and 100 severe dry eye symptoms.
Time frame: 18 Weeks
Any safety related event during the study will be recorded and analyzed
Time frame: 18 Weeks
Topography with K readings
Time frame: 18 Weeks
Multiple Slit Lamp tests
Time frame: 18 Weeks
Assessment of the frequency and severity of dry eye symptoms. scored 0 to 28; 0 being no dry eye symptoms and 28 severe dry eye symptoms.
Time frame: 18 Weeks
Lid margin profile
Time frame: 18 Weeks
ocular tear biomarkers
Time frame: 18 Weeks
Corneal staining fluorescein and conjunctival/lid margin staining lissamine green
Aston University
Other
Assessment of the Impact of Tixel Treatment of Periorbital Wrinkles on Dry Eye Symptoms and Signs in Patients With Dry Eye
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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