The Eye Care Institute
Louisville, Kentucky, 40206, United States
NCT Number: NCT04022382
A study which participants with mild to moderate dry eye disease will have a punctum of one eye injected with 0.1ml Restylane Defyne and the other eye injected with 0.2ml Restylane Defyne. Participants will be evaluated over four visits.
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Notify Me21 year–80 year
All sexes
Interventional
Not applicable
Louisville, Kentucky, 40206, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Restylane is a gel of hyaluronic acid generated by Streptococcus species of bacteria, chemically crosslinked with BDDE, stabilized and suspended in phosphate buffered saline at pH=7 and concentration of 20 mg/mL.
Time frame: 30 days
Maximum length of tears absorbed on test strips recorded.
Time frame: 30 Days
Participants answer 12 question questionnaire. Scores from section I,II, and III.
Time frame: 30 Days
1.0mg sodium fluorescein strips on lower eye lids for one minute. 5 corneal regions graded using cobalt filter to maximized view of fluorescence.
Time frame: 30 days
Time frame: 30 days
Performed by Keratograph 5M per manufacturer's directions.
Time frame: 30 days
Performed by Keratograph 5M per manufacturer's directions.
John C Meyer, MD
Other
A Single-Arm, Single-Center, Randomized, Single-Masked Study to Evaluate Restylane-Defyne for Punctal Occlusion in Participants With Mild to Moderate Dry Eye Disease
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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