Pharmacokinetics Clinical Trial
Official title:
The Pharmacokinetics of Aqueous Dexamethasone and the Inflammatory Cytokine Response After Treatment With a Dexamethasone Intracanalicular Insert - The CYTODEX Study
Verified date | October 2022 |
Source | Bucci Laser Vision Institute |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The study is being done to measure the absorption of the DEXTENZA implant and inflammation concentration levels in the eye.
Status | Active, not recruiting |
Enrollment | 102 |
Est. completion date | January 2023 |
Est. primary completion date | October 31, 2021 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 55 Years and older |
Eligibility | Inclusion Criteria: - Male of female, aged 55 or older - Scheduled to undergo phacoemulsification with the intraocular lens (IOL) implantation for the treatment of cataract - Willing to comply with study instructions, agree to make study appointments, and complete the course of the study - Must sign an informed consent document indicating that they understand the purpose of and procedures required for the study and are willing to participate Exclusion Criteria: - Known allergy or contraindication to the test article or its components - Presence of any ocular abnormality or significant illness that, in the investigator's opinion, could affect the subject's health - History of any illness that could be expected to interfere with the study - Any condition that, in the opinion of the investigator, would compromise the well-being of the subject or study - May not be currently using topical or systemic steroids or NSAIDs during the course of the study or within 4 weeks prior to enrolling in the study other than Dextenza and Omidria - Subject has active corneal, conjunctival, or canalicular infections, including: - Epithelial herpes simplex keratitis (dendritic keratitis) - Vaccini - Varicella - Mycobacterial infections - Fungal diseases of the eye - Dacryocystitis |
Country | Name | City | State |
---|---|---|---|
United States | Bucci Laser Vision | Wilkes-Barre | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
Frank A. Bucci, Jr., M.D. |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pharmacokinetics in Aqueous Humor Samples | Concentration of dexamethasone in the aqueous humor will be determined by an independent laboratory using standardized high-pressure liquid chromatography and mass spectrometry assasys. Pharmacokinetic parameters determined from aqueous humor concentration will minimally include maximum concentration (Cmax). | Measured 1-3 days, 6-8 days, 13-15 days, 19-23 days, and 26-31 days after Dextenza insertion | |
Primary | Pharmacokinetics in Aqueous Humor Samples | Concentration of inflammatory cytokines (IL-1 beta, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12 (p70), IL-13, TNF alpha, and IFN gamma) in the aqueous humor will be determined by an independent laboratory using standardized high-pressure liquid chromatography and mass spectrometry assasys. Pharmacokinetic parameters determined from aqueous humor concentration will minimally include maximum concentration (Cmax). | Measured 1-3 days, 6-8 days, 13-15 days, 19-23 days, and 26-31 days after Dextenza insertion | |
Secondary | Correlation between dexamethasone levels and inflammatory cytokines | Test for statistically significant correlations between the aqueous concentrations of dexamethasone and inflammatory cytokines (IL-1 beta, IL-2, IL-4, IL-6, IL-8, IL-10, IL-12 (p70), IL-13, TNF alpha, and IFN gamma) over time | 1-3 days, 6-8 days, 13-15 days, 19-23, or 26-31 days after Dextenza insertion |
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