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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04667507
Other study ID # IIT-CYTODEX
Secondary ID
Status Active, not recruiting
Phase Phase 4
First received
Last updated
Start date January 1, 2021
Est. completion date January 2023

Study information

Verified date October 2022
Source Bucci Laser Vision Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study is being done to measure the absorption of the DEXTENZA implant and inflammation concentration levels in the eye.


Recruitment information / eligibility

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

Study Design


Intervention

Drug:
Dexamethasone Ophthalmic implant
Dexamethasone ophthalmic insert 0.4 mg for intracanalicular use

Locations

Country Name City State
United States Bucci Laser Vision Wilkes-Barre Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Frank A. Bucci, Jr., M.D.

Country where clinical trial is conducted

United States, 

Outcome

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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