Status:
COMPLETED
DEXTENZA Compared to Topical Steroid Therapy Prior to Cataract Surgery in Patients Who Receive Premium Intraocular Lenses
Lead Sponsor:
Prism Vision Group
Conditions:
Cataract
Eligibility:
All Genders
18+ years
Phase:
PHASE4
Brief Summary
The investigators seek to assess the effect of pre-operative and continued post-operative corticosteroid use on pain, patient preference, visual outcomes, and change in objective quantifiable biologic...
Eligibility Criteria
Inclusion
- • Age 18 or greater with plans to undergo bilateral clear cornea cataract surgery with phacoemulsification and implantation of a premium posterior chamber IOL
- Schirmer's test score (anesthetized) ≥ 5 mm at Screening in either eye.
- TBUT ≤ 7 seconds at Screening or Baseline in either eye.
- All subjects must provide signed written consent prior to participation in any study-related procedures. Able to comply with study requirements and visit schedule.
Exclusion
- revious corneal surgery or pathology
- Active or history of chronic or recurrent inflammatory eye disease in either eye
- Ocular pain in either eye
- Proliferative diabetic retinopathy in either eye
- Significant macular pathology detected on macular optical coherence tomography evaluation at the screening visit in either eye
- Laser or incisional ocular surgery during the study period and 6 months prior in either eye
- Prescription and OTC ophthalmic mast cell stabilizers and antihistamines within 21 days prior to Screening and throughout the study period (systemic mast cell stabilizers are allowed, and systemic antihistamines are permitted)
- Chronic daily use (defined as \> 7 consecutive days at the recommended dosing frequency) of systemic narcotics for any chronic pain syndrome (eg, fibromyalgia, rheumatoid arthritis, etc.) during the study period.
- Ophthalmic artificial tear drop use within 2 hours prior to any study visit. Any OTC artificial tear (preserved or unpreserved) should be continued at the same frequency and with no change in drop brand.
- Use of any topical prescription ophthalmic medications (including cyclosporine \[Restasis®, Cequa®\] or topical lifitegrast \[Xiidra®\], steroids, nonsteroidal anti- inflammatory drugs \[NSAIDs\], anti-glaucoma medications within 7 days or during study period
- Participation in any drug or device clinical investigation within 30 days prior to entry into this study and/or during the period of study participation.
- Corticosteroids (intranasal, inhaled, topical dermatological, and perianal steroids) within 30 days prior to entry in the study are not permitted
- Pregnant or breast-feeding women, women who wish to become pregnant during the length of study participation, or women of child-bearing potential.
- Use of systemic NSAID greater than 375 mg per day.
- Glaucoma or is on medications to treat glaucoma.
- Ocular Hypertension, defined as IOP of \>21 mmHg, is on medications to treat hypertension or has a history of IOP spikes in either eye including steroid-related IOP increases.
- Presence of nasolacrimal duct obstruction or history of cauterization of the Punctum.
- Active epiphora or clinically significant dry eye syndrome.
- Know allergy or sensitivity to the investigational product or its components.
- The Investigator determines that the subject should not be included for reasons not already specified (e.g, systemic or other ocular disease/abnormality) if the health of the subject or the validity of the study outcomes may be compromised by the subject's enrollment.
Key Trial Info
Start Date :
October 1 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 12 2022
Estimated Enrollment :
13 Patients enrolled
Trial Details
Trial ID
NCT04479748
Start Date
October 1 2020
End Date
December 12 2022
Last Update
June 22 2023
Active Locations (1)
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1
Eye Associates of Vineland
Vineland, New Jersey, United States, 08361