Intraocular Lens Associated Postoperative Inflammation
Conditions
Brief summary
To compare the relative effectiveness of the Imprimis Dropless™ (TriMoxiVanc) intraocular solution with the Less Drops™ topical formulation of PredMoxiKeterolac (given for the first week post op) followed by PredKeterolac (given for weeks 2 to 4 after surgery). The hypothesis is that the dropless regimen will be non-inferior to the less drops regimen in terms of post-operative IOP changes, post-operative healing, and visual quality.
Detailed description
Modern cataract surgery has become a relatively short out-patient procedure with small incisions and short post-operative recovery time. Surgery can be influenced by surgical technique and experience. Prophylactic pharmaceutical regimens are designed to control post-operative pain and to reduce the potential for inflammation (i.e. macular edema, CME) and infection (i.e. endophthalmitis). The most serious potential infection related to cataract surgery is endophthalmitis. Endophthalmitis is a result of microorganisms entering the eye, either during the surgical procedure or before surgical incisions have healed completely. The risk of infection can be reduced in several ways. Pre-operatively, reducing the bacteria on the cornea and ocular adnexa can be helpful. During surgery, appropriate technique can reduce the potential for ingress. Post-operatively, prophylactic antibiotics can eliminate organisms once they have entered the eye. Topical drops, intracameral antibiotics and subconjunctival injections are typical options in current use, usually selected on the basis of spectrum of coverage, cost, efficacy and/or expected side effects. With regard to inflammation, one of the most common post-operative responses is cystoid macular edema (CME). Steroids and non-steroidal anti-inflammatory drugs (NSAIDs) appear effective in reducing the incidence of CME, with NSAIDs posing a lower risk for IOP spikes and showing greater efficacy some studies. While there is documented evidence of the utility of prophylactic post-operative treatment for pain and infection, patient compliance remains a significant concern. The regimen is often complex, with multiple drops several times per day. Inability to instill the drops, forgetfulness and a lack of appreciation for the importance of compliance can all be contributing factors. There are several new options to try to address the potential issues related to poor patient compliance. One is referred to as dropless cataract surgery, which involves injection of a multi-drug compound into the eye at time of cataract surgery; one such compound includes triamcinolone acetonide, moxifloxacin hydrochloride and vancomycin (TriMoxiVanc). Another alternative is to reduce the burden of the pharmaceutical regimen using a compounded topical medication; this is termed less drops cataract surgery. An option in this regard is a topical formulation of prednisolone acetate, moxifloxacin hydrochloride and ketorolac tromethamine (PredMoxiKetorolac), given for one week post-operatively followed by a topical formulation of prednisolone acetate and ketorolac tromethamine (PredKeterolac) given for weeks 2 to 4 after surgery. The purpose of this study is to evaluate the differences in performance between the dropless and less-drops pharmaceutical regimens after cataract surgery.
Interventions
Tri-Moxi-Vanc transzonular intravitreal injection
Pred-Moxi-Ketorolac and Pred-Ketorolac topical instillation qd postoperatively
Sponsors
Study design
Eligibility
Inclusion criteria
* Ocular criteria must be met in both eyes. * Subject is undergoing bilateral cataract extraction or refractive lens exchange with intraocular lens implantation. * Gender: Males and Females. * Age: 21 or older. * Willing and able to provide written informed consent for participation in the study. * Willing and able to comply with scheduled visits and other study procedures. * Willing and able to administer eye drops and record the times the drops were instilled. * Scheduled to undergo standard cataract surgery or refractive lens exchange with topical anesthesia in both eyes within 6-15 days of each other. * Potential postoperative best-corrected visual acuity of 20/30 or better.
Exclusion criteria
* If any of the following
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The Change in Intraocular Pressure (IOP) From Baseline | To end of study (1 month postop) | Based on Goldmann tonometry |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in Corneal Thickness | To end of study (1 month postop) | Based on corneal pachymetry |
| Slit Lamp (Cornea Exam) | To end of study (1 month postop) | — |
Other
| Measure | Time frame | Description |
|---|---|---|
| The Change From Baseline in Visual Symptoms | To end of study (1 month postop) | visual symptom scale |
| Subject Reporting no Eye Pain | To end of study (1 month postop) | 0( on the eye pain/discomfort scale) |
| The Change From Baseline in Macular Thickness Measurements | To end of study (1 month postop) | based on optical coherence tomography (OCT) measurement |
| The Change From Baseline in Central Corneal Thickness Measurements | To end of study (1 month postop) | corneal pachymetry |
| Change From Baseline Eye Pain/Discomfort | To end of study (1 month postop) | eye pain/discomfort scale |
| The Proportion of Subjects Reporting no Visual Symptoms (0 ) | To end of study (1 month postop) | visual symptom scale |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Imprimis Dropless TriMoxiVanc 0.2cc intravitreal one time
Imprimis Dropless: Tri-Moxi-Vanc transzonular intravitreal injection | 0 |
| Imprimis Less Drops Pred Moxi, 1 drop tid for 1 week then, PredKeterolac bid for 2-4 weeks.
Imprimis Less Drops: Pred-Moxi-Ketorolac and Pred-Ketorolac topical instillation qd postoperatively | 0 |
| Total | 0 |
Baseline characteristics
| Characteristic | — |
|---|---|
| Region of Enrollment United States | — participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 0 | 0 / 0 |
| other Total, other adverse events | 0 / 0 | 0 / 0 |
| serious Total, serious adverse events | 0 / 0 | 0 / 0 |
Outcome results
The Change in Intraocular Pressure (IOP) From Baseline
Based on Goldmann tonometry
Time frame: To end of study (1 month postop)
Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report
Change in Corneal Thickness
Based on corneal pachymetry
Time frame: To end of study (1 month postop)
Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report
Slit Lamp (Cornea Exam)
Time frame: To end of study (1 month postop)
Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report
Change From Baseline Eye Pain/Discomfort
eye pain/discomfort scale
Time frame: To end of study (1 month postop)
Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report
Subject Reporting no Eye Pain
0( on the eye pain/discomfort scale)
Time frame: To end of study (1 month postop)
Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report
The Change From Baseline in Central Corneal Thickness Measurements
corneal pachymetry
Time frame: To end of study (1 month postop)
Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report
The Change From Baseline in Macular Thickness Measurements
based on optical coherence tomography (OCT) measurement
Time frame: To end of study (1 month postop)
Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report
The Change From Baseline in Visual Symptoms
visual symptom scale
Time frame: To end of study (1 month postop)
Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report
The Proportion of Subjects Reporting no Visual Symptoms (0 )
visual symptom scale
Time frame: To end of study (1 month postop)
Population: Study data has been lost to natural disaster (Hurricane Micheal), therefore there is no study data that is available to report