Medications Effect on Lenstar Measurements
NCT02780063 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50
Last updated 2019-01-25
Summary
Prior to cataract surgery the lens must be calculated to appropriately fit a patient for the intraocular lens implant. Lenstar is an optical biometer that calculates the axial length, keratometry, lens thickness, pupillometry, and anterior chamber depth. Dilation drops are routinely used in eye exams in addition to pre-cataract surgery. The dilation drops include Tropicamide 1%, and Phenylephrine 2.5%. The Tropicamide achieves the dilation of the pupil which causes an anterior rotation of the ciliary body, which may affect the Lenstar measurements. This study is to determine if dilating medications affect the lens power prediction for emmetropia by the Lenstar biometer. Prior to dilation, Lenstar biometry will be performed on each eye. Patients will receive dilation medication and after waiting 20 minutes Lenstar biometry will be performed on each eye. Dilation and measurement with Lenstar will be done as standard of care. Measurements and calculations from before and after will be compared.
Conditions
- Cataract
Interventions
- OTHER
-
Lenstar Biometer
uses optical principles (laser interferometry) to measure axial length, measuring distance from the corneal apex to the retinal RPE. In addition to axial length, it also measures corneal thickness, anterior chamber depth, lens thickness, radii of curvature of flat and steep meridian, axis of flat meridian, white to white distance, and pupil diameter.
Sponsors & Collaborators
- lead OTHER
Principal Investigators
-
Ann Ostrovsky, MD · NYU Langone Health
Study Design
- Allocation
- NA
- Purpose
- SCREENING
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 50 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2015-09-18
- Primary Completion
- 2018-07-24
- Completion
- 2018-07-24
Countries
- United States
Study Locations
More Related Trials
-
Comparison of Corticosteroid Dosing Regimens After Endothelial Keratoplasty
NCT01853696 ·Status: COMPLETED ·Phase: PHASE4
-
DEXTENZA Compared to Topical Steroid Therapy Prior to Cataract Surgery in Patients Who Receive Premium Intraocular Lenses
NCT04479748 ·Status: COMPLETED ·Phase: PHASE4
-
Ketorolac vs. Steroid in the Prevention of CME
NCT00348244 ·Status: COMPLETED ·Phase: PHASE4
-
Ocular Penetration of Topical Tacrolimus Eye Drops
NCT02794610 ·Status: UNKNOWN ·Phase: NA
-
Assessing eFficacy and Safety of DEXTENZA 0.4 mg inseRt, Following Cataract Surgery
NCT05626478 ·Status: COMPLETED ·Phase: PHASE4
-
Aqueous Concentrations and PGE2 Inhibition of Ketorolac 0.4% vs. Bromfenac 0.09% in Cataract Patients
NCT00347503 ·Status: COMPLETED ·Phase: PHASE4
-
A Comparison of 0.5% Loteprednol Etabonate Versus 1% Prednisolone Acetate Following Cataract Surgery
NCT01384266 ·Status: COMPLETED
-
Evaluation of a Protocol of Pupil Dilation Before Laser-assisted Cataract Surgery
NCT03375996 ·Status: COMPLETED
-
Ketorolac Plus Tobramycin/Dexamethasone Versus Tobramycin/Dexamethasone After Uneventful Phacoemulsification Surgery
NCT01103401 ·Status: COMPLETED ·Phase: NA
-
Comparison Mydriasis by Mydrane With Topical Drop Application
NCT04880928 ·Status: COMPLETED ·Phase: PHASE4
-
Eye Drop Application Monitor, Pilot Study
NCT02639845 ·Status: UNKNOWN
-
Loteprednol Etabonate Versus Vehicle for the Treatment of Inflammation and Pain Following Cataract Surgery
NCT01010633 ·Status: COMPLETED ·Phase: PHASE3
-
Bioavailability of Bimatoprost Ophthalmic Solution in Human Aqueous.
NCT00355446 ·Status: COMPLETED ·Phase: PHASE4
-
The Effect of Voltaren-ophtha 0.1% Eye Drops on INR Levels (International Normalized Ratio) in Patients Taking Warfarin
NCT02782338 ·Status: UNKNOWN
-
The Effect of Ophthalmic Solutions on Contact Lenses Used After Surgery for Congenital Cataract Investigated in Vivo
NCT03125785 ·Status: UNKNOWN
-
Intraocular Steroid After Cataract Surgery Study
NCT00478764 ·Status: COMPLETED ·Phase: NA
-
Loteprednol Etabonate Ophthalmic Ointment vs. Vehicle in the Treatment of Inflammation Following Cataract Surgery
NCT00645671 ·Status: COMPLETED ·Phase: PHASE3
-
The Role of Loteprednol in Reducing Post-Intravitreal Injection Related Pain
NCT05542381 ·Status: COMPLETED ·Phase: NA
-
In Clinic Optometrist Insertion of Dextenza Prior to Cataract Surgery
NCT05023304 ·Status: COMPLETED ·Phase: PHASE4
-
Evaluation of Loteprednol Etabonate Versus Vehicle for the Treatment of Inflammation and Pain Following Cataract Surgery
NCT01060072 ·Status: COMPLETED ·Phase: PHASE3
-
Lidocaine Usage for Pupil Dilatation (Mydriasis)
NCT01170130 ·Status: COMPLETED ·Phase: NA
-
The Use of Sublingual Melatonin Premedication in Geriatric Cataract Surgery
NCT07036367 ·Status: RECRUITING ·Phase: PHASE4
-
Aqueous Concentrations and PGE2 Inhibition of Ketorolac 0.4% vs. Bromfenac 0.09% in Cataract Patients: Trough Drug Effects
NCT00469690 ·Status: COMPLETED ·Phase: PHASE4
-
Chloroprocaine 3% Gel Eye Drop as Topical Anestheticsin Phacoemulsification.
NCT04685538 ·Status: COMPLETED ·Phase: PHASE3
-
A Bioequivalence Study to Compare the Pharmacokinetics (PK) Of Marketed Product TobraDex® To An Experimental Ophthalmic Sterile Ointment Containing Tobramycin And Dexamethasone In Aqueous Humor In Patients Undergoing Indicated Cataract Surgery
NCT02734459 ·Status: COMPLETED ·Phase: PHASE3