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Showing 1–4 of 4 matching trials from the live ClinicalTrials.gov search.
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Filters: Intervention: Limbal Relaxing Incision (LRI) Clear all
Completed Phase 1 Interventional Accepts healthy volunteers

Clinical Evaluation of TrueVision System: LRI and Capsulorhexis Templates

NCT01123343
View directory record Official record
Conditions
Subjects Undergoing Cataract Surgery and Insertion of IOL
Interventions
TrueVision 3D Visualization and Guidance System for MicroSurgery
Device
Lead sponsor
TrueVision Systems, Inc
Industry
Eligibility
18 Years and older
Enrollment
35 participants
Healthy volunteers
Accepts healthy volunteers
Timeline
2010
U.S. locations
1
States / cities
Eugene, Oregon
Source: ClinicalTrials.gov public record
Updated Jun 28, 2015 · Synced Sep 20, 2026, 3:37 PM EDT
Completed Not applicable Interventional Accepts healthy volunteers Results available

Femtosecond Laser-assisted Arcuate Incisions Versus Manual Arcuate Incisions Outcomes

NCT04126174
View directory record Official record
Conditions
Cataract
Interventions
femtosecond laser system arcuate corneal incision, Manual LRI
Device · Other
Lead sponsor
Gainesville Eye Associates
Other
Eligibility
40 Years and older
Enrollment
41 participants
Healthy volunteers
Accepts healthy volunteers
Timeline
2019 – 2021
U.S. locations
1
States / cities
Gainesville, Georgia
Source: ClinicalTrials.gov public record
Updated Sep 4, 2021 · Synced Sep 20, 2026, 3:37 PM EDT
Withdrawn Phase 4 Interventional

Comparison of Corneal Aberrations and Visual Outcomes in AcrySof IQ Toric Patients Versus Limbal Relaxing Incision (LRI) Patients

NCT00929747
View directory record Official record
Conditions
Cataracts
Interventions
Toric, Limbal Relaxing Incision
Device · Procedure
Lead sponsor
Alcon Research
Industry
Eligibility
18 Years to 70 Years
Healthy volunteers
Healthy volunteers not accepted
Timeline
2009
U.S. locations
1
States / cities
Fort Worth, Texas
Source: ClinicalTrials.gov public record
Updated Apr 11, 2012 · Synced Sep 20, 2026, 3:37 PM EDT
Completed Not applicable Interventional

A Comparison of Corneal Aberrations in Subjects With Contralateral AcrySof IQ Toric Intraocular Lens (IOL) and AcrySof IQ IOL With Limbal Relaxing Incision (LRI)

NCT01045733
View directory record Official record
Conditions
Cataract, Astigmatism
Interventions
AcrySof IQ Toric IOL, AcrySof IQ Aspheric IOL, Limbal Relaxing Incision (LRI)
Device · Procedure
Lead sponsor
Alcon Research
Industry
Eligibility
21 Years and older
Enrollment
70 participants
Healthy volunteers
Healthy volunteers not accepted
Timeline
2009 – 2011
U.S. locations
1
States / cities
Fort Worth, Texas
Source: ClinicalTrials.gov public record
Updated Nov 28, 2012 · Synced Sep 20, 2026, 3:37 PM EDT