Patient Satisfaction With Contoura Vision Topography-Guided LASIK

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-05-21

Study Completion Date

2023-11-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

To evaluate patient reported outcomes associated with quality of vision before and after treatment with Contoura Vision Topography-Guided LASIK.

Related Clinical Trials

Explore similar clinical trials based on study characteristics and research focus.

Patient Reported Satisfaction With Contoura LASIK Utilizing the Phorcides Analytic Software

NCT05848817

Myopia

COMPLETED

Clinical and Refractive Outcomes After Contoura® Refractive Surgery Planned Using Phorcides Surgery Planning Software

NCT04495829

Refractive Errors

COMPLETED

Contralateral Study of Topography Guided LASIK Versus Small Incision Lenticule Extraction

NCT05611294

Myopia Astigmatism

ACTIVE_NOT_RECRUITING NA

LASIK Using Contoura With Phorcides vs. iDesign

NCT07128316

Myopia Astigmatism

ACTIVE_NOT_RECRUITING NA

CONTOURA vs WFO Ablation PRK & LASIK

NCT05037370

Refractive Surgery

RECRUITING NA

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Myopia Astigmatism

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Study Group

Contoura Vision LASIK using Phorcides Analytic Software

Group Type EXPERIMENTAL

Contoura Vision LASIK

Intervention Type PROCEDURE

Topography-Guided LASIK using Phorcides Analytic Software

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Contoura Vision LASIK

Topography-Guided LASIK using Phorcides Analytic Software

Intervention Type PROCEDURE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

Eligibility criteria: The study enrollment will include all willing patients with: pre-operative BCVA 20/20 for each eye individually, myopic refractive error up to -8.00 diopters, refractive astigmatism that ranges from 0 to 3 diopters, maximum spherical equivalent of -9.00 diopters, the designated age requirements, and only patients that have signed the informed consent document.

Exclusion Criteria

Exclusion criteria: Patients are excluded that are not willing to participate in a research trial, are unable to cooperate well enough to safely perform the procedure, fail to meet inclusion criteria, have ocular disease (including but not limited to keratoconus, macular degeneration, glaucoma, corneal dystrophy, dry eye syndrome and corneal scarring), and patients that have had previous ocular surgery. Any patients with known allergies to the post-operative medications or preservatives in the medications will also be excluded.

Minimum Eligible Age

21 Years

Maximum Eligible Age

35 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes