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Direct Comparison of TG and WFO LASIK

Contralateral Comparison of Togoguided LASIK and Wavefront-optimized LASIK

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04919291
Enrollment
21
Registered
2021-06-09
Start date
2019-09-26
Completion date
2020-06-30
Last updated
2021-06-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Contrast Sensitivity, Keratomileusis, Laser In Situ

Brief summary

To compare the efficacy to different profiles, direct head-to-head studies had been conducted. In one previous review study revealed that TG LASIK provided patient with better uncorrected visual acuity (UCVA) than WFO LASIK and WFG LASIK. In recent previous contralateral eye studies also showed that TG LASIK induced less postoperative higher-order aberration than WFO LASIK. However, these studies included only low-to-moderate myopia patients, for patients with high myopia (spherical equivalent \> 6D), the effect of TG LASIK comparing with WFO LASIK had not been reported before. The aim of our study is to analyze and compare the visual performance of TG LASIK and WFO LASIK in high myopia and low-to-moderate myopia patients, , particularly UCVA, corrected distance visual acuity (CDVA), contrast sensitivity (CS), and wavefront aberration.

Interventions

DEVICETopoguided LASIK

Topoguided ablation profile on dominant eye

Wavefront optimized ablation profile on non-dominant eye

Sponsors

Taipei Nobel Eye Clinic
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* age between 20 and 50 years old * CDVA of both eyes could reach 0.1 logarithm of the minimum angle of resolution (logMAR) * stable refractive errors of myopia and astigmatism

Exclusion criteria

* cataract * corneal opacities or irregularities * dry eye (Schirmer's test I ≤ 5mm) * amblyopia * coexisting ocular pathologies * glaucoma * non-dilating pupil * history of intraocular surgery, laser therapy, or retinopathy * optic nerve or macular diseases * estimated postoperative cornea residual stromal thickness less than 250 μm * pregnancy or under lactation * uncontrolled diabetic mellitus or systemic immune disease * refusal or unable to maintain follow-up

Design outcomes

Primary

MeasureTime frameDescription
Visual acuity3 months after surgeryuncorrected visual acuity and corrected distance visual acuity
Corneal wavefront analysis3-months postoperative visithorizontal coma aberration (Z 3,1), spherical aberration (Z 4,0), and trefoil aberration
Contrast sensitivity3-months postoperative visit4 spatial frequencies: 3, 6, 12, and 18 cycles per degree (cpd).
Quality of vision questionnaire3-months postoperative visitA 11-item questionnaire, item scores range from 0 to 10 and higher item scores in questionnaire indicated more difficulty in achieving specific visual tasks

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026