Analysis of Influencing Factors of High-Order Aberrations of SMILE With Lenticule Retained

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-45
SponsorSecond Affiliated Hospital of Nanchang University

About this trial

Analysis of Influencing Factors of High-Order Aberrations of SMILE with Lenticule Retained

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 18 years, gender unrestricted;

Equivalent spherical refraction ≤ -10.0D, corrected distance visual acuity ≥ 1.0, myopia stable for ≥ 2 years, and no contact lens wear for at least 2 weeks;

The patient voluntarily participates in this study, signs the informed consent form, and agrees to follow up according to the study plan;

Predicted postoperative residual corneal stromal thickness ≥ 280 micrometers.

Disqualifiers

Subclinical keratoconus, keratoconus, moderate to severe corneal opacities or scars, and other ocular conditions;

Diabetes, keloid-prone constitution, autoimmune and connective tissue diseases, etc.;

Severe mental disorders such as generalized anxiety disorder, panic disorder, depression, schizophrenia, and bipolar disorder; inability to cooperate with physicians;

Refusal to participate in the study.

Trial population

Each subject must have complete surgical video recordings and medical records.

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

33 Participants
are grouped into 2 trial groups
Group A: lenticule retained group
Group B: Non-lenticule retained group

Trial outcomes

Primary outcomes

1

Δ Higher-order Aberration

Preoperative and postoperative Higher-order aberration difference obtained from wavefront aberrations map of corneal topography in Pentacam measurement.

Time frame
Day 90

Secondary outcomes

Other outcomes

Sponsors and contacts

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