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Completed

NCT Number: NCT05740293

Post-approval Study of New Enrolment Patients Undergoing Bilateral Treatment With the VisuMax SMILE Procedure

The objective of the post-approval study (PAS) is to assess patient experience of visual symptoms 6 months after bilateral treatment with the VisuMax SMILE procedure as measured by a patient questionnaire.

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Key information

Age range

22 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Vold Vision, Fayetteville, Arkansas, United States

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About this study

This is a prospective, multicenter, single arm, open-label, observational study of newly enrolled patients undergoing bilateral treatment with the approved SMILE procedure for the reduction or elimination of myopia with astigmatism. Patients complete a self-administered patient questionnaire preoperatively and 6 months postoperatively. Each patient's preoperative status is serving as the control for postoperative endpoints.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Eligible for the approved VisuMax SMILE procedure according to the Professional Use Information, i.e.
  • Spherical refractive error (in minus cylinder format) from -1.00 D through -10.00 D;
  • Refraction spherical equivalent not greater in magnitude than 10.00 D;
  • Minimum age of 22 years;
  • Documentation of stable manifest refraction over the past year as demonstrated by a change in sphere and cylinder of ≤ 0.50 D in magnitude.
  • Good candidate for SMILE based on the surgeon's assessment of medical and ophthalmic health, cognitive function, and physical and social limitations
  • Intended bilateral SMILE treatment for the correction of myopia with astigmatism (-0.75 to -3.00 D)
  • Both eyes targeted for the full distance manifest spherocylindrical refraction
  • Fluent English in speaking and reading
  • Willingness and ability to return for 6-month postoperative examination
  • Signed informed consent

Exclusion criteria

  • Presence of any of the contraindications of the approved SMILE procedure for the reduction or elimination of myopia with astigmatism, i.e.
  • a residual stromal bed thickness that is less than 250 microns from the corneal endothelium;
  • abnormal corneal topographic findings, e.g. keratoconus, pellucid marginal degeneration;
  • ophthalmoscopic signs of progressive or unstable myopia or keratoconus (or keratoconus suspect);
  • irregular or unstable (distorted/not clear) corneal mires on central keratometry images;
  • severe dry eye;
  • active eye infection or inflammation;
  • recent herpes eye infection or problems resulting from past infection;
  • active autoimmune disease or connective tissue disease;
  • uncontrolled diabetes;
  • uncontrolled glaucoma.
  • Previous treatment with any form of refractive surgery

Treatment and study plan

VisuMax SMILE procedure for the reduction or elimination of myopia with astigmatism

Procedure

Bilateral treatment with the approved VisuMax SMILE procedure for the reduction or elimination of myopia with astigmatism.

Primary outcomes

  1. Development of clinically relevant visual symptoms via questionnaire responses

    Time frame: 6 months

    • Proportion of subjects that developed "very" or "extremely" bothersome visual symptoms from preoperative (with optical correction) to 6 months postoperatively (without optical correction)
    • Proportion of subjects that developed difficulty performing daily activities (2 highest categories) due to visual symptoms from preoperative (with optical correction) to 6 months postoperatively (without optical correction)

Secondary outcomes

  1. Resolution of clinically relevant visual symptoms via questionnaire responses

    Time frame: 6 months

    • Proportion of subjects that showed resolution of "very" or "extremely" bothersome visual symptoms from preoperative (with optical correction) to 6 months postoperatively (without optical correction)
    • Proportion of subjects that showed resolution of difficulty performing daily activities (2 highest categories) due to visual symptoms from preoperative (with optical correction) to 6 months postoperatively (without optical correction)
  2. Development and resolution of all visual symptoms via questionnaire responses

    Time frame: 6 months

    • Proportion of subjects that developed visual symptoms from preoperative (with optical correction) to 6 months postoperatively (without optical correction)
    • Proportion of subjects that showed resolution of visual symptoms from preoperative (with optical correction) to 6 months postoperatively (without optical correction)
  3. Dry eye via questionnaire responses

    Time frame: 6 months

    • Proportion of subjects that developed dry eye symptoms as compared to their preoperative status (OSDI score from normal at preoperative to abnormal at 6 months; categorized according to Miller et al. 2010)
    • Proportion of subjects that showed resolution of dry eye symptoms as compared to their preoperative status (OSDI score from abnormal at preoperative to normal at 6 months; categorized according to Miller et al. 2010)
  4. Satisfaction via questionnaire responses

    Time frame: 6 months

    • Proportion of patients satisfied with their vision after the SMILE procedure (who responded "completely satisfied", "very satisfied", or "somewhat satisfied" to the corresponding questionnaire item)
    • Proportion of patients satisfied with the SMILE procedure (based on a score ≥ 40 in the corresponding 8-item questionnaire domain)

Sponsors and collaborators

Lead sponsor

Carl Zeiss Meditec, Inc.

Industry

Registry information

Important dates

Study start
2022
Primary completion
2024
Study completion
2025
First posted
Feb 23, 2023
Registry last updated
Aug 29, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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