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Optical Quality of the Cornea in Orthokeratology

NCT06775509 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 23

Last updated 2025-01-15

No results posted yet for this study

Summary

Analyzing Optical Quality After the Use of Overnight Orthokeratology (Ortho-K)

Conditions

  • Myopia (Disorder)
  • Astigmatism

Interventions

DEVICE

Ortho-K

Utilization of Ortho-K Contact Lenses for The Treatment of Myopia

Sponsors & Collaborators

  • Institut Investigacio Sanitaria Pere Virgili

    lead OTHER

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
12 Years
Max Age
21 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-11-01
Primary Completion
2025-07-01
Completion
2025-12-31
FDA Device
Yes

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06775509 on ClinicalTrials.gov