Investigating the Safety and Effect of Overnight Orthokeratology and Its Influencing Factors

NCT04910451 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 400

Last updated 2021-06-02

No results posted yet for this study

Summary

To investigate the Safety and Effect of Overnight Orthokeratology and Its Influencing Factors in China

Conditions

  • Myopia

Interventions

OTHER

No Intervention

Sponsors & Collaborators

  • Second Affiliated Hospital, School of Medicine, Zhejiang University

    lead OTHER

Principal Investigators

  • Zhiwen Bian, doctor · 2nd Affiliated Hospital, School of Medicine, Zhejiang University, China

Eligibility

Min Age
8 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-07-01
Primary Completion
2022-07-01
Completion
2022-07-01

Countries

  • China

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 NCT04910451 on ClinicalTrials.gov