Skip to main content
OpenTrials
Completed

NCT Number: NCT03244670

The Incidence and Progression of Myopia: Cohort Study

A cohort study on incidence and progression of myopia in a group of medical students

Completed

Looking for future studies?

Notify Me

Key information

Age range

17 year–23 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Zhongshan Ophthalmic Center

Guangzhou, Guangdong, 510060, China

About this study

A prospective cohort study to investigate the refractive error development, progression and their risk factors in young adult population comprises a group of medical students in China for two years

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Volunteer subject, , willing to follow the protocol and able to read, comprehend and sign the informed consent form,
  • Age between 17 and 23 years

Exclusion criteria

  • Vulnerability of the subject,
  • Participation in another study which might have an influence on vision or interfere with study assessments,
  • Aphakic or pseudophakic (intraocular lens)
  • Participants who are wearing ortho-K lenses, or undergone any kind of myopia control treatments or undergone refractive surgery.
  • Any current or evolving pathology manifested in the eye or the appendages which might have an influence on vision, or interfere with study assessments (e.g. AMD, glaucoma…),
  • Any previous ocular surgery which might have an influence on vision or interfere with study assessments (e.g. iridectomy, refractive surgery…),
  • Any untreated and/or uncontrolled systemic condition which might have an influence on vision, or interfere with study assessments (e.g. uncontrolled diabetes, uncontrolled high blood pressure…),
  • Any medical treatment or medication which might have an influence on vision or interfere with study assessments (e.g. antidepressants, drugs with atropinic effects…),

Treatment and study plan

Observation study only, no specific intervention

Other

Observation study only, no specific intervention

Primary outcomes

  1. refraction

    Time frame: Change from baseline for two years

    The participants will be measured for their refractive error by optometrist, and observe the rate of progression of myopia

Sponsors and collaborators

Lead sponsor

Sun Yat-sen University

Other

Collaborators

  • Essilor International

Registry information

Official study title

A Cohort Study on Incidence and Progression of Myopia in a Group of Medical Students

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Aug 9, 2017
Registry last updated
Sep 20, 2019

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.

Published trials that share one or more normalized conditions with this study.