Skip to content

Nearwork-induced transient myopia (NITM) in ametropia among young adults

Nearwork-induced transient myopia (NITM) in ametropia among young adults

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OON-17013899
Enrollment
Unknown
Registered
2017-12-13
Start date
2018-01-01
Completion date
Unknown
Last updated
2017-12-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Integration, translation and development on Ophthalmic technology

Interventions

myopia group:Close reading
emmetropia group:Close reading
hyperopia group:Close reading

Sponsors

Beijing Institute of Ophthalmology, Beijing Tongren Hospital, Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 26 Years

Inclusion criteria

Inclusion criteria: (1) Sign informed consent; (2) After mydriasis optometry : myopia group:in the eyes of any spherical equivalent of -0.5D to -6.00D; emmetropia group: in the eyes of any spherical equivalent of -0.5D to +0.5D; hyperopia group: in the eyes of any spherical equivalent of +0.5D to +2.0D; (3) The best corrected visual acuity in both eyes was greater than or equal to 1; (4) At any eye in the eyes, the smooth astigmatism is less than 1.5D, and the reverse astigmatism is less than 0.75 D; (5) The Anisometropia of the eyes is less than 1.00D; (6) Normal intraocular pressure, without strabismus, amblyopia, or any other pathological changes of the eyeball; (7) Diseases that have no influence on visual development or refractive development, such as diabetes and fibrous tissue lesions.

Exclusion criteria

Exclusion criteria: (1) Eye examination can not be carried out; (2) At any eye, the best corrected visual acuity was less than 1; (3) According to the judgment of the researcher, the person who can not understand or cooperate with the research program; (4) Participating in other clinical trials or participating in other clinical trials within the first 30 days of the study; (5) Unable to participate in this study voluntarily or not with high enthusiasm.

Design outcomes

Primary

MeasureTime frame
initial near work-induced transient myopia;decay time;

Countries

China

Contacts

Public ContactWang Ningli

Beijing Institute of Ophthalmology, Beijing Tongren Hospital, Capital Medical University

wningli@vip.163.com+86 13511026669

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026