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Accommodation response during low-dose atrophine (0.01%) in adolescents with mild myopia

Accommodation response during low-dose atrophine (0.01%) in adolescents with mild myopia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000034981
Enrollment
Unknown
Registered
2020-07-26
Start date
2020-07-20
Completion date
Unknown
Last updated
2020-07-27

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

Conditions

myopia

Interventions

Regulated normal group:Order atropine
Dysregulation group:Order atropine

Sponsors

Inner Mongolia Chaoju Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 15 Years

Inclusion criteria

Inclusion criteria: 1. Aged 6-15 years old; 2. The range of diopter (equivalent spherical lens) is between -0.50D~-3.00D; Progression in the past year is less than or equal to -3.00 diopters (D), and astigmatism is less than or equal to -2.50 D; 3. The best glasses corrected visual acuity (BSCVA) is 20/25 or higher; 4. Have not worn an orthokeratology lens; 5. Patients who are unwilling to wear frame glasses and adopt other correction or control methods, and are willing to accept experiments.

Exclusion criteria

Exclusion criteria: 1. Past cataracts, glaucoma, trauma and other eye diseases; 2. Diabetes; 3. The intraocular pressure is higher than 21mmHg; 4. Received atropine for mydriasis within three months; 5. Known atropine allergy history; 6. Have taken other methods to correct or control myopia.

Design outcomes

Primary

MeasureTime frame
UCVA;BCVA;Corneal thickness;intraocular pressure;Eye axis length;Flipper;AMP;BCC;

Secondary

MeasureTime frame
NRA;PRA;AC/A;

Countries

China

Contacts

Public ContactLi Huixia

40 Train Station Street West, New City District, Hohhot, Inner Mongolia Autonomous Region, China

1057600878@qq.com+86 13304710678

Outcome results

None listed

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