Last updated: November 23, 2023
Sponsor: He Eye Hospital
Overall Status: Active - Recruiting
Phase
N/A
Condition
Myopia
Treatment
0.9% sodium chloride
0.01% atropine
Clinical Study ID
NCT06034366
atropine2023
Ages 6-12 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Age 6 to 12 years
- Subjects and their guardians agreed to participate in this study
- Best-corrected visual acuity (BCVA) 0.1 (log minimum angle of resolution, LogMAR) orbetter.
- Initial NITM (spherical equivalent) ≤ -0.25 D
- Cycloplegic refractions ≥ -1.0 D and astigmatism ≤ 2.5 D in both eyes.
- Anisometropia in both eyes ≤ 1.5 D
Exclusion
Exclusion Criteria:
- Children with existing systemic diseases including asthma, collagen disease, immunesystem disorders, prostate hypertrophy, spastic paralysis, Down's syndrome, severecardiac, pulmonary, hepatic, and renal dysfunction.
- Patients with glaucoma or high intraocular pressure, ocular inflammatory diseases,strabismus, amblyopia, corneal diseases, diseases of lens, retinal and opticneuropathy
- Regular use of medications that may affect the efficacy of 0.01% atropine, includinghairy fruit rutabaga eye drops, tropicamide eye drops, anticholinergic drugs such aspirenzepine and tropicamide, and cholinergic drugs such as carbachol and hairy fruitrutabaga.
- Previous experiences with myopia control therapy.
- A history of allergies to atropine.
- Patients were deemed inappropriate for trial participation by the lead investigator.
Study Design
Total Participants: 150
Treatment Group(s): 2
Primary Treatment: 0.9% sodium chloride
Phase:
Study Start date:
October 01, 2023
Estimated Completion Date:
May 31, 2025
Study Description
Connect with a study center
He Eye Hospital
Shenyang, Liaoning 110034
ChinaActive - Recruiting
He Eye Specialist Hospital
Shenyang, 110034
ChinaActive - Recruiting

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