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Optimal time after instillation of cyclopentolate 1% for maximum cycloplegia in Thai children

Optimal time after instillation of cyclopentolate 1% for maximum cycloplegia in Thai children

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20140219001
Enrollment
43
Registered
2014-02-19
Start date
2013-10-30
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Pateints that needs to be cycle&#45

Interventions

None listed

Sponsors

Ratchadapiseksompotch Research Fund
Lead Sponsor
1.) Ratchadapiseksompotch Research Fund
Collaborator

Eligibility

Sex/Gender
All
Age
5 Years to 10 Years

Inclusion criteria

Inclusion criteria: Patients 5-10 yrs. of age that need to be cyclo-refraction

Exclusion criteria

Exclusion criteria: 1. Anterior segment disorder that interfere the auto-refraction (e.g corneal scar, lens opacity) 2. History of corneal or cataract surgery and glaucoma 3. History of ophthalmic disease other than refractive error and/or strabismus 4. History of allergy to cyclopentolate 1% 5. Insufficient cooperation interfere with instillation of eye-drop or auto-refraction

Design outcomes

Primary

MeasureTime frame
To determine the optimal time of maximum cycloplegic effect after instillation of cyclopentolate 1% 90 mins To determine the optimal time of maximum cycloplegic effect after instillation of cyclopentolate 1%

Secondary

MeasureTime frame
To find the relationship between pupillary dilatation and cycloplegic effect 90 mins To find the relationship between pupillary dilatation and cycloplegic effect,To find the data of side effect of cyclopentolate 1% in Thai children 90 mins To find the data of side effect of cyclopentolate 1% in Thai children

Countries

Thailand

Contacts

Public ContactSittikorn Laojareonwanit

Department of ophthalmology, Faculty of medicine, Chulalongkorn University

Sittikorn.lao@gmail.com080-4915550

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026