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Clinical Trials/ISRCTN12292232
ISRCTN12292232
Completed
未知

Randomised trial of a personalised dosing strategy versus a standardised dosing strategy for childhood amblyopia

City University London (UK)0 sites120 target enrollmentDecember 17, 2013
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ConditionsTopic: Eye, Generic Health Relevance and Cross Cutting ThemesSubtopic: Eye (all Subtopics), Generic Health Relevance (all Subtopics)Disease: Ophthalmology, PaediatricsEye DiseasesAmblyopia ex anopsia

Overview

Phase
未知
Intervention
Not specified
Conditions
Topic: Eye, Generic Health Relevance and Cross Cutting Themes
Sponsor
City University London (UK)
Enrollment
120
Status
Completed
Last Updated
5 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

2015 protocol in: http://www.ncbi.nlm.nih.gov/pubmed/25906974

Registry
who.int
Start Date
December 17, 2013
End Date
March 1, 2015
Last Updated
5 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
City University London (UK)

Eligibility Criteria

Inclusion Criteria

  • •1\. The trial will recruit subjects with amblyopia associated with:
  • •1\.1\. Strabismus
  • •1\.2\. Anisometropia
  • •1\.3\. A combination of anisometropia and strabismus
  • •2\. Children aged between 3 and 8 years with visual acuity of 0\.2 logMAR or lower in the worst eye and an inter\-ocular difference of at least 0\.2 log units with the presence of anisometropia and/or strabismus and no other ocular pathology including amblyopia associated with form deprivation or previous occlusion treatment history will be eligible for recruitment.
  • •3\. Target Gender: Male \& Female

Exclusion Criteria

  • •1\. Those with other ocular pathology
  • •2\. Those with form deprivation amblyopia as this is a minority group and often is linked with other ocular pathology
  • •3\. Previous history of treatment for amblyopia
  • •4\. Those with learning difficulties and therefore cannot perform an accurate visual acuity test on every occasion tested

Outcomes

Primary Outcomes

Not specified

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