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Clinical Trial Summary

Prospective data on the visual acuity response in children treated by patching concurrently treated with caffeine and estimate the magnitude of effect that might be seen in a randomized trial (if no improvement in acuity is seen, this would be sufficient evidence to decide not to conduct a randomized, double blind trial).

Collect prospective data on the tolerability of caffeine in two dosages as an adjuvant treatment for amblyopia and provide limited data on its safety.

Evaluate the potential for a dietary intervention to enhance the acceptance and tolerability of patching on the child and family.

Demonstrate recruitment potential of subjects to participate in a dietary intervention study.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02594358
Study type Interventional
Source Johns Hopkins University
Contact
Status Withdrawn
Phase Phase 1/Phase 2
Start date October 2014
Completion date December 2018

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