Submitted for Publication: August 1, 2013; final revision received December 16, 2013; accepted December 19, 2013.
Published Online: April 24, 2014. doi:10.1001/jamaophthalmol.2014.292.
Study concept and design: Ray, Srinivasan, Glidden, Oldenburg, Zegans, McLeod, Lietman.
Acquisition, analysis, or interpretation of data: Ray, Srinivasan, Mascarenhas, Rajaraman, Ravindran, Glidden, Oldenburg, Sun, Zegans, Acharya, Lietman.
Drafting of the manuscript: Ray, Lietman.
Critical revision of the manuscript for important intellectual content: Ray, Srinivasan, Mascarenhas, Rajaraman, Ravindran, Glidden, Oldenburg, Sun, Zegans, McLeod, Acharya, Lietman.
Statistical analysis: Ray, Glidden, Oldenburg, Lietman.
Obtained funding: Lietman.
Administrative, technical, or material support: Ray, Srinivasan, Mascarenhas, Rajaraman, Ravindran, Oldenburg, Acharya.
Study supervision: Srinivasan, Zegans, Lietman.
Conflict of Interest Disclosures: None reported.
Funding/Support: This study was supported by grants U10 EY015114 (Dr Lietman) and K23 EY017897 (Dr Acharya) from the National Eye Institute, and a Research to Prevent Blindness Award (Dr Acharya). Alcon provided moxifloxacin (Vigamox) for the trial. The Department of Ophthalmology at the University of California, San Francisco, is supported by core grant EY02162 from the National Eye Institute.
Role of the Sponsors: The funding sources had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.