Combining structure and function to evaluate glaucomatous progression: implications for the design of clinical trials
dc.contributor.author | Lisboa, Renato [UNIFESP] | |
dc.contributor.author | Weinreb, Robert N. | |
dc.contributor.author | Medeiros, Felipe A. | |
dc.contributor.institution | Univ Calif San Diego | |
dc.contributor.institution | Universidade Federal de São Paulo (UNIFESP) | |
dc.date.accessioned | 2016-01-24T14:31:13Z | |
dc.date.available | 2016-01-24T14:31:13Z | |
dc.date.issued | 2013-02-01 | |
dc.description.abstract | The selection of a suitable method for assessment of glaucomatous progression and estimation of rates of change is an essential component of the design of clinical trials investigating neuroprotective therapies for the disease. Due to the limitations of currently available tests, approaches combining structural and functional tests are essential in order to provide reliable detection of endpoints. This could also potentially enable shorter clinical trials with relatively smaller sample size requirements. A recent approach for estimating rates of retinal ganglion cell loss using a combination of structural and functional tests has been shown to perform better than isolated parameters from conventional tests for diagnosing, staging and detecting glaucoma progression and may prove useful as an outcome measure in clinical trials of the disease. | en |
dc.description.affiliation | Univ Calif San Diego, Hamilton Glaucoma Ctr, San Diego, CA 92103 USA | |
dc.description.affiliation | Univ Calif San Diego, Dept Ophthalmol, San Diego, CA 92103 USA | |
dc.description.affiliation | Universidade Federal de São Paulo, Dept Ophthalmol, São Paulo, Brazil | |
dc.description.affiliationUnifesp | Universidade Federal de São Paulo, Dept Ophthalmol, São Paulo, Brazil | |
dc.description.source | Web of Science | |
dc.description.sponsorship | NIH/NEI | |
dc.description.sponsorship | Research to Prevent Blindness (New York, NY) | |
dc.description.sponsorship | Carl-Zeiss Meditec, Inc | |
dc.description.sponsorshipID | NIH/NEI: EY021818 (FAM) | |
dc.format.extent | 115-122 | |
dc.identifier | http://dx.doi.org/10.1016/j.coph.2012.10.010 | |
dc.identifier.citation | Current Opinion in Pharmacology. Oxford: Elsevier B.V., v. 13, n. 1, p. 115-122, 2013. | |
dc.identifier.doi | 10.1016/j.coph.2012.10.010 | |
dc.identifier.issn | 1471-4892 | |
dc.identifier.uri | http://repositorio.unifesp.br/handle/11600/35930 | |
dc.identifier.wos | WOS:000314329300018 | |
dc.language.iso | eng | |
dc.publisher | Elsevier B.V. | |
dc.relation.ispartof | Current Opinion in Pharmacology | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.rights.license | http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy | |
dc.title | Combining structure and function to evaluate glaucomatous progression: implications for the design of clinical trials | en |
dc.type | info:eu-repo/semantics/article |