Clinical Performance of Atypical Contact Lens Powers on Subjects With Astigmatism [clinicaltrials:NCT00697190]

Bio2RDF uri

Clinical Performance of Atypical Contact Lens Powers on Subjects With Astigmatism [clinicaltrials:NCT00697190]

Clinical Study [clinicaltrials_vocabulary:Clinical-Study]

clinicaltrials resource [clinicaltrials_vocabulary:Resource]

http://bio2rdf.org/clinicaltrials:NCT00697190

Bio2RDF identifier

NCT00697190

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Bio2RDF namespace

clinicaltrials

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Bio2RDF uri

http://bio2rdf.org/clinicaltrials:NCT00697190

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brief summary [clinicaltrials_vocabulary:brief-summary]

This study will evaluat ...... ses manufactured by Vistakon.

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brief title [clinicaltrials_vocabulary:brief-title]

Clinical Performance of Atypical Contact Lens Powers on Subjects With Astigmatism

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clinical result [clinicaltrials_vocabulary:clinical-result]

clinical results for clinicaltrials:NCT00697190 [clinicaltrials_resource:11694a3eabe529f92cff06e0ee343822]

clinicaltrials_vocabulary:primary outcome [clinicaltrials_vocabulary:clinicaltrials_vocabulary:primary-outcome]

Assessment of Conjunctival Hyperemia in Subjects That Are High Myopes (Have a High Degree of Nearsightedness) after 6 hours of wear [clinicaltrials_resource:1c93343262176310fbcada7bff311e60]

Assessment of Conjunctival Hyperemia in Subjects That Are High Myopes (Have a High Degree of Nearsightedness) after 6 hours of wear [clinicaltrials_resource:20516b4e76e8bd1488d04c98ee90bd87]

Assessment of Conjunctival Hyperemia in Subjects That Are High Myopes (Have a High Degree of Nearsightedness) after 6 hours of wear [clinicaltrials_resource:2e36a3306979ff4e32f7652c42e66a7c]

Assessment of Conjunctival Hyperemia in Subjects That Are High Myopes (Have a High Degree of Nearsightedness) after 6 hours of wear [clinicaltrials_resource:304193fe147e2ab5759dc860a6aa2dbf]

Assessment of Conjunctival Hyperemia in Subjects That Are High Myopes (Have a High Degree of Nearsightedness) after 6 hours of wear [clinicaltrials_resource:30f341067e481d006877d54b8b47cdbe]

Assessment of Conjunctival Hyperemia in Subjects That Are High Myopes (Have a High Degree of Nearsightedness) after 6 hours of wear [clinicaltrials_resource:3e24f0ba864ebba8351c67b5fa2ead60]

Assessment of Conjunctival Hyperemia in Subjects That Are High Myopes (Have a High Degree of Nearsightedness) after 6 hours of wear [clinicaltrials_resource:42f8fa80a1a0e71f6f6541e41914ebd2]

Assessment of Conjunctival Hyperemia in Subjects That Are High Myopes (Have a High Degree of Nearsightedness) after 6 hours of wear [clinicaltrials_resource:5a52b9796eb1d473fa9b90f88ae5606e]

Assessment of Conjunctival Hyperemia in Subjects That Are High Myopes (Have a High Degree of Nearsightedness) after 6 hours of wear [clinicaltrials_resource:5f35d86681c25a9aefb43571163daa0d]

Assessment of Conjunctival Hyperemia in Subjects That Are High Myopes (Have a High Degree of Nearsightedness) after 6 hours of wear [clinicaltrials_resource:688bf34977fa343366a97a933a33db8f]

completion date [clinicaltrials_vocabulary:completion-date]

2008-09-01T00:00:00Z

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condition [clinicaltrials_vocabulary:condition]

Astigmatism [clinicaltrials_resource:a137d033324766f64e5df746cab2c137]

condition browse [clinicaltrials_vocabulary:condition-browse]

Astigmatism [clinicaltrials_resource:a137d033324766f64e5df746cab2c137]

condition mesh [clinicaltrials_vocabulary:condition-mesh]

Astigmatism [clinicaltrials_resource:a137d033324766f64e5df746cab2c137]

country [clinicaltrials_vocabulary:country]

United Kingdom [clinicaltrials_resource:89f9c9f489be2a83cf57e53b9197d288]

download date [clinicaltrials_vocabulary:download-date]

ClinicalTrials.gov processed this data on August 10, 2015

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eligibility [clinicaltrials_vocabulary:eligibility]

eligibility for clinicaltrials:NCT00697190 [clinicaltrials_resource:205bf1088997b310a481bb1b101ce4ab]

firstreceived date [clinicaltrials_vocabulary:firstreceived-date]

2008-06-10T00:00:00Z

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firstreceived results date [clinicaltrials_vocabulary:firstreceived-results-date]

2010-09-09T00:00:00Z

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has expanded access [clinicaltrials_vocabulary:has-expanded-access]

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intervention [clinicaltrials_vocabulary:intervention]

senofilcon A toric [clinicaltrials_resource:1150dba14d6020ee1f514fdc79d729be]

galyfilcon A toric [clinicaltrials_resource:a646ce9f076e0af295f927e5682ed275]

is fda regulated [clinicaltrials_vocabulary:is-fda-regulated]

Yes

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is section 801 [clinicaltrials_vocabulary:is-section-801]

Yes

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lastchanged date [clinicaltrials_vocabulary:lastchanged-date]

2015-05-06T00:00:00Z

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lead sponsor [clinicaltrials_vocabulary:lead-sponsor]

Vistakon [clinicaltrials_resource:5227dfcd66c7062f05bcc5efbac531a9]

location [clinicaltrials_vocabulary:location]

Eurolens Research [clinicaltrials_resource:66909c65c6d21e02d202d854fa3100d6]

nct id [clinicaltrials_vocabulary:nct-id]

NCT00697190

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number of arms [clinicaltrials_vocabulary:number-of-arms]

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org study id [clinicaltrials_vocabulary:org-study-id]

CR-4523

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outcome [clinicaltrials_vocabulary:outcome]

Assessment of Conjunctival Hyperemia in Subjects That Are High Myopes (Have a High Degree of Nearsightedness) [clinicaltrials_resource:NCT00697190/outcome/1]

overall status [clinicaltrials_vocabulary:overall-status]

Completed [clinicaltrials_resource:07ca5050e697392c9ed47e6453f1453f]

oversight [clinicaltrials_vocabulary:oversight]

United Kingdom: Research Ethics Committee [clinicaltrials_resource:abd441b2ecf526a576a948863156e665]

participant flow [clinicaltrials_vocabulary:participant-flow]

participant flow for clinicaltrials:NCT00697190 [clinicaltrials_resource:dbdf85c18846686dee135962b36f2cde]

primary completion date [clinicaltrials_vocabulary:primary-completion-date]

2008-09-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

reported events [clinicaltrials_vocabulary:reported-events]

Reported events for NCT00697190 [clinicaltrials_resource:23a7aa48d2a8bea999efd65f124339c7]

responsible party [clinicaltrials_vocabulary:responsible-party]

[clinicaltrials_resource:dbd41868ee618d3e64daa1adf8c3a8a0]

source [clinicaltrials_vocabulary:source]

Vistakon [clinicaltrials_resource:5227dfcd66c7062f05bcc5efbac531a9]

start date [clinicaltrials_vocabulary:start-date]

2008-05-01T00:00:00Z

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study design [clinicaltrials_vocabulary:study-design]

clinicaltrials:NCT00697190 study design [clinicaltrials_resource:2f3ac1bb17f0dda1d1ab093b85fe5ab9]

study type [clinicaltrials_vocabulary:study-type]

Interventional [clinicaltrials_resource:843ac00ae5d0b7c7defb84fb42c2ce31]

url [clinicaltrials_vocabulary:url]

NCT00697190

verification date [clinicaltrials_vocabulary:verification-date]

2015-05-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

identifier

clinicaltrials:NCT00697190

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title

Clinical Performance of Atypical Contact Lens Powers on Subjects With Astigmatism

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inDataset

clinicaltrials_resource:bio2rdf.dataset.clinicaltrials.R3

type

Clinical Study [clinicaltrials_vocabulary:Clinical-Study]

clinicaltrials resource [clinicaltrials_vocabulary:Resource]

label

Clinical Performance of Atypic ...... m [clinicaltrials:NCT00697190]

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