Post-operative Dental Pain Study Comparing Two Different Dosage of Analgesic Efficacy

Bio2RDF uri

Post-operative Dental Pain Study Comparing Two Different Dosage of Analgesic Efficacy

http://bio2rdf.org/clinicaltrials:NCT01075243

Bio2RDF identifier

NCT01075243

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Bio2RDF namespace

clinicaltrials

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Bio2RDF uri

http://bio2rdf.org/clinicaltrials:NCT01075243

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identifiers.org URI

NCT01075243

actual enrollment [clinicaltrials_vocabulary:actual-enrollment]

401

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brief summary [clinicaltrials_vocabulary:brief-summary]

GlaxoSmithKline will be ...... atment and Follow up visits).

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brief title [clinicaltrials_vocabulary:brief-title]

Post-operative Dental Pain Study Comparing Two Different Dosage of Analgesic Efficacy

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clinical result [clinicaltrials_vocabulary:clinical-result]

clinical results for clinicaltrials:NCT01075243 [clinicaltrials_resource:b07aad8a18c725fdd6904c2e96a5a09f]

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

Sum of Pain Relief and Pain Intensity Differences From 0 to 6 Hours (SPRID 6 Hours) Every two hours from Baseline to 6 hours post dose [clinicaltrials_resource:219d97d22e0bd2d93e619f7d054b732f]

clinicaltrials_vocabulary:secondary outcome [clinicaltrials_vocabulary:clinicaltrials_vocabulary:secondary-outcome]

Sum of Pain Relief and Pain Intensity Differences From 0 to 6 Hours (SPRID 6 Hours) Every two hours from Baseline to 6 hours post dose [clinicaltrials_resource:0d999e148e750e53a9de5ecde8896578]

Sum of Pain Relief and Pain Intensity Differences From 0 to 6 Hours (SPRID 6 Hours) Every two hours from Baseline to 6 hours post dose [clinicaltrials_resource:26a8fdc99154c4c36b505caef39cdadf]

Sum of Pain Relief and Pain Intensity Differences From 0 to 6 Hours (SPRID 6 Hours) Every two hours from Baseline to 6 hours post dose [clinicaltrials_resource:3fe0f414bfee74d77c1b05ad840bda95]

Sum of Pain Relief and Pain Intensity Differences From 0 to 6 Hours (SPRID 6 Hours) Every two hours from Baseline to 6 hours post dose [clinicaltrials_resource:663b2d6d8fdab901fd04272144045ab0]

Sum of Pain Relief and Pain Intensity Differences From 0 to 6 Hours (SPRID 6 Hours) Every two hours from Baseline to 6 hours post dose [clinicaltrials_resource:84cc28d5f2999d30a2b8ef959a44e85c]

Sum of Pain Relief and Pain Intensity Differences From 0 to 6 Hours (SPRID 6 Hours) Every two hours from Baseline to 6 hours post dose [clinicaltrials_resource:856dbb24eeb9596b79300905cf2486d7]

Sum of Pain Relief and Pain Intensity Differences From 0 to 6 Hours (SPRID 6 Hours) Every two hours from Baseline to 6 hours post dose [clinicaltrials_resource:8e64417ee43b968c59eefd65fe663a65]

Sum of Pain Relief and Pain Intensity Differences From 0 to 6 Hours (SPRID 6 Hours) Every two hours from Baseline to 6 hours post dose [clinicaltrials_resource:a9f9467b8ed25d468841f54fe45555db]

Sum of Pain Relief and Pain Intensity Differences From 0 to 6 Hours (SPRID 6 Hours) Every two hours from Baseline to 6 hours post dose [clinicaltrials_resource:ae31e441389dd7d3a40714ea8bcbae00]

Sum of Pain Relief and Pain Intensity Differences From 0 to 6 Hours (SPRID 6 Hours) Every two hours from Baseline to 6 hours post dose [clinicaltrials_resource:b24299a5dce6461b990eed24f0a05343]

completion date [clinicaltrials_vocabulary:completion-date]

2010-03-01T00:00:00Z

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condition [clinicaltrials_vocabulary:condition]

Post-surgical Dental Pain [clinicaltrials_resource:d7ad314886e371008c55d2b360defad7]

condition browse [clinicaltrials_vocabulary:condition-browse]

Toothache [clinicaltrials_resource:6b9a412f7008f6b612bf660bfb87de35]

condition mesh [clinicaltrials_vocabulary:condition-mesh]

Toothache [clinicaltrials_resource:6b9a412f7008f6b612bf660bfb87de35]

country [clinicaltrials_vocabulary:country]

United States [clinicaltrials_resource:f253efe302d32ab264a76e0ce65be769]

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:NCT01075243 [clinicaltrials_resource:ce49cdad797b4715cf96931fc0730da4]

firstreceived date [clinicaltrials_vocabulary:firstreceived-date]

2010-02-23T00:00:00Z

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

2013-06-20T00:00:00Z

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

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intervention [clinicaltrials_vocabulary:intervention]

Paracetamol 1000 mg [clinicaltrials_resource:3f00a653895a4334e48b745d1a4cbcd3]

Placebo [clinicaltrials_resource:abc0de84dd8b99b5bd67881a26602098]

Paracetamol 650 mg [clinicaltrials_resource:cb3dd3e4be01f14ec98e111b33c8b2c2]

intervention browse [clinicaltrials_vocabulary:intervention-browse]

Acetaminophen [clinicaltrials_resource:07d0794b3920eb10ad4ec997fda344fb]

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

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

keyword [clinicaltrials_vocabulary:keyword]

Post-surgical dental pain

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

dental pain

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paracetamol

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

lastchanged date [clinicaltrials_vocabulary:lastchanged-date]

2015-04-27T00:00:00Z

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lead sponsor [clinicaltrials_vocabulary:lead-sponsor]

GlaxoSmithKline [clinicaltrials_resource:8075d9d563cbe75004e7b6c2c4360b29]

location [clinicaltrials_vocabulary:location]

Jean Brown Research [clinicaltrials_resource:f7a502ba8c3fada48e7bb31781fe97f1]

nct id [clinicaltrials_vocabulary:nct-id]

NCT01075243

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

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

official title [clinicaltrials_vocabulary:official-title]

A Study to Compare the Analges ...... by Post-operative Pain Relief

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

A4000685

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outcome [clinicaltrials_vocabulary:outcome]

Sum of Pain Relief and Pain Intensity Differences From 0 to 6 Hours (SPRID 6 Hours) [clinicaltrials_resource:NCT01075243/outcome/1]

overall official [clinicaltrials_vocabulary:overall-official]

GSK Clinical Trials [clinicaltrials_resource:482ca15ed5613e7d70d0185ac9204ca5]

overall status [clinicaltrials_vocabulary:overall-status]

Completed [clinicaltrials_resource:07ca5050e697392c9ed47e6453f1453f]

oversight [clinicaltrials_vocabulary:oversight]

United States: Institutional Review Board [clinicaltrials_resource:b46c5f1ee626ee51e33e6c048a7b19f6]

participant flow [clinicaltrials_vocabulary:participant-flow]

participant flow for clinicaltrials:NCT01075243 [clinicaltrials_resource:3ad314e3b91b93854f31aa36ff695fc9]

phase [clinicaltrials_vocabulary:phase]

Phase 4 [clinicaltrials_resource:ec41833bc88cd90619c4d85c549688bd]

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

2010-03-01T00:00:00Z

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

reported events [clinicaltrials_vocabulary:reported-events]

Reported events for NCT01075243 [clinicaltrials_resource:28d0b1a4010f442d991762aa5f5367d8]

responsible party [clinicaltrials_vocabulary:responsible-party]

[clinicaltrials_resource:dbd41868ee618d3e64daa1adf8c3a8a0]

source [clinicaltrials_vocabulary:source]

GlaxoSmithKline [clinicaltrials_resource:8075d9d563cbe75004e7b6c2c4360b29]

start date [clinicaltrials_vocabulary:start-date]

2009-11-01T00:00:00Z

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study design [clinicaltrials_vocabulary:study-design]

clinicaltrials:NCT01075243 study design [clinicaltrials_resource:aa30034368b2e40bee5744e8c0616a70]

study type [clinicaltrials_vocabulary:study-type]

Interventional [clinicaltrials_resource:843ac00ae5d0b7c7defb84fb42c2ce31]

url [clinicaltrials_vocabulary:url]

NCT01075243

verification date [clinicaltrials_vocabulary:verification-date]

2015-04-01T00:00:00Z

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

identifier

clinicaltrials:NCT01075243

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