A Six Month Clinical Study Based in the US to Evaluate the Efficacy and Tolerability of Sodium Bicarbonate Toothpaste and Its Effect on Opportunistic or Resistant Organisms [clinicaltrials:NCT02207400]

Bio2RDF identifier

NCT02207400

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Bio2RDF namespace

clinicaltrials

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Bio2RDF uri

http://bio2rdf.org/clinicaltrials:NCT02207400

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identifiers.org URI

NCT02207400

actual enrollment [clinicaltrials_vocabulary:actual-enrollment]

235

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arm group [clinicaltrials_vocabulary:arm-group]

NCT02207400 arm group 89a1b793976935e6bfad3d72d2c6a6f3 [clinicaltrials_resource:NCT02207400/arm-group/89a1b793976935e6bfad3d72d2c6a6f3]

NCT02207400 arm group e66249353461edd12f3e24d6f765064c [clinicaltrials_resource:NCT02207400/arm-group/e66249353461edd12f3e24d6f765064c]

authority [clinicaltrials_vocabulary:authority]

clinicaltrials_resource:d942c8692d257084abf3ac87279faff6

brief summary [clinicaltrials_vocabulary:brief-summary]

This study will compare ...... rnal recruitment agency

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brief title [clinicaltrials_vocabulary:brief-title]

A Six Month Clinical Study Bas ...... unistic or Resistant Organisms

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

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

Evaluation and comparison of Gingival Bleeding (as assessed by number of bleeding sites) following twice daily use of a sodium bicarbonate experimental dentifrice compared to a 0% sodium bicarbonate experimental dentifrice toothpaste after 24 weeks. 24 weeks [clinicaltrials_resource:3eb46e9d3420eb57e6a8139d3abb8eea]

Evaluation and comparison of Gingival Bleeding (as assessed by number of bleeding sites) following twice daily use of a sodium bicarbonate experimental dentifrice compared to a 0% sodium bicarbonate experimental dentifrice toothpaste after 24 weeks. 24 weeks [clinicaltrials_resource:9f06d13f448d371228acfd1b4603b596]

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

Evaluation and comparison of Gingival Bleeding (as assessed by number of bleeding sites) following twice daily use of a sodium bicarbonate experimental dentifrice compared to a 0% sodium bicarbonate experimental dentifrice toothpaste after 24 weeks. 24 weeks [clinicaltrials_resource:0da08df2b3cbfa1ff0162099f26734d7]

Evaluation and comparison of Gingival Bleeding (as assessed by number of bleeding sites) following twice daily use of a sodium bicarbonate experimental dentifrice compared to a 0% sodium bicarbonate experimental dentifrice toothpaste after 24 weeks. 24 weeks [clinicaltrials_resource:3193d39e27e880eef25ba441c318ae3a]

Evaluation and comparison of Gingival Bleeding (as assessed by number of bleeding sites) following twice daily use of a sodium bicarbonate experimental dentifrice compared to a 0% sodium bicarbonate experimental dentifrice toothpaste after 24 weeks. 24 weeks [clinicaltrials_resource:6f5629223190c48d07c29f011f48745a]

Evaluation and comparison of Gingival Bleeding (as assessed by number of bleeding sites) following twice daily use of a sodium bicarbonate experimental dentifrice compared to a 0% sodium bicarbonate experimental dentifrice toothpaste after 24 weeks. 24 weeks [clinicaltrials_resource:87766c4d0e39bffaedf45b5682e26166]

Evaluation and comparison of Gingival Bleeding (as assessed by number of bleeding sites) following twice daily use of a sodium bicarbonate experimental dentifrice compared to a 0% sodium bicarbonate experimental dentifrice toothpaste after 24 weeks. 24 weeks [clinicaltrials_resource:c48c00120ba13ad4734468d15472741f]

completion date [clinicaltrials_vocabulary:completion-date]

2015-02-01T00:00:00Z

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

condition [clinicaltrials_vocabulary:condition]

Oral Hygiene [clinicaltrials_resource:f1e70351fc3c2a1016094bf07ca577de]

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:NCT02207400 [clinicaltrials_resource:05d2d618cd2a69d50192a1b2db837108]

firstreceived date [clinicaltrials_vocabulary:firstreceived-date]

2014-07-21T00:00:00Z

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

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

No

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

intervention [clinicaltrials_vocabulary:intervention]

Sodium bicarbonate plus sodium fluoride [clinicaltrials_resource:aa23a3f620ceef0058e1c469c46a210b]

Sodium fluoride [clinicaltrials_resource:af5e09f9673475d18553e15300d6f07e]

intervention browse [clinicaltrials_vocabulary:intervention-browse]

Listerine [clinicaltrials_resource:45b212be939bf823f56bf04d55c4ef0b]

Sodium Fluoride [clinicaltrials_resource:a0d4a21f0f686612aeaed04efba16753]

Fluorides [clinicaltrials_resource:b0e8a9e293a7893a9be190ab1b6db5f0]

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

No

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

lastchanged date [clinicaltrials_vocabulary:lastchanged-date]

2015-06-04T00:00:00Z

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

lead sponsor [clinicaltrials_vocabulary:lead-sponsor]

GlaxoSmithKline [clinicaltrials_resource:8075d9d563cbe75004e7b6c2c4360b29]

location [clinicaltrials_vocabulary:location]

GSK Investigational Site [clinicaltrials_resource:19b7c48b6e715737daebd296d59325e9]

nct id [clinicaltrials_vocabulary:nct-id]

NCT02207400

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

2

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official title [clinicaltrials_vocabulary:official-title]

A Six Month Clinical Study Bas ...... unistic or Resistant Organisms

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

202,193

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

2015-02-01T00:00:00Z

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responsible party [clinicaltrials_vocabulary:responsible-party]

[clinicaltrials_resource:dbd41868ee618d3e64daa1adf8c3a8a0]

secondary id [clinicaltrials_vocabulary:secondary-id]

RH02434

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source [clinicaltrials_vocabulary:source]

GlaxoSmithKline [clinicaltrials_resource:8075d9d563cbe75004e7b6c2c4360b29]

start date [clinicaltrials_vocabulary:start-date]

2014-08-01T00:00:00Z

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

study design [clinicaltrials_vocabulary:study-design]

clinicaltrials:NCT02207400 study design [clinicaltrials_resource:87ebd4cacbf7645d7e4f99442b9e0038]

study type [clinicaltrials_vocabulary:study-type]

Interventional [clinicaltrials_resource:843ac00ae5d0b7c7defb84fb42c2ce31]

url [clinicaltrials_vocabulary:url]

NCT02207400

verification date [clinicaltrials_vocabulary:verification-date]

2015-06-01T00:00:00Z

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

identifier

clinicaltrials:NCT02207400

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

title

A Six Month Clinical Study Bas ...... unistic or Resistant Organisms

@en

inDataset

clinicaltrials_resource:bio2rdf.dataset.clinicaltrials.R3

type

Clinical Study [clinicaltrials_vocabulary:Clinical-Study]

clinicaltrials resource [clinicaltrials_vocabulary:Resource]

label

A Six Month Clinical Study Bas ...... s [clinicaltrials:NCT02207400]

@en