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Tracking Information | |||||
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First Received Date † | July 3, 2007 | ||||
Last Updated Date | April 9, 2009 | ||||
Start Date † | June 2007 | ||||
Current Primary Outcome Measures † |
Saliva composition and dental calculus composition | ||||
Original Primary Outcome Measures † | Same as current | ||||
Change History | Complete list of historical versions of study NCT00495989 on ClinicalTrials.gov Archive Site | ||||
Current Secondary Outcome Measures † | |||||
Original Secondary Outcome Measures † | |||||
Descriptive Information | |||||
Brief Title † | Saliva and Dental Calculus in Handicapped People | ||||
Official Title † | The Relationship Between Saliva and Dental Calculus in a Population of Institutionalized Handicapped Persons | ||||
Brief Summary | This is an evaluation of potential differences in saliva composition and dental calculus composition between orally fed and tube fed individuals in an institutional environment. |
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Detailed Description | |||||
Study Phase | |||||
Study Type † | Interventional | ||||
Study Design † | Diagnostic, Open Label, Active Control, Single Group Assignment, Safety Study | ||||
Condition † | Disabled Persons | ||||
Intervention † | Procedure: saliva sampling + dental calculus collection | ||||
Study Arms / Comparison Groups | |||||
Publications * | |||||
* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline. |
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Recruitment Information | |||||
Recruitment Status † | Completed | ||||
Enrollment † | 100 | ||||
Completion Date | September 2008 | ||||
Primary Completion Date | September 2008 (final data collection date for primary outcome measure) | ||||
Eligibility Criteria † | Inclusion Criteria:
Exclusion Criteria:
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Gender | Both | ||||
Ages | 5 Years and older | ||||
Accepts Healthy Volunteers | No | ||||
Contacts †† | |||||
Location Countries † | Belgium | ||||
Expanded Access Status | |||||
Administrative Information | |||||
NCT ID † | NCT00495989 | ||||
Responsible Party | Johan Aps, University Hospital Ghent | ||||
Secondary IDs †† | |||||
Study Sponsor † | University Hospital, Ghent | ||||
Collaborators †† | |||||
Investigators † |
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Information Provided By | University Hospital, Ghent | ||||
Verification Date | April 2009 | ||||
† Required WHO trial registration data element. †† WHO trial registration data element that is required only if it exists. |