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Tracking Information | |||||
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First Received Date † | August 15, 2005 | ||||
Last Updated Date | October 19, 2007 | ||||
Start Date † | January 2006 | ||||
Current Primary Outcome Measures † |
written documentation by MD in medical record acknowledging elevated BP | ||||
Original Primary Outcome Measures † | Same as current | ||||
Change History | Complete list of historical versions of study NCT00130663 on ClinicalTrials.gov Archive Site | ||||
Current Secondary Outcome Measures † |
compliance with interventions | ||||
Original Secondary Outcome Measures † | Same as current | ||||
Descriptive Information | |||||
Brief Title † | Recognition of Abnormal Pediatric Blood Pressures in Primary Care | ||||
Official Title † | Recognition of Abnormal Pediatric Blood Pressures in Primary Care | ||||
Brief Summary | This study will look at general pediatricians' effectiveness at screening children for elevated blood pressure values in the primary care setting. Two new screening tools will be introduced and their effectiveness will be measured against current practice by way of medical chart review. |
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Detailed Description | |||||
Study Phase | |||||
Study Type † | Interventional | ||||
Study Design † | Diagnostic, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study | ||||
Condition † | Hypertension | ||||
Intervention † | Device: PDA blood pressure screening program and chart reminder | ||||
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 † | |||||
Completion Date | October 2007 | ||||
Primary Completion Date | |||||
Eligibility Criteria † | Inclusion Criteria:
Exclusion Criteria:
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Gender | Both | ||||
Ages | 3 Years to 17 Years | ||||
Accepts Healthy Volunteers | Yes | ||||
Contacts †† | |||||
Location Countries † | |||||
Expanded Access Status | |||||
Administrative Information | |||||
NCT ID † | NCT00130663 | ||||
Responsible Party | |||||
Secondary IDs †† | 219405 | ||||
Study Sponsor † | Nationwide Children's Hospital | ||||
Collaborators †† | |||||
Investigators † |
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Information Provided By | Nationwide Children's Hospital | ||||
Verification Date | October 2007 | ||||
† Required WHO trial registration data element. †† WHO trial registration data element that is required only if it exists. |