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Tracking Information | |
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First Received Date † | April 7, 2009 |
Last Updated Date | May 4, 2009 |
Start Date † | July 2009 |
Current Primary Outcome Measures † | |
Original Primary Outcome Measures † | |
Change History | Complete list of historical versions of study NCT00878683 on ClinicalTrials.gov Archive Site |
Current Secondary Outcome Measures † | |
Original Secondary Outcome Measures † | |
Descriptive Information | |
Brief Title † | [Trial of device that is not approved or cleared by the U.S. FDA] |
Official Title † | |
Brief Summary | |
Detailed Description | |
Study Phase | |
Study Type † | |
Study Design † | |
Condition † | |
Intervention † | |
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 † | Withheld |
Enrollment † | |
Completion Date | |
Primary Completion Date | |
Eligibility Criteria † | |
Gender | |
Ages | |
Accepts Healthy Volunteers | |
Contacts †† | |
Location Countries † | |
Expanded Access Status | |
Administrative Information | |
NCT ID † | NCT00878683 |
Responsible Party | Stephen Waller MD, University of Kansas Medical Center |
Secondary IDs †† | |
Study Sponsor † | University of Kansas |
Collaborators †† | |
Investigators † | |
Information Provided By | University of Kansas |
Verification Date | |
† Required WHO trial registration data element. †† WHO trial registration data element that is required only if it exists. |