Qualitative and Quantitative HIV RNA Detection in Saliva Using the Oragene RNA Kit
| Tracking Information | |
|---|---|
| First Received Date ICMJE | April 21, 2008 |
| Last Updated Date | April 28, 2011 |
| Start Date ICMJE | October 2007 |
| Primary Completion Date | May 2008 (final data collection date for primary outcome measure) |
| Current Primary Outcome Measures ICMJE | Not Provided |
| Original Primary Outcome Measures ICMJE | Not Provided |
| Change History | Complete list of historical versions of study NCT01344642 on ClinicalTrials.gov Archive Site |
| Current Secondary Outcome Measures ICMJE | Not Provided |
| Original Secondary Outcome Measures ICMJE | Not Provided |
| Current Other Outcome Measures ICMJE | Not Provided |
| Original Other Outcome Measures ICMJE | Not Provided |
| Descriptive Information | |
| Brief Title ICMJE | Qualitative and Quantitative HIV RNA Detection in Saliva Using the Oragene RNA Kit |
| Official Title ICMJE | Qualitative and Quantitative HIV RNA Detection in Saliva Using the Oragene RNA Kit |
| Brief Summary | The purpose of this study is to determine if the Oragene.RNA kit is able to detect HIV RNA in saliva. |
| Detailed Description | There is an important need for a rapid, non-invasive, sensitive and specific method for detection of HIV RNA, particularly in clinical settings in which patients at risk for HIV exposure are assessed and screened. A rapid and non-invasive method for quantitative testing of HIV RNA would be also valuable to monitor suppression of HIV RNA as a primary surrogate marker of combination antiretroviral therapy efficacy. An Ottawa-based biotech company (DNA Genotek Inc) has developed and sells to research and clinical labs world-wide a kit (Oragene� DNA Self-collection kit) that permits the collection, stabilization at room temperature, and purification of DNA present in saliva. They have recently developed a kit (Oragene��RNA) that is purported to stabilize RNA in saliva, a non-invasive source of a biological fluid. |
| Study Type ICMJE | Observational |
| Study Design ICMJE | Observational Model: Cohort Time Perspective: Prospective |
| Target Follow-Up Duration | Not Provided |
| Biospecimen | Not Provided |
| Sampling Method | Non-Probability Sample |
| Study Population | HIV monoinfected HIV-HCV co-infected HIV and HCV uninfected control |
| Condition ICMJE | HIV Infections |
| Intervention ICMJE | Not Provided |
| Study Group/Cohort (s) | Not Provided |
| Publications * | Not Provided |
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* Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline. |
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| Recruitment Information | |
| Recruitment Status ICMJE | Completed |
| Enrollment ICMJE | 40 |
| Completion Date | December 2010 |
| Primary Completion Date | May 2008 (final data collection date for primary outcome measure) |
| Eligibility Criteria ICMJE | Inclusion Criteria:
Exclusion Criteria:
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| Gender | Both |
| Ages | 18 Years and older |
| Accepts Healthy Volunteers | Yes |
| Contacts ICMJE | Contact information is only displayed when the study is recruiting subjects |
| Location Countries ICMJE | Canada |
| Administrative Information | |
| NCT Number ICMJE | NCT01344642 |
| Other Study ID Numbers ICMJE | 2007614-01H |
| Has Data Monitoring Committee | No |
| Responsible Party | Curtis Cooper, OHRI |
| Study Sponsor ICMJE | Ottawa Hospital Research Institute |
| Collaborators ICMJE | DNA Genotek (has supplied the kits) |
| Investigators ICMJE | Not Provided |
| Information Provided By | Ottawa Hospital Research Institute |
| Verification Date | October 2008 |
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ICMJE Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP |
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