- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01298206
Case-control Study of Pandemic A/H1N1 Influenza Risk Factors In Lebanon
Study Overview
Status
Conditions
Detailed Description
This study will measure risk and protective factors associated with pandemic A/H1N1 infection. This study will also be able to estimate risk factors for severe illness requiring hospitalization or leading to death. These factors are: travel history, exposure to other confirmed or suspected cases, obesity, pregnancy, influenza vaccination history, residency in nursing homes, attendance of daycares, tobacco use, and other comorbidities (pulmonary diseases, cardiovascular diseases, diabetes, renal insufficiency). Unlike other descriptive studies, this analytical case-control study will enable to accurately measure the strength of association between potential risk factors and outcome. By isolating viruses from specimens collected from cases, this study will be able to characterize these viruses and document any genetic mutations or antiviral resistance.
The main objectives of this study are:
- To investigate the risk factors of infection with the pandemic A/H1N1 viruses.
- To characterize influenza viruses causing infection.
- If enough severe cases were enrolled to make it statistically feasible, this study will investigate the risk factors of severe illness or death associated with infection with the pandemic A/H1N1 viruses.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Beirut, Lebanon, 1107-2020
- American University of Beirut
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Be willing to participate by signing a consent form/assent statement, and completing the study requirements.
- Be willing to provide nasal swab.
- Testing negative for influenza A/H1N1 by RT PCR to be enrolled as a control.
- Testing positive for influenza A/H1N1 by RT PCR to be enrolled as a case.
Exclusion Criteria:
- Any known immunosuppressive condition or immune deficiency disease (including HIV infection), or ongoing receipt of any immunosuppressive therapy. (Note that this study has chosen to exclude such populations because of their increased risk of acquiring infections, they are relatively few, and are not representative of a national sample).
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
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H1N1 not exposed controls
For every enrolled H1N1 case, the study will enroll 2 sex matched controls.
On the date of enrollment of a case, 2 sex-matched controls will be located from the same clinic from which the case was enrolled.
Enrolled controls will then be verified to be free from influenza infection at the time of enrollment by RT-PCR.
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H1N1 exposed Cases
A swab will be collected from cases to verify presence of pandemic influenza.
Testing positive for influenza A/H1N1 by RT PCR to be enrolled will be confirmed as a case.
The participant will be presented with a questionnaire that will capture exposure data through a group of variables assessing underlying health conditions, symptoms, use of influenza vaccine, travel, occupational setting, and other demographic variables.
Cases will be contacted once during the study.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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This study will investigate the risk factors with pandemic A/H1N1 virus by measuring the degree of exposure to virus;
Time Frame: One (1) year
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This study hypothesize that certain factors make people more vulnerable to be infected with A/H1N1, such as traveling to H1N1 infected area, exposure to infected patients, no influenza vaccination, residency in nursing homes, attendance of daycares, poor health and etc.
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One (1) year
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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This study will characterize influenza viruses causing infection by using molecular and cultural techniques
Time Frame: One (1) year
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Through these techniques, the study will isolate and characterize influenza viruses causing infection and morbidity severity of infection among the enrolled cases.
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One (1) year
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This study will investigate the risk factors of severe illness or death associated with infection with the pandemic A/H1N1 viruses.
Time Frame: One (1) year
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This study hypothesizes that certain factors make patients infected with A/H1N1 more vulnerable to severe illness or death, such as obesity, pregnancy, tobacco use, and other co-morbidities (pulmonary diseases, cardiovascular diseases, diabetes, and renal insufficiency).
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One (1) year
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Ghazi Kayali, Ph.D, MPH, St. Jude Children's Research Hospital
Publications and helpful links
Helpful Links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- XPD10-150 PANFLU
- CDRF-BEP-22033 (Other Identifier: Biosecurity Engagement Program, US Department of State)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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