- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00688389
Investigation of the Immuno-regulation and Viral Hepatitis Among Patients With or After Dengue Fever Infection
February 27, 2019 updated by: Kaohsiung Medical University Chung-Ho Memorial Hospital
Follow-up the Health Condition , Investigation of the Immuno-regulation , and the Study for Interaction of Viral Hepatitis--- Among Patients With or After Dengue Fever Infection
The study will collect the blood samples from 350 healthy persons and 350 persons infected with dengue fever.
Study Overview
Detailed Description
Research has showed that CLEC5A interacts with dengue virion directly, and is responsible for dengue virus (DV)-induced DAP12 phosphorylation.
Data suggests that CLEC5A is a potential therapeutic target for dengue hemorrhagic fever (DHF)/dengue shock syndrome (DSS).
This project will study the genes of CLEC5A, Mannose receptor, DC-SIGN, NALP, decoy receptor 3 (DcR3), Toll-like receptors(TLRs), and (Nod)-like receptors (NLRs) for both DF and DHF groups.
In addition, serum level of decoy receptor 3 (DcR3) will be tested.
The study will collect the blood samples from 350 healthy persons and 350 persons infected with dengue fever.
Study Type
Observational
Enrollment (Anticipated)
700
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Jih-Jin Tsai, MD
- Phone Number: 5677 886-7-312-1101
- Email: jijits@cc.kmu.edu.tw
Study Locations
-
-
-
Kaohsiung, Taiwan
- Recruiting
- Kaoshing Medical University Chung-Ho Memorial Hospital
-
Contact:
- Jih-Jin Tsai, MD
- Phone Number: 5677 886-7-312-1101
- Email: jijits@cc.kmu.edu.tw
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
The samples are obtained from the Kaohsiung Medical University Chung-Ho Memorial Hospital in Kaohsiung, Taiwan.
Description
Inclusion Criteria:
- Clinical diagnosis of Dengue fever
Exclusion Criteria:
- none
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
healthy
|
case: infected dengue fever people control:healthy people
|
DF
|
case: infected dengue fever people control:healthy people
|
DHF
|
case: infected dengue fever people control:healthy people
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
檢查肝臟、腎臟及其他生化功能,並分析宿主免疫調控及血小板變化機致
Time Frame: 2007/7/1
|
抽血20 c.c 檢查肝臟、腎臟及其他生化功能,並分析宿主免疫調控及血小板變化機致
|
2007/7/1
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
July 1, 2007
Primary Completion (Anticipated)
December 31, 2020
Study Completion (Anticipated)
December 31, 2020
Study Registration Dates
First Submitted
May 28, 2008
First Submitted That Met QC Criteria
May 30, 2008
First Posted (Estimate)
June 2, 2008
Study Record Updates
Last Update Posted (Actual)
February 28, 2019
Last Update Submitted That Met QC Criteria
February 27, 2019
Last Verified
February 1, 2019
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KMUH-IRB-960195_1
- CB9615
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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