Clinical Presentation of Melioidosis in Head and Neck Region
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Anticipated)
Enrollment
Contacts and Locations
Study Contact
Study Contact
- Name: Pornthep Kasemsiri, M.D.
- Email: Pkasemsiri99@gmail.com
Study Contact Backup
- Name: Kanokkan Mahawerawat, M.D.
- Email: kan_onunu@hotmail.com
Study Locations
-
-
-
Khon Kaen, Thailand, 40002
- Recruiting
- Khon Kaen University
-
Contact:
- Pornthep Kasemsiri, M.D.
- Email: Pkasemsiri99@gmail.com
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients who has the pus culture from head and neck region positive with Burkholderia pseudomallei
Exclusion Criteria:
- No
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Location of infection in head and neck as assess by clinical diagnosis
Time Frame: 5 years
|
These results will be reported as single or multiple site infection in head and neck region.
|
5 years
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Diagnosis as confirm with pus culture
Time Frame: 5 years
|
Assessing the correlation of melioid titer and culture by Pearson statistic
|
5 years
|
|
Number of participants with successful treatment as assess by clinical presentation
Time Frame: 5 years
|
These results will be evaluated as remission or recurrent. The remission mean that fever or pus collection is subside and no presentation with melioidosis again in 5 years. The recurrent mean that participants will present with clinical melioidosis again in 5 years |
5 years
|
Collaborators and Investigators
Sponsor
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Anticipated)
Primary Completion
Study Completion (Anticipated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimate)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- MEC007/59
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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