- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06877039
Characteristics of Clinical Laboratory Indicators in Patients with Dengue Fever
March 13, 2025 updated by: Qilong Nie, Foshan Hospital of Traditional Chinese Medicine
Observational Study on the Characteristics of Clinical Laboratory Indicators in Patients with Dengue Fever
The objective of this observational study was to understand the changes in laboratory indicators and clinical manifestations of dengue patients at various ages, and to provide new ideas for the treatment and prevention of dengue.
The main questions it aims to answer are: 1 What are the key abnormal items in blood routine indicators of dengue patients? 2 Does dengue affect liver function in patients?
Will there be liver damage?
And when? 3. What are the specific clinical manifestations of dengue patients?
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
500
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Guangdong
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Foshan, Guangdong, China, 528000
- Foshan Hospital of Traditional Chinese Medicine, Guangzhou University of Chinese Medicine, Foshan, 528051, Guangdong, China.
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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
No
Sampling Method
Non-Probability Sample
Study Population
The subjects in this study were dengue fever patients.
Description
Inclusion Criteria**:
- Meet the clinical diagnostic criteria for dengue fever, with blood indicators showing that the dengue antigen is positive.
- No age limit for inclusion.
- Voluntarily agree to participate in the study and sign the informed consent.
- Complete clinical data available, including symptoms and laboratory tests, to support subsequent analysis.
Exclusion Criteria**:
- Incomplete or unavailable clinical data. Patients will be excluded if sufficient laboratory data and symptoms cannot be collected.
- Unable to understand or unwilling to sign the informed consent for any reason.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
WBC
Time Frame: From January 2024 to December 2024
|
WBC (White Blood Cell count), unit: cells/µL.
All these markers will be assessed at baseline (Day 0) and during monthly follow-up visits throughout the study period from January 2024 to December 2024.
Data will be collected and summarized as.
|
From January 2024 to December 2024
|
|
HGB (Hemoglobin)
Time Frame: From January 2024 to December 2024
|
HGB (Hemoglobin), unit: g/dL; All these markers will be assessed at baseline (Day 0) and during monthly follow-up visits throughout the study period from January 2024 to December 2024.
Data will be collected and summarized as.
|
From January 2024 to December 2024
|
|
PLT (Platelet count)
Time Frame: From January 2024 to December 2024
|
PLT (Platelet count), unit: cells/µL; All these markers will be assessed at baseline (Day 0) and during monthly follow-up visits throughout the study period from January 2024 to December 2024.
Data will be collected and summarized as.
|
From January 2024 to December 2024
|
|
ANC (Absolute Neutrophil Count)
Time Frame: From January 2024 to December 2024
|
ANC (Absolute Neutrophil Count), unit: cells/µL.
All these markers will be assessed at baseline (Day 0) and during monthly follow-up visits throughout the study period from January 2024 to December 2024.
Data will be collected and summarized as.
|
From January 2024 to December 2024
|
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 (Actual)
August 1, 2024
Primary Completion (Actual)
December 1, 2024
Study Completion (Actual)
December 1, 2024
Study Registration Dates
First Submitted
February 27, 2025
First Submitted That Met QC Criteria
March 13, 2025
First Posted (Actual)
March 25, 2025
Study Record Updates
Last Update Posted (Actual)
March 25, 2025
Last Update Submitted That Met QC Criteria
March 13, 2025
Last Verified
March 1, 2025
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Foshan Hospital of Traditional
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
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.