Skip to content

Characteristics of Clinical Laboratory Indicators in Patients with Dengue Fever

Observational Study on the Characteristics of Clinical Laboratory Indicators in Patients with Dengue Fever

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06877039
Enrollment
500
Registered
2025-03-14
Start date
2024-08-01
Completion date
2024-12-01
Last updated
2025-03-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dengue Fever

Brief summary

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?

Interventions

OTHERObservational studies did not involve any interventions

Sponsors

Foshan Hospital of Traditional Chinese Medicine
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
WBCFrom January 2024 to December 2024WBC (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.
HGB (Hemoglobin)From January 2024 to December 2024HGB (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.
PLT (Platelet count)From January 2024 to December 2024PLT (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.
ANC (Absolute Neutrophil Count)From January 2024 to December 2024ANC (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.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026