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Retrospective Analysis of Laboratory Profile Variations and Population Differences in Chikungunya Fever

Retrospective Analysis of Laboratory Profile Variations and Population Differences in Chikungunya Fever

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600121785
Enrollment
Unknown
Registered
2026-04-02
Start date
2026-04-02
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Chikungunya fever

Interventions

CHIKF Group:None
Non-CHIKF Group:None

Sponsors

Foshan Maternity & Child Healthcare Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.The inclusion criteria for CHIKF group were positive nucleic acid testing results for the chikungunya virus. 2.The inclusion criteria for the Non-CHIKF Group were a negative polymerase chain reaction (PCR) test result for chikungunya virus and the presence of at least one of the three main symptoms: fever, rash, or joint pain.

Exclusion criteria

Exclusion criteria: 1. There is a significant lack of medical records, and essential clinical or laboratory data cannot be obtained. 2. Merge other known acute viral infections that affect the interpretation of laboratory indicators.

Design outcomes

Primary

MeasureTime frame
Blood Routine Test;Test results for Chikungunya virus nucleic acid detection.;—

Countries

China

Contacts

Public ContactWen Qiu

Foshan Maternity & Child Healthcare Hospital,

1914625011@qq.com+86 757 22978574

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 17, 2026