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Blood parameters used to predict severe cases of dengue at a tertiary centre

PREDICTION OF SEVERITY OF DENGUE USING HEMATOLOGICAL PARAMETERS AT A TERTIARY CARE CENTRE - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/10/074768
Enrollment
100
Registered
2024-10-04
Start date
Unknown
Completion date
Unknown
Last updated
2024-10-14

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

Conditions

Health Condition 1: B338- Other specified viral diseases

Interventions

Intervention1: NIL: NIL

Sponsors

Aishwarya Rajan
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients above 18 years of age who give consent and patients with NS1 and/or IgM Dengue positive

Exclusion criteria

Exclusion criteria: Patients who do not give consent and have IgG Dengue positive. Patients who have co-infection with other bacterial or viral etiology

Design outcomes

Primary

MeasureTime frame
Monitor patients since the day of diagnosis to discharge/death and correlate the monocytosis to severity of dengueTimepoint: Day of diagnosis to day of discharge/death—

Secondary

MeasureTime frame
To look for correlation between monocytosis and thrombocytopeniaTimepoint: Day of diagnosis to day of discharge/death—

Countries

India

Contacts

Public ContactAishwarya Rajan

ESIC Medical College and Hospital, Hyderabad

aishwaryarajan29@gmail.com8374443450

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026