N/A
N=1,492
The Etiology of Acute Febrile Illness Requiring Hospitalization
Acute Febrile Illness
Bottom Line
View on ClinicalTrials.gov: NCT02763462 ↗Enrolled (actual)
1,492
Serious AEs
0.0%
Results posted
Feb 2023
Primary outcome: Primary: The Etiologies (Bacteria, Viruses, Parasites, Fungi and Others) of Fever Illness Expressed in Percentages of Enrolled Subjects. — 621; 362; 15; 5 Participants
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- —
- Age
- Pediatric, Adult, Older Adult · 1+ yrs
- Sex
- All
- Sponsor
- Ina-Respond
- Primary completion
- Oct 2016
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY The Etiologies (Bacteria, Viruses, Parasites, Fungi and Others) of Fever Illness Expressed in Percentages of Enrolled Subjects. |
621; 362; 15; 5; 483 | — |
| SECONDARY Number of Participants With Affected Organ System by Each Specific Pathogen |
4; 7; 0; 8; 226; 1 | — |
| SECONDARY Number of Participants Enrolled Per Each Clinical Research Site |
269; 213; 65; 91; 201; 257 | — |
| SECONDARY Number of Vials Stored Based on Specimen Type |
7032; 2311; 29; 2; 27; 114 | — |
Summary
This study is an observational cohort study of hospitalized patients with fever. This study will collect demographic data, history of illness, signs and symptoms, results of laboratory tests, clinical course, treatment and outcome. This study conducted at eight INA-RESPOND hospitals. Potential study patients will be any patients (both children and adults).
Eligibility Criteria
Inclusion Criteria
- Age ≥1 year
- Acute febrile illness requiring hospitalization (fever defined as temperature recorded ≥38.0°C during the first 24 hour period of hospitalization).
- Hospitalized within the past 24 hours.
- Willing to allow storage of blood and other specimens for use in future studies of infectious diseases.
Exclusion Criteria
- Hospitalized within the past 3 months, not including current hospitalization for acute febrile illness.
- Inpatient transfer from another hospital.
- A known medical disorder or other circumstance, which in the opinion of the PI might make the participation of the individual unsafe or difficult.
Examples include, but not limited to: mental illness which could affect compliance with protocol, an anemic patient preventing blood draw.
Data sourced from ClinicalTrials.gov (NCT02763462). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.