Early clinical and laboratory indicators of acute dengue illness.
S Kalayanarooj, D W Vaughn, S Nimmannitya...
https://pubmed.ncbi.nlm.nih.gov/9237695Actively Recruiting
Led by Jose Ivan Rodriguez de Molina Serrano · Updated on 2025-09-16
100
Participants Needed
1
Research Sites
4 weeks
Total Duration
Researchers are studying patients with confirmed dengue virus infection to identify clinical and laboratory factors that may increase the risk of hospitalization. The study also aims to understand how blood transfusions are used in real-world practice and to improve criteria for hospital admission based on observed predictors. This is a prospective observational study conducted over three years at a hospital in northern Mexico. Patients aged 5 years and older who have a confirmed dengue infection and present to the emergency department or outpatient clinic are followed from their initial visit until their illness resolves or they are discharged from the hospital. No experimental treatments are given; patients receive standard medical care. Data collected include symptoms such as fever duration, bleeding, vomiting, abdominal pain, platelet counts, hematocrit levels, and transfusion records. Physicians make transfusion decisions independently, and the reasons for these decisions are recorded. Participants will be monitored through clinical evaluations and laboratory tests during their illness. Researchers will analyze this information to identify factors linked to hospitalization and transfusion needs within 10 to 14 days of symptom onset. The study will track the proportion of patients admitted to the hospital and those who receive blood transfusions. The total participation lasts from the first healthcare contact to clinical recovery or discharge, providing insights into dengue management and patient outcomes.
CONDITIONS
Risk Factors for Hospitalization and Transfusion Criteria in Patients With Dengue Virus Infection
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Complete this quick 3-step screening to check your eligibility
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 14 days from symptom onset
Participants with confirmed dengue infection are observed to collect clinical and laboratory data to identify risk factors for hospitalization and transfusion needs.
Visits at emergency department or outpatient clinic as needed during illness
Duration - Up to 3 years
Participants are followed prospectively for up to 3 years to understand outcomes related to dengue infection and transfusion criteria based on real-world clinical decisions.
Follow-up visits scheduled as per clinical care
Total: 1 location
1
Clinica Mexico
Piedras Negras, Coahuila, Mexico, 26000
Actively Recruiting
J
JOSE IVAN RODRIGUEZ DE MOLINA SERRANO, MD, MSc, Ph, Specialist
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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S Kalayanarooj, D W Vaughn, S Nimmannitya...
https://pubmed.ncbi.nlm.nih.gov/9237695