Actively Recruiting

Age: 5Years +
All Genders
ID07007585

Risk Factors for Hospitalization and Transfusion Criteria in Patients With Dengue Virus Infection: A Prospective Observational Study

Led by Jose Ivan Rodriguez de Molina Serrano · Updated on 2025-09-16

100

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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

Brief Title

Risk Factors for Hospitalization and Transfusion Criteria in Patients With Dengue Virus Infection

Who Can Participate

Age: 5Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 25 years or older
  • Laboratory-confirmed dengue infection by NS1 antigen, IgM serology, or PCR
  • First contact at emergency or outpatient services for this illness
  • Signed informed consent by patient or legal guardian
Not Eligible

You will not qualify if you...

  • Co-infection with other arboviruses or COVID-19
  • Pre-existing blood or cancer-related diseases
  • Refusal to sign informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

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

Long-term Monitoring

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

Trial Site Locations

Total: 1 location

1

Clinica Mexico

Piedras Negras, Coahuila, Mexico, 26000

Actively Recruiting

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Research Team

J

JOSE IVAN RODRIGUEZ DE MOLINA SERRANO, MD, MSc, Ph, Specialist

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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