Phase
Condition
Respiratory Syncytial Virus (Rsv) Infection
Treatment
MeMed BV® biomarker test
Usual care
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Current disease duration ≤ 7 days
Temperature ≥ 37.8°C (100°F) or tactile fever, noted at least once within the last 7days
Clinical suspicion of bacterial or viral respiratory tract infection (RTI)
Blood tests are being ordered
Exclusion
Exclusion Criteria:
Systemic antibiotics taken up to 48 hours prior to presentation
Outpatient steroids taken within 48 hours prior to presentation
Suspicion and/or confirmed diagnosis of infectious gastroenteritis/colitis
Inflammatory disease
Congenital immune deficiency (CID)
A proven or suspected infection on the presentation with Mycobacterial ,parasitic orfungal (e.g., Candida, Histoplasma, Aspergillus) pathogen
Human immunodeficiency virus(HIV), Hepatitis B Virus (HBV), or Hepatitis C Virus (HCV) infection (self-declared or known from medical records)
Major trauma and/or burns in the last 7 days
Major surgery in the last 7 days
Pregnancy - Self reported or medically confirmed
Active malignancy - Cancer diagnosed within the previous six months, recurrent,regionally advanced, or metastatic cancer, cancer for which treatment had beenadministered within six months, or hematological cancer that is not in completeremission.
Current treatment with immune-suppressive or immune-modulating therapies, at somepoint in the past 10 days
Hemodynamically unstable (require life-saving interventions such as vasopressors)
Patients transferred from another facility who already have a differentiatedrespiratory illness (known diagnosis e.g., culture positive results)
Consider unsuitable for the study by the study team
Study Design
Study Description
Connect with a study center
The University of Texas Health Science Center at Houston
Houston, Texas 77030
United StatesActive - Recruiting
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