Early Identification of Pulmonary Coccidioidomycosis

Overview

Información sobre este estudio

The purpose of this study is to identify, recruit, and enroll patients with community-acquired pneumonia (CAP) to collect their blood, sputum, urine, and a nasopharyngeal swab for specimen storage. The study also aims to develop a biomarker assay to detect circulating antigen in patients infected with Coccidioides.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

 Inclusion Criteria:                                                                  

  • Community acquired pneumonia: one of the following:
    • CXR or CT evidence of pulmonary infiltrate;
    • Clinical impression as documented by physician or advanced practice provider.
  • Symptom duration not longer than 14 days.
  • Age ≥18 years.
  • Inpatient or Outpatient.

 Exclusion Criteria:

  • Known prior coccidioidal illness (prior to onset of current illness):
    • Known prior coccidioidal history;
    • Known prior positive coccidioidal skin test;
    • Known prior coccidioidal serology in past.        
  • Health-care associated pneumonia:
    • Hospitalization in an acute care hospital for ≥ 2 days within 90 days of current infection;
    • Residence in nursing home or long-term care facility;
    • Recent IV antibiotic therapy, chemotherapy or wound care ≤ 30 days prior to current infection, given for a pneumonia indication;
    • Attended a hemodialysis clinic within 30 days.
  • Active COVID-19 infection (i.e., positive PCR or antigen test in the previous 4 months for which symptoms had yet to resolve.  Persistent symptoms (fever, cough, headache, chest pain, shortness of breath) that are unresolved are grounds for exclusion.
  • No exclusions for underlying health problems other than the above. Patients with underlying immunosuppression will be enrolled only as a subset of total patients enrolled.  Acceptable underlying immunosuppression will be defined as the receipt of immunosuppressive medications (within ≤ 3 months) such as but not limited to systemic corticosteroids greater than or equal to an equivalent dose of prednisone 5 milligrams daily, calcineurin inhibitors (tacrolimus, etc.), mycophenolate mofetil, rapamycin, others.

Eligibility last updated 10/5/21. Questions regarding updates should be directed to the study team contact.

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Scottsdale/Phoenix, Ariz.

Investigador principal de Mayo Clinic

Janis Blair, M.D.

Cerrado para la inscripción

Contact information:

Sonia Velazquez

(480) 342-6677

Robertson.Sonia@mayo.edu

More information

Publicaciones

Publications are currently not available
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CLS-20309527

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