A Study of Vaginal Microbial Signatures for Women with Refractory Symptoms of Bacterial Vaginosis or Vaginitis

Overview

Información sobre este estudio

Our aim is to establish a correlation between the vaginal microbiome and symptomatic refractory bacterial vaginosis or vaginitis with clinical diagnostic value.  

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:

  • Female patients 18 years of age or older.
  • Patients must have completed a standard screen for infectious communicable diseases (HPV, Gonorrhea and Chlamydia) as part of their evaluation for symptomatic refractory BV or vaginitis.
    • Women enrolled as normal healthy controls may have completed a standard screen for infectious communicable diseases if clinically indicated (HPV, chlamydia, gonorrhea), although not required for study participation.
  • Patient must have undergone standard culture based diagnostics and at least one round of treatment with standard therapies.
  • Patient presenting vaginal symptoms commonly associated with BV or vaginitis that is unresponsive to treatment and for which physician has determined that no additional therapy is available.
  • Normal, healthy women without a history of bacterial vaginosis will be offered enrollment as controls.

Exclusion Criteria 

  • Women who are pregnant or nursing.
  • Vulnerable adults including prisoners, or anyone unable to understand and give informed consent.
  • Patient currently taking or have taken antibiotics in the past 2 weeks.
  • Women enrolled as normal healthy controls must not have a history of recurrent BV or active symptoms of vaginitis at time of study entry.

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

Rochester, Minn.

Investigador principal de Mayo Clinic

Marina Walther-Antonio, Ph.D.

Cerrado para la inscripción

More information

Publicaciones

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CLS-20315199

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