A Study to Evaluate Biomarkers of Fluoroquinolone-induced Mitochondrial Toxicity

Overview

Información sobre este estudio

The purposes of this study are to determine if patients treated with fluoroquinolone (FQ) antibiotics have depletion of mitochondrial DNA (mtDNA) in buccal swab samples, and whether the degree of depletion correlates with the likelihood of developing FQ-associated toxicity.

2nd arm - An additional group of patients will be enrolled if they previously received FQ antibiotics. appear to be symptomatic and have a previously collected muscle or nerve biopsy for clinical purposes available for this research study. 

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:

Arm 1:

  • Treatment with oral and/or intravenous FQ antibiotics (ciprofloxacin, levofloxacin, moxifloxacin, delafloxacin) that has been initiated upon, or within 24 hours of, admission to the HIM service or at time of initial Infectious Diseases consultation and lasting > 48 hours.

Arm 2:

  • Previously received FQ antibiotics in the past and symptomatic.

Exclusion Criteria: 

Arm 1 - any of the following:

  • FQ antibiotic treatment that has been initiated > 24 hours prior to admission that has not yet been completed (e.g., patient is admitted or transferred to HIM or had ID consult when they are already on day 3 of a 7-day course of treatment);
  • Active cancer;
  • Chemotherapy or radiation therapy within the past 6 months;
  • Physical and/or cognitive impairment to the extent that patient cannot be fully assessed for or asked about symptoms of adverse reactions associated with fluoroquinolones;
  • Currently pregnant;
  • Blood transfusion within the past 4 months;
  • Previous bone marrow or organ transplant;
  • currently on nucleoside reverse transcriptase inhibitors;
  • Pre-existing mitochondrial disease;
  • < 18 years of age; 
  • Prior treatment with FQs within 1 week of admission;
  • Active history of routine alcohol use.

Arm 2:

  • Previously received FQ antibiotics in the past and not symptomatic.

PLEASE NOTE:   At this time, only Arm 2 is open to enrollment at Mayo Clinic.

Eligibility last updated 6/2/23. 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

Rochester, Minn.

Investigador principal de Mayo Clinic

Linda Hasadsri, M.D., Ph.D.

Abierto para la inscripción

Contact information:

Lisa Hines

(507) 266-1710

Hines.Lisa@mayo.edu

More information

Publicaciones

Publications are currently not available
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CLS-20464386

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