Evaluating Kidney Stones To Determine If They Lead to Kidney Disease

Overview

Información sobre este estudio

We hypothesize that clinical studies to investigate the role of individual proteins in kidney stone pathogenesis have likely been confounded by an unknown variety of underlying renal pathologies. Therefore, we propose to examine urinary protein crystallization inhibitors in patient populations that have been carefully phenotyped relative to renal stone precursor lesions by direct endoscopic visualization. In collaboration with Project #1, our second major goal is to use these accurately phenotyped patients in order to adapt modern dual-energy CT technology to develop a reliable noninvasive technique to accurately and noninvasively determine stone composition and visualize the earliest kidney stone precursor lesions. Our long-term goal is to improve CT technology so that it can be used to allow large-scale clinical protocols of accurately phenotyped, hence, homogeneous, patient populations.

In a subset we will sample sterile stone, dental plaque, blood and urine samples for detailed microbiome analysis in order to determine the contribution of micro organisms to stone pathogensis.

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:       

  • Patients undergoing percutaneous nephrolithotomy or ureteroscopy for treatment of symptomatic renal or proximal ureteral stones without evidence of pyelonephritis will be included. 
  • Control patients will be those individuals undergoing percutaneous, ureteroscopic or nephrectomy for non-stone related indications.

Exclusion Criteria:      

  • Pregnant patients are not eligible for this protocol, and would not generally have invasive stone removal procedures. 
  • All women of child bearing age will have pregnancy testing as part of their routine clinical care.

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

John Lieske, M.D.

Abierto para la inscripción

Contact information:

Angela Waits CCRP

(507) 266-5293

Waits.Angela@mayo.edu

More information

Publicaciones

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