A Study of Quality of Life and Pain Control Before and After Endovascular Renal Denervation in Individuals with Refractory Kidney Pain

Overview

Información sobre este estudio

The purpose of this study is to examine patient reported outcomes including pain, quality of life, depression and impact on kidney blood flow before and after procedure to destroy the pain sensory nerves of the kidneys in patients with untreatable one or two sided kidney pain.

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

  • Must be able to provide informed consent
  • Willing to participate in pain rehabilitation and pain management programs provided here at Mayo Clinic or elsewhere
  • Has had chronic debilitating kidney pain for >6 months
  • Other approaches to pain management will have been appropriately considered and used when indicated and feasible as deemed by the PI
  • Meets objective measures as assessed by opiate dependence or unwillingness to take opiates, partial or full medical disability or decreased quality of life
  • Must be able to travel to site
  • Ideal candidates will have (unilateral or bilateral) single renal arteries and lack a hemodynamically significant renal artery stenosis and presence of suitable renal artery calibers of 4-7mm
  • Screening CT angiogram of renal arteries provides sufficient renal imaging to exclude genitourinary obstruction, tumor, surgically active nephrolithiasis or other clinically significant pathologies associated with kidney pain
    • CTA will specifically delineate renal anatomy and presence of low accessory arteries (not always seen-special imaging cuts will be performed to identify such cases)

Exclusion Criteria

  • Has renal artery anatomy that is ineligible for treatment including
    • Lacks at least one renal artery for each kidney with ≥ 4 mm diameter and with ≥ 20 mm treatable length prior to a significant arterial branch
    • Renal artery stenosis (>50%) or renal artery aneurysm in renal artery
    • A history of prior renal artery intervention including balloon angioplasty or stenting
    • Renal arteries which contain calcification or abnormality which does not allow at least 4 RF ablations
  • Has a confounding medical condition which may adversely affect the safety of the participant in the opinion of the PI
  • Unable to provide informed consent in the opinion of the PI or collaborator

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

Marie Hogan, M.D., Ph.D.

Abierto para la inscripción

Contact information:

Marie Hogan M.D., Ph.D.

(507) 284-2944

Hogan.Marie@mayo.edu

More information

Publicaciones

Publications are currently not available
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CLS-20301666

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