A Study to Evaluate the Effectiveness of Nicotinamide Riboside and Pterostilbene Treatment to Protect the Kidneys in Patients with Complex Aortic Aneurysm Repair and Aortic Arch Reconstruction

Overview

Información sobre este estudio

The purpose of this study is to determine the effectiveness of Basis™ (Nicotinamide Riboside and Pterostilbene) in preventing acute kidney injury (AKI) among patients undergoing complex aortic aneurysm repair and aortic arch reconstruction.

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:

  • Male or female.
  • Age > 18 years old.
  • Patients who match the criteria for indication of elective open aortic arch replacement or repair:
    • Total arch;
    • Non-total arch.
  • Patients who match the criteria for indication of elective complex aortic aneurysm repair has to respect the following conditions:
    • Patients undergoing complex aortic aneurysm open reconstruction with a suprarenal clamp:
      • thoracoabdominal aortic aneurysms Crawford extent I to IV;
      • abdominal aortic aneurysms of juxtarenal, pararenal, or paravisceral type.
    • For endovascular approach:
      • patients with pararenal or thoracoabdominal aortic aneurysms Crawford extent I to IV and known stage III or IV CKD;
      • patients with pararenal or thoracoabdominal aortic aneurysms Crawford extent I to IV and solitary or single functioning kidney and known stage III or IV CKD.
  • Patients will be allowed to participate in concomitant endovascular aortic stent-graft trials and prospective cohort studies as long as these do not involve another investigational study drug.

General Exclusion Criteria:

  • Unwilling to comply with the follow-up schedule.
  • Inability or refusal to give informed consent by the patient or a legally authorized representative.
  • Pregnant or breastfeeding.
  • Subject who takes multivitamins containing vitamin B3 derivatives in a dose > 200 mg/day.

Clinical / Laboratory Exclusion Criteria:

  • Renal failure defined as eGFR< 15 mL/min/1.73m^2.
  • Patients in permanent Renal Replacement Therapy.
  • Patients with chronic liver disease: Child-Pugh score class B and C.

Medication Exclusion Criteria:

  • Patients in chemotherapy scheme.
  • Patients taking any immunosuppressant, except for corticosteroids.
  • Patients taking any of these well-known P-glycoprotein substrates: digoxin, fexofenadine, indinavir, sirolimus.
    • For some types of P-glycoprotein substrates, subjects will be closely monitored.

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

Bernardo Mendes, M.D.

Cerrado para la inscripción

Contact information:

Anesthesia Clinical Research Unit

(507) 422-0582

More information

Publicaciones

Publications are currently not available
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CLS-20469594

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