A Study Using Dynamic Ultrasound to Enhance the Understanding of Carpal Tunnel Syndrome

Overview

Información sobre este estudio

The purpose of this study is to use ultrasound to detect variations in nerve, tendon and subsynovial connective tissue mobility in patients with carpal tunnel syndrome may be useful as functional biomarkers that serve as predictors for treatment response. To test this patients presenting for treatment of carpal tunnel syndrome will be monitored by ultrasound and by clinical assessment before and after non-surgical and surgical treatment.  The clinical outcomes will be alined with the initial ultrasound motion patterns.

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

  • Has clinical symptoms of Carpal Tunnel Syndrome (CTS)
  • Ages 21 to 80
  • Has had numbness or tingling for at least 4 weeks in at least two digits on one hand that include thumb, index, long or radial border of ring finger
  • Has a clinical diagnosis of carpal tunnel syndrome
  • Has had an electrodiagnostic study or EMG? (Does not need to be positive)
  • Able to understand and complete the study questionnaires and medical assessments in English
  • Is clinically indicated for treatment with either a steroid injection or surgery as treatment for their CTS

EXCLUSION CRITERIA

  • Has had previous carpal tunnel release or other volar wrist surgery on the hand
  • Has a known tumor, mass or deformity of the study hand or wrist
  • Has a previous history of steroid injection into the carpal tunnel (injection group only)
  • Has any of the following diagnoses or conditions
    • Cervical radiculopathy
    • Rheumatoid arthritis or other inflammatory arthritis, including gout
    • Osteoarthritis in the wrist
    • Renal failure
    • Sarcoidosis
    • Peripheral nerve disease
    • Diabetes
    • Uncontrolled thyroid disease or other metabolic disorder
      • Thyroid cancer does not exclude
    • Pregnancy
    • Amyloidosis
    • Major trauma (fractures or complete ligamentous tears) to the study hand or wrist
  • Is a prisoner, institutionalized individual or someone who could be considered a vulnerable person, such as an individual with dementia

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

Peter Amadio, M.D.

Cerrado para la inscripción

More information

Publicaciones

Publications are currently not available
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CLS-20204581

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