RecruitingNot ApplicableNCT05537662

External Sensing and Neuromodulation to Assess Diabetic Pain Outcomes (XANADO)

External Sensing and Neuromodulation to Assess Diabetic Pain Outcomes


Sponsor

Abbott Medical Devices

Enrollment

30 participants

Start Date

Jun 6, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

This is a prospective, longitudinal, single-center, non-randomized, open-label, post-market clinical feasibility study to assess the efficacy of neuromodulation therapies (SCS and DRG) for chronic pain patients with diabetes and investigate whether physical and physiological data collected from diabetic and pre-diabetic chronic pain patients is predictive of subjective patient-reported outcomes (PROs) and of adjustments in patient care. These assessments will be made prior to, during, and after the trial of the SCS or DRG system. The study will be carried out in the United States at a single site.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called Standard of care neuromodulation therapy (SCS or DRG) for people with chronic pain. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICEStandard of care neuromodulation therapy (SCS or DRG)

Standard SCS or DRG therapy


Locations(1)

Rush University Medical Center

Chicago, Illinois, United States

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NCT05537662


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