Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Saluda Medical Americas, Inc.
Age
18–80
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Subject is male or female between the ages of 18 and 80 years.
Have been diagnosed with chronic, intractable pain of the trunk and/or limbs, which has been refractory to conservative therapy for a minimum of 6 months.
Be an appropriate candidate for an SCS trial and the surgical procedures required in this study based on the clinical judgment of the Investigator.
Be willing and capable of giving informed consent and able to comply with study-related requirements, procedures, and visits.
You may not be if
Have a medical condition or pain in other area(s), not intended to be treated with SCS, that could interfere with study procedures, accurate pain reporting, and/or confound evaluation of study endpoints, as determined by the Investigator.
Have evidence of an active disruptive psychological or psychiatric disorder or other known condition significant enough to impact perception of pain, compliance of intervention, and/or ability to evaluate treatment outcomes.
Have an existing drug pump and/or SCS system or another active implantable device such as a pacemaker, deep brain stimulator (DBS), or sacral nerve stimulator (SNS).
Have prior experience with SCS.
Have an active systemic infection or local infection in the area of the surgical site.
Be pregnant or nursing (if female and sexually active, subject must be using a reliable form of birth control, be surgically sterile, or be at least 2 years post-menopausal).
Be concomitantly participating in another clinical study.
Clareo Health | Safety and Efficacy Study of the Evoke™ SCS System With Feedback vs. Conventional Stimulation
