Multicenter Outcome Registry of AnaLgesic Effect of SCS(MORALES) Registry Protocol

Cardio Surgical Partners

Status: Enrolling

Conditions: SCS

Treatments: Device: SCS

Study type: Observational

Funder types: NETWORK

Identifiers

NCT04548375

PainReg

Details and patient eligibility

About

The objective is to provide information to help the physician community decide the most effective type of device/therapy that would work for their patients, based off of the etiology of pain, the location of the pain for sustained pain relief.

Full description

This registry will enroll patients that qualify for an SCS implant, for approved pain areas, as defined by medicare guidelines, and follow these patients for up to 12 months for denovo implants. For patients who have lost their pain relief over time, with a prior implanted device, this registry will follow a change out to another vendor/therapy, and follow those patients for up to 12 months.

Enrollment: 500 estimated patients

Sex: All

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• FDA approved indications for SCS implants, for commercial and government(medicare, medi-cal etc) approved payors

Exclusion criteria