APM in the Evoke SCS System to Program Patients With Chronic Pain of the Trunk and/or Limbs

Saluda Medical

Status: Completed

Conditions: Chronic Pain; Pain, Chronic

Treatments: Device: APM

Study type: Interventional

Funder types: Industry

Identifiers

NCT06057480

D103684

Details and patient eligibility

About

Study to evaluate the use of the Assisted Programming Module (APM) in the Evoke Spinal Cord Stimulation (SCS) System to program patients with chronic pain of the trunk and/or limbs.

Enrollment: 30 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Subject has or is planning to undergo a temporary trial with Evoke System within the FDA approved indication.
• Subject is willing and capable of giving informed consent and able to comply with study-related requirements.

Exclusion criteria

• There are no exclusion criteria.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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30 participants in 1 patient group

APM

Experimental group

Description:

Investigational programming software module, the Assisted Programming Module (APM)

Treatment:

Device: APM