EVA: Evaluation of EVOKE Therapy Metrics Generated Using the Evoke System With EVA
Not yet recruitingNCT07267715
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
The Evoke Spinal Cord Stimulator (SCS) System (Evoke® System) is an FDA-approved device that is used to manage long lasting, severe pain that is not relieved by typical medical treatments. This research registry is being conducted to collect data from patients treated with a SCS device in order to determine how the device impacts their chronic pain condition. Specifically, the study aims to: * Evaluate data collected from the SCS system on how well the system is working. * Evaluate the feasibility of programming the SCS system independently without external assistance. * Evaluate changes in physical function, fatigue, pain interference, mood, sleep, daily activities, pain control, and overall satisfaction with the device.
Study details
- Official title
- EVA: Evaluation of EVOKE Therapy Metrics Generated Using the Evoke System With EVA
- Conditions
- Interventions
- Device: Spinal Cord Stimulation (SCS) System
- Sponsor
- Dustin Reynolds, MD
- Collaborators
- Saluda Medical Pty Ltd
- Organization
- Mount Carmel Health System
- Start date
- 2025-11-30
- Primary completion
- 2026-11-01
- Sex
- All
- Age range
- from 18 Years
- Results posted
- No results posted in this snapshot
- Countries
- United States
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Subject is not pregnant and 18 years of age or older at the time of enrollment. * Subject has a minimum NRS score of 6 or higher (where 10 indicates the worst imaginable pain) in primary area of pain at baseline. * Subject is planning to have a temporary trial with the Evoke® System to aid in the management of chronic intractable pain of the trunk and/or limbs. * Subject is willing to program the Evoke® System using EVA™ under the supervision of the study investigator or Qualified Health Professional. * Subject is being trialed with a neurostimulation system for the first time. * Subject is able to read and understand English. * Subject is capable of subjective evaluation; subject must be able to describe and rate his/her pain levels. * Subject is willing and capable of giving informed consent. * Subject is willing and able to comply with study-related requirements, procedures, and visits. * Subject has adequate cognitive ability to use a patient programmer and recharger as determined by the Investigator. Exclusion Criteria: \- There are no exclusion criteria for this study.
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07267715