Skip to content

Patient Experience Comparing Tonic Vs. Burst Spinal Cord Stimulation For Chronic Pain

TerminatedNot applicableNCT04159753
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)

Researchers are evaluating if subjects who have already experienced tonic spinal cord stimulation would have a better pain relief status with burst spinal cord stimulation.

Study details

Official title
An Evaluation Study of Patient Experience Comparing Tonic Vs. Burst Spinal Cord Stimulation For Chronic Pain
Conditions
Sponsor
Mayo Clinic
Start date
2019-10-10
Primary completion
2021-04-14
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: * Males and females ≥18 years-old * Diagnosed with chronic pain * Have an already-implanted Eon Family IPG for a minimum period of 6 months * Are interested in trying burst technology by reprograming their IPG for 2-3 weeks according to the 30-Day Trial standard of care * Signed informed consent Exclusion Criteria: * Subject's overall Beck Depression Inventory II Score is \>24 or has a score of 3 on question 9 relating to suicidal thoughts or wishes at the screening visit; If subjects scores indicate suicidal thoughts, subject is going to be evaluated further if they will be subjects to Baker's act * Subject is currently receiving, applying or considering seeking disability payments, workers compensation, or is involved in disability litigation * Subject has an infusion pump or any other implantable neurostimulator device * Subjects with a separate, concurrent, clinically significant or disabling chronic pain problem that requires additional medical or surgical treatment * Subject's pain originates from peripheral vascular disease * Subject is immunocompromised * Subject has a documented history of substance abuse (narcotics, alcohol, etc.) or substance dependency in the 6 months prior to baseline data collection * Subject has history of cancer requiring active treatment in the last 6 months * Pregnancy

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT04159753