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Intraoperative Neuromonitoring Recording With a Novel SCS Paddle

CompletedNot applicableNCT05045625
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 purpose of this study is to demonstrate safety and efficacy of a new spinal cord stimulation paddle electrode which is able to target the dorsal horns, dorsal nerve roots, and dorsal columns. The research electrode ("Study Electrode") is designed to answer basic physiological clinical research questions. It may inform future device therapy development, but the Study Electrode is not a product that will be marketed or sold. The Investigators believe the protocol is a Non-Significant Risk study answering basic physiological research questions, which may be performed under hospital IRB approval.

Study details

Official title
Effects of Novel SCS Paddle on Intraoperative Neuromonitoring Recording
Interventions
  • Device: HD Study Electrode
Sponsor
Albany Medical College
Start date
2020-01-10
Primary completion
2021-03-20
Sex
All
Age range
from 18 Years to 90 Years
Results posted
Yes, on ClinicalTrials.gov
Countries
United States
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * patients undergoing a spinal cord stimulation procedure for neuropathic pain * must be fluent in English as well as mentally competent to read and answer the questionnaires, as well as complete pain assessment exams. * subjects must be able to give informed consent. Exclusion Criteria: * patients who are not undergoing thoracic spinal cord stimulation for chronic neuropathic pain

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05045625