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EVOKE ECAP-Controlled Lead Placement and Programming in Chronic Pain Patients

NCT05704751 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2026-01-08

No results posted yet for this study

Summary

This study is designed to evaluate the feasibility of using intra-operative ECAP and Late-Response (LR) recordings for confirmation of activating the neuronal target of the dorsal column in a single-stage SCS lead placement procedure. The collected ECAP and LR data will be analysed post-hoc to further evaluate its utility for determining the laterality of lead placement with respect to the physiologic midline of the dorsal column.

Conditions

  • Back Pain Lower Back Chronic
  • Spinal Cord Stimulation

Interventions

DEVICE

spinal cord stimulation

EVOKE ECAP-Controlled Lead Placement and Programming in Chronic Pain Patients

Sponsors & Collaborators

  • Barts & The London NHS Trust

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-10-27
Primary Completion
2026-03-01
Completion
2026-04-01
FDA Device
Yes

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05704751 on ClinicalTrials.gov