Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT05704751 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

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

Study acronym: ECAP
StatusWithdrawn
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

See every version on ClinicalTrials.gov ↗

  1. Stopped Trial status changed: Recruiting → Withdrawn Sponsor's reason: We were unable to recruit any patients for this study. There were processes to add an additional site but due to site capacity, unfortunately we were unable to recruit or transfer. Show 6 more changesShow less
    • Lead sponsor: Barts & The London NHS Trust to Barts & The London NHS Trust
    • Enrollment target: estimated 20 to confirmed 0
    • Primary completion date changed from estimate of Mar 1, 2026 to Aug 12, 2025
    • Eligibility criteria expanded, about 6 words
    • Secondary endpoints: details revised at 4 of 9 entries
    • Site details revised
  2. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Dec 1, 2025 to Oct 27, 2023
    • Site details revised
    v5
  3. Notable Start date: Nov 1, 2025 to Dec 1, 2025v4
  4. Notable Primary completion date: Mar 1, 2024 to Mar 1, 2026
    • Start date: Nov 1, 2023 to Nov 1, 2025
    • Study completion date: Apr 1, 2025 to Apr 1, 2026
    v3
  5. Notable Start date: Apr 1, 2023 to Nov 1, 2023v2
  6. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT05704751
Lead Sponsor Barts & The London NHS Trust
Conditions
(from sponsor)
Back Pain Lower Back Chronic, Spinal Cord Stimulation
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov