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ECAP Guided SCS Lead Implantation: an interventional feasibility study

ECAP Guided SCS Lead Implantation: an interventional feasibility study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON21187
Enrollment
30
Registered
2021-07-20
Start date
2021-07-20
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

FBSS

Interventions

Sponsors

St Antonius Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patient has been included for implantation according to standard criteria from the Dutch Neuromodulation Society. 2. Chronic refractory pain as a result of post-laminectomy syndrome (FBSS) for at least 6 months. 3. Patient is >18 years old. 4. Patient is able and willing to comply with the protocol and follow-up. 5. Patient is fluent in the Dutch language. 6. Patient is able to provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patient is under 18 years old 2. Patient is pregnant or nursing 3. Patient is unable to operate the EvokeTM SCS System 4. Patient is an unsuitable candidate for SCS

Design outcomes

Primary

MeasureTime frame
Successful ECAP guided lead placement

Secondary

MeasureTime frame
1. Neurophysiological characterisations and patient reported outcomes

Contacts

Public ContactHarold Nijhuis

St Antonius Hospital

nijhuis9911@hotmail.com0883206947

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)