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Not yet recruiting NCT07354243

International Neuromodulation Registry

— Observational Neuropathic Pain

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Neuromodulation therapies.
Who it may be relevant to
Registry conditions: Neuropathic Pain. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Overview

The design and execution of the International Neuromodulation Society (INS) registry has been developed with the objective of assessing the efficacy and safety of Spinal Cord Stimulation and other neuromodulation therapies using real world data. The analysis of this registry as a data source will inform which therapies and devices are effective across clinics and participating countries. It is designed to combine data across multiple countries to enable research, benchmarking and device surveillance, and support for implant recalls. By combining longitudinal patient outcomes, device-level surveillance, and cross-center benchmarking, the registry will provide a powerful resource for evidence-based decision-making and international collaboration.

Interventions

  • Device Neuromodulation therapies
    Spinal cord stimulation (SCS) procedures

Primary outcome measures

  • Quality of life [Time frame: 12 Months]

Eligibility criteria

Inclusion criteria

  • Patients undergoing spinal cord stimulation (SCS) procedures
  • Obtain patient consent based on their local consent models

Exclusion criteria

  • Patient unable to meet study requirements

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07354243 · INR Registry

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗