Focal Pain Outcomes Using Configurations Applied for Lateral Stimulation
CompletedNot applicableNCT04073446
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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)
To evaluate programming modalities at various targets for focal foot, knee pain, and groin pain relief.
Study details
- Official title
- Focal Pain Outcomes Using Configurations Applied for Lateral Stimulation
- Conditions
- Interventions
- Sponsor
- Boston Scientific Corporation
- Start date
- 2019-10-31
- Primary completion
- 2021-10-01
- Sex
- All
- Age range
- from 18 Years
- Results posted
- Yes, on ClinicalTrials.gov
- Countries
- Belgium
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Key Inclusion Criteria: * Average unilateral foot, or knee or groin pain intensity of 6 or greater on a 0-10 numerical rating scale at Baseline Visit based on 7-day average NRS score * Subject signed a valid, EC-approved informed consent form (ICF) * Willing and able to comply with all protocol-required procedures and assessments/evaluations * 18 years of age or older when written informed consent is obtained Key Exclusion Criteria: * Significant cognitive impairment at Screening that, in the opinion of the Investigator, would reasonably be expected to impair the study candidates to participate in the study * Participating (or intends to participate) in another drug or device clinical trial that may influence the data that will be collected for this study
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT04073446