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Focal Pain Outcomes Using Configurations Applied for Lateral Stimulation

NCT04073446 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 3

Last updated 2023-03-29

Study results available
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Summary

To evaluate programming modalities at various targets for focal foot, knee pain, and groin pain relief.

Conditions

Interventions

DEVICE

Spinal Cord Stimulation

Patients eligible for SCS

Sponsors & Collaborators

  • Boston Scientific Corporation

    lead INDUSTRY

Principal Investigators

  • Roshini Jain · Boston Scientific Corporation

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-10-31
Primary Completion
2021-10-01
Completion
2021-10-01
FDA Device
Yes

Countries

  • Belgium

Study Locations

More Related Trials

Entities

Diseases

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 NCT04073446 on ClinicalTrials.gov