Clinical Trial of the Senza™ SCS System in the Treatment of Chronic Upper Limb and Neck Pain

NCT02385201 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2018-10-09

No results posted yet for this study

Summary

This is a prospective, multi-center feasibility study of effectiveness and safety of the Senza System in subjects with chronic, intractable pain of the upper limbs and/or neck. Data at follow-up visits will be compared to Baseline data collected at the beginning of the study.

Conditions

Interventions

DEVICE

Senza

Spinal Cord Stimulation

Sponsors & Collaborators

  • Nevro Corp

    lead INDUSTRY

Principal Investigators

  • Brad Gliner · Nevro Corp

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-30
Primary Completion
2017-06-30
Completion
2018-03-31

Countries

  • United States

Study Locations

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Entities

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 NCT02385201 on ClinicalTrials.gov