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A Prospective Trial for the Effectiveness of the Use of Spinal Cord Stimulation (SCS) in Failed Knee Surgery

NCT01912924 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2013-07-31

No results posted yet for this study

Summary

A study for patients who have chronic postoperative pain who had knee replacement surgery. If qualified, a 14 day trial and an implantation of spinal cord stimulator for control of pain will be administered. This study will evaluate effectiveness of pain control. Subjects will be followed for one year post implantation.

Conditions

Interventions

DEVICE

Spinal cord stimulator (Boston Scientific)

spinal cord stimulator trial leads and hand held battery

Sponsors & Collaborators

  • Boston Scientific Corporation

    collaborator INDUSTRY

  • Coastal Orthopedics & Sports Medicine

    lead OTHER

Principal Investigators

  • Gennady Gekht, MD · Coastal Orthopedics & Sports Medicine

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-08-31
Primary Completion
2013-05-31
Completion
2013-05-31

Countries

  • United States

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 NCT01912924 on ClinicalTrials.gov