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Predicting Outcome of Transcutaneous Electrical Nerve Stimulator (TENS) in Failed Back Surgery Syndrome

NCT01185665 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2010-08-20

No results posted yet for this study

Summary

The study investigates the feasibility and efficacy of Transcutaneous Electrical Nerve Stimulator (TENS) in a subgroup of patients with neuropathic pain. Those patients are suffering of neuropathic pain at the lower back and leg after spinal surgery with a predominance of pain in the leg.

Conditions

  • Failed Back Surgery Syndrome

Interventions

DEVICE

TENS

Transcutaneous Electrical Nerve Stimulator

DEVICE

Sham-TENS

TENS without electrical output, from the outside not different from a normal TENS

Sponsors & Collaborators

  • Evenepoel Kristof

    collaborator UNKNOWN

  • De Rudder Marc

    collaborator UNKNOWN

  • Dokter Moens Maarten (primary investigator)

    collaborator UNKNOWN

  • Prof. dr. Cattrysse Eric

    collaborator UNKNOWN

  • Prof. Dr. D'Haens Jean

    collaborator UNKNOWN

  • Universitair Ziekenhuis Brussel

    lead OTHER

Principal Investigators

  • Maarten Moens, M.D. · Universitair Ziekenhuis Brussel

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-09-30
Primary Completion
2011-09-30
Completion
2011-09-30

Countries

  • Belgium

Study Locations

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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 NCT01185665 on ClinicalTrials.gov