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Targeted Disc Decompression (TDD) for Contained Herniated Lumbar Discs

NCT01429363 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 9

Last updated 2016-12-30

No results posted yet for this study

Summary

The prospective Clinical Series (CS) aims to prove the hypothesis that Targeted Disc Decompression (TDD) reduces the pain in patients suffering from radicular leg pain secondary to a contained focal disc protrusion (Lumboradicular Syndrome). Secondary objective will be to prove that the treatment Group will have less disability and better quality of life.

Conditions

  • Lumbar Spine Disc Herniation

Interventions

PROCEDURE

Targeted disc decompression

The Targeted disc catheter is connected to Neurotherm TDD unit and heating protocol is started.In this heating protocol temperature gradually increases from 65C to 90C during a time period of 12 minutes;

Sponsors & Collaborators

  • NeuroTherm

    collaborator UNKNOWN

  • Rijnstate Hospital

    lead OTHER

Principal Investigators

  • JW Kallewaard, Drs. · Rijnsate Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-08-31
Primary Completion
2016-12-31
Completion
2016-12-31

Countries

  • Netherlands

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 NCT01429363 on ClinicalTrials.gov