Automatic Control of Spinal Cord Stimulatio

Not Applicable

Recruiting

• Conditions: Chronic Pain; Anaesthesiology - Pain management

• Registration Number: ACTRN12611001263987
• Lead Sponsor: ational ICT Australia Ltd

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2011-12-09
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 25

Inclusion Criteria

Patients implanted with a commercially available electrode lead who are part of a routine clinical trial stimulation program prior to possible permanent implant.
Patients are capable of fulfilling the requirements of this protocol including reporting of patient percepts.

Exclusion Criteria

Patients implanted with a commercially available electrode lead who have had complications such that the implanted electrodes are not able to stimulate and record over the spinal cord.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Patient verbal rating of the percentage of stimulation coverage of total pain areas and recorded in a computer questionnaire spreadsheet[Measured at different postures and with different stimulation types in one experimental session];Patient verbal rating of stimulation strength from 0 to 10 (nothing to maximum possible strength) and recorded in a computer questionnaire spreadsheet[Measured at different postures and with different stimulation types in one experimental session]

Secondary Outcome Measures

Name	Time	Method
Patient verbal rating of pain relief on a Numerical Rating Scale of 0-10 (no pain to maximum possible pain) and recorded in a computer questionnaire spreadsheet[Measured with different stimulation types in one experimental session]