Efficacy Study of the Octapolar Lead in Patients With Failed Back Surgery Syndrome (FBSS) With Chronic Pain
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|ClinicalTrials.gov Identifier: NCT01096147|
Recruitment Status : Completed
First Posted : March 30, 2010
Last Update Posted : November 4, 2013
Spinal cord stimulation (SCS) has been used for over 40 years to treat neuropathic pain. Various clinical studies have shown a beneficial effect of SCS on pain in patients with Failed Back Surgery Syndrome (FBSS). Since more than 2 years the 8-contact points Octad lead has been used and replaced the 4-contact points Quad lead. Even though it seems that eight electrodes has potential advantage over the four electrodes in case of lead migration or disease progress, no clinical data have been published on the effectiveness of SCS using the octopolar epidural lead. The Octad study intents to assess the effectiveness and technical performance of SCS with the Octad® lead for treatment of chronic pain. This study is not set up as a comparison study between the Octad lead and other SCS leads, such as the Quad lead, because the Octad lead is used in most eligible FBSS patients as the standard of care lead.
The study intends to:
- evaluate the effectiveness of SCS with the Octad® lead on chronic pain in Failed Back Surgery Syndrome patients after 12 months of treatment.
- collect safety data for SCS with the Octad® lead in patients with refractory chronic pain.
|Condition or disease||Intervention/treatment||Phase|
|Failed Back Surgery Syndrome||Device: Spinal cord stimulation with eight polar electrode||Phase 4|
The use of Spinal Cord Stimulation (SCS) for pain control has already a history of more than 40 years. In SCS, a lead is positioned in the epidural space on the dorsal aspect of the spinal cord so as to produce stimulation induced paraesthesia in the painful area. During the last decades many articles have been published, clearly indicating the effectiveness and safety of SCS with quadripolar leads in the pain management of chronic neuropathic pain, and in particular Failed Back Surgery Syndrome (FBSS). Randomized controlled trials demonstrated that compared with re-operation, SCS provides effective pain relief for at least 3 years and compared with conventional non-surgical neuropathic pain management for at least 2 years.
However, SCS-related complications can occur, that can be divided into surgical complications and hardware complications. The hardware technology has substantially improved over the years. Moreover, electrodes have become smaller in shape and easier to navigate through the epidural space; and finally, internal pulse generators have new programming capabilities and a longer battery life span. All these technological developments led to the application of minimally invasive percutaneous stimulation trials for a variety of patients with chronic neuropathic pain. Turner et al performed a meta-analysis of spinal cord stimulation for failed back surgery syndrome publications and reported hardware complications of 24% lead migration, 7% lead failure and 2% pulse generator failure. While this analysis evaluated studies using older hardware systems, there is first evidence that the rate of these complications is lower currently with new systems. In the recently published PROCESS paper, also using quadripolar electrodes, long term follow-up showed that hardware complications were 14%: lead migration, 3% lead failure and no pulse generator failures.
Generally, patients with radicular pain to the lower extremities respond better to spinal cord stimulation than patients with isolated axial low back pain. However, a few studies have shown that axial low back pain in combination with bilateral leg pain, also respond well to spinal cord stimulation. Both four (e.g. quadripolar Quad lead) and eight (e.g. octapolar Octad® lead) electrodes were shown to be effective in treatment of low back and lower extremity pain, with no apparent advantage of one system over the other. In the recent PROCESS study publication, the reduction of SCS on low-back pain was not-statistically significant when compared to baseline. Even though it seems that eight electrodes may have the potential advantage in case of lead migration or disease progress, no clinical data have been published on the effectiveness of SCS using the octopolar epidural lead. The Octad study is a prospective, multi-center, open-label, non-randomized, interventional study designed to assess the effectiveness and technical performance of SCS with the Octad® lead for treatment of chronic pain. This study is not set up as a comparison study between the Octad lead and other SCS leads, such as the Quad lead, because the Octad lead is used in most eligible FBSS patients as the standard of care lead.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||80 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Octad Study: Evaluation of the Effectiveness of the Octopolar Lead in Patients With Failed Back Surgery Syndrome With Low Back and/or Leg Pain During a One Year Follow-up Period|
|Study Start Date :||February 2010|
|Actual Primary Completion Date :||March 2013|
|Actual Study Completion Date :||November 2013|
Active Comparator: SCS
patients receiving SCS for chronic leg and/or back pain.
Device: Spinal cord stimulation with eight polar electrode
In SCS a lead is positioned in the epidural space on the dorsal aspect of the spinal cord as to produce electrically induced paraesthesia in the painful area.
Other Name: Spinal column stimulation
- Pain suppression in low back and/or leg [ Time Frame: 12 months ]Evaluate the evolution of pain control with the octopolar Octad® lead assessed by a decrease in VAS for leg (and low-back pain separately, if applicable) during 12 months follow-up. Actual pain, the least pain during the last week and the worst pain during the last week are scored.
- adverse events related to SCS [ Time Frame: 12 months ]Clinical (such as surgery related infections) and technical (such as lead fractures) adverse events will be collected continuously in all patients during a period of 12 months post implant.
- quality of life [ Time Frame: 12 months ]Quality of life assessed by EuroQol group - 5 Dimensions (EQ-5D)
- sleep [ Time Frame: 12 months ]Sleep is assessed by a 3 item questionnaire on sleep quality, falling asleep and waking up from pain.
- pain medication intake [ Time Frame: 12 months ]Data will be collected at specific times on health service resourse use of concomitant pain medication such as opioids.
- Healthcare resource utilization [ Time Frame: 12 months ]Data will be collected at specific times on health service resourse use of concomitant non-drug therapy use, such as physiotherapy, related to FBSS.
- preferred stimulation settings [ Time Frame: 12 months ]Characterization of pulsegenerator parameters, such as amplitude, pulse width, stimulation frequency, electrode configuration (positive and negative poles), number of stimulation programs, and stimulation duration is done at specific times.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01096147
|Hospital ZNA Middelheim|
|Antwerpen, Belgium, 2020|
|Hospital St Jan|
|Brugge, Belgium, 8000|
|Hospital Alma Eeklo|
|Eeklo, Belgium, 9900|
|University Hospital Gent|
|Gent, Belgium, 9000|
|Sint-Niklaas, Belgium, 9100|
|Zottegem, Belgium, 9620|
|Stavanger University Hospital|
|Stavanger, Norway, 4068|
|Gothenburg, Sweden, 41345|
|Principal Investigator:||Ann Ver Donck, MD PhD||Hospital St Jan, Brugge, Belgium|
|Principal Investigator:||Kliment P Gatzinsky, MD PhD||Sahlgrenska University Hospital, Gothenburg, Sweden|
|Principal Investigator:||Roald Baardsen, MD PhD||University hospital Stavanger, Stavanger, Norway|