Spinal Cord stimulation (SCS) is a common intervention used in patients who suffer from chronic nerve pain following back surgery. This is known as failed back surgery syndrome (FBSS). Equally, the National Institute of Clinical Excellence (NICE) who work with the NHS, recommend suitable medicines and treatments for patients in their guidelines; suggest that SCS can be used in patients who have never had back surgery. The is no outcome data to define that SCS works in patients with neuropathic back pain, therefore this study will provide clinical data to see if this works. SCS delivers mild electrical impulses to the nerves along the spinal cord. This blocks the pain pathway from reaching the brain. This helps manage the pain experienced the lower back. A common side effect of the conventional system is that patients may experience 'pins and needles', tingling, and numbness, known as parathesia at site of stimulation. This can be particularly uncomfortable for patients. However, parathesia can be eliminated by changing certain settings on the stimulator. This could include increasing the frequency of the stimulator known as high frequency (HF). This works by delivering energy to site of stimulation below the parathesia threshold, so minimal or no parathesia is experienced. Only one study has been completed previously using HF frequency on patients with FBSS. The major findings from these studies have found that when compared to conventional SCS (uses a frequency of 40-80 Hz) that HF has provided better pain relief with minimal or no parathesia. Higher frequencies parameters are not completely novel because they have been used in patients who have FBSS. However, settings of 1000Hz which will be used in this study have not been done in patients who suffer from neuropathic pain and have not had any previous spinal surgery. Therefore, the main reason of this study is to investigate the response patients suffering from neuropathic pain and have not had previous spinal surgery, have to 1000Hz (HF) frequency spinal cord stimulation. We will also investigate the effect this setting has on the quality of life of the patients.
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Change from baseline numerical Rating Score (NRS) at 4 weeks
Timeframe: 4 weeks
change from baseline numerical Rating Score (NRS) at 3 months
Timeframe: 3 months
Change from baseline numerical Rating Score (NRS) at 6 months
Timeframe: 6 months
Change from baseline numerical Rating Score (NRS) at 12 months
Timeframe: 12 months
Change from baseline numerical Rating Score (NRS) at 24 months
Timeframe: 24 months
Change from baseline Oswestry Disability Index (ODI) scores at 4 weeks
Timeframe: 4 weeks
Change from baseline Oswestry Disability Index (ODI) scores at 3 months
Timeframe: 3 months
Change from baseline Oswestry Disability Index (ODI) scores at 6 months
Timeframe: 6 months
Change from baseline Oswestry Disability Index (ODI) scores at 12 months
Timeframe: 12 months
Change from baseline Oswestry Disability Index (ODI) scores at 24 months
Timeframe: 24 months
Change from baseline Patient's Global Impression of change (PGIC) scores to 4 weeks
Timeframe: 4 weeks
Change from baseline Patient's Global Impression of change (PGIC) scores to 3 months
Timeframe: 3 months
Change from baseline Patient's Global Impression of change (PGIC) scores to 6 months
Timeframe: 6 months
Change from baseline Patient's Global Impression of change (PGIC) scores to 12 months
Timeframe: 12 months
Change from baseline Patient's Global Impression of change (PGIC) scores to 24 months
Timeframe: 24 months
change from baseline EQ-5D-5L scores at 4 weeks
Timeframe: 4 weeks
change from baseline EQ-5D-5L scores at 3 months
Timeframe: 3 months.
change from baseline EQ-5D-5L scores at 6 months
Timeframe: 6 months.
change from baseline EQ-5D-5L scores at 12 months
Timeframe: 12 months.
change from baseline EQ-5D-5L scores at 24 months
Timeframe: 24 months.
Change from baseline Pain and Sleep 3 point index (PSQ-3) at 4 weeks
Timeframe: 4 weeks
Change from baseline Pain and Sleep 3 point index (PSQ-3) at 3 months
Timeframe: 3 months
Change from baseline Pain and Sleep 3 point index (PSQ-3) at 6 months
Timeframe: 6 months
Change from baseline Pain and Sleep 3 point index (PSQ-3) at 12 months
Timeframe: 12 months
Change from baseline Pain and Sleep 3 point index (PSQ-3) at 24 months
Timeframe: 24 months
Change from baseline Resource Questionnaire at 12 months
Timeframe: 12 months.
Change from baseline Resource Questionnaire at 24 months
Timeframe: 24 months.