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SCS System
FAST Spinal Cord Stimulation for Chronic Pain (FAST Trial)
N/A
Waitlist Available
Research Sponsored by Boston Scientific Corporation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Key
Chronic pain (predominantly neuropathic) of the trunk and/or limbs for at least 6 months with back pain greater or equal to leg pain.
Must not have
Breast-feeding or planning to get pregnant during the course of the study or not using adequate contraception
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 months post-activation
Awards & highlights
No Placebo-Only Group
Summary
This trial is testing a new pain relief treatment that acts quickly and doesn't cause tingling. It targets patients with chronic pain who don't respond well to regular treatments. The treatment uses a device that sends electrical signals to the spine to block pain.
Who is the study for?
This trial is for adults over 22 with chronic pain, specifically neuropathic pain in the trunk or limbs that's lasted at least 6 months. Participants must be able to read and understand English, complete questionnaires, and have signed an informed consent form. It excludes those with conditions that could affect study results, significant cognitive impairments, pregnant or breastfeeding individuals not using contraception, or anyone in another conflicting clinical trial.
What is being tested?
The effectiveness of a new therapy called FAST-SCS (fast-acting paresthesia-free) is being tested using the Boston Scientific WaveWriter SCS System on patients with chronic pain. The study will also look into additional SCS therapy options provided by this system.
What are the potential side effects?
While specific side effects are not listed here, typical side effects from similar spinal cord stimulation systems can include discomfort at the implant site, tingling sensations due to electrical pulses (paresthesia), infection risk from surgery, and potential equipment malfunction.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
It seems like the criterion is incomplete. Could you provide more details or context so I can assist you better?
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I have had chronic pain in my back or limbs for at least 6 months, with back pain being the most severe.
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I am 22 years old or older.
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I have had chronic pain in my back or limbs for at least 6 months, with back pain being as bad or worse than leg pain.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I am not breastfeeding, planning to become pregnant, or not using birth control.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3 months post-activation
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 months post-activation
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Targeted Pain Responder Rate
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: WaveWriter SettingsExperimental Treatment1 Intervention
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Spinal Cord Stimulation (SCS) works by delivering electrical impulses to the spinal cord to modulate pain signals before they reach the brain, effectively inhibiting pain transmission and activating inhibitory pathways. The FAST-SCS, a newer approach, aims to provide pain relief without the tingling sensation (paresthesia) associated with traditional SCS.
This is significant for chronic pain patients as it offers a more comfortable and potentially more effective pain management option, enhancing their quality of life without the discomfort of paresthesia.
Italian multicentric study on pain treatment with epidural spinal cord stimulation.Spinal Cord Stimulation for Neuropathic Pain: Current Trends and Future Applications.Spinal cord stimulation modulates descending pain inhibition and temporal summation of pricking pain in patients with neuropathic pain.
Italian multicentric study on pain treatment with epidural spinal cord stimulation.Spinal Cord Stimulation for Neuropathic Pain: Current Trends and Future Applications.Spinal cord stimulation modulates descending pain inhibition and temporal summation of pricking pain in patients with neuropathic pain.
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Who is running the clinical trial?
Boston Scientific CorporationLead Sponsor
742 Previous Clinical Trials
857,265 Total Patients Enrolled
32 Trials studying Chronic Pain
63,790 Patients Enrolled for Chronic Pain
Natalie Bloom LyonsStudy DirectorBoston Scientific Corporation
15 Previous Clinical Trials
24,595 Total Patients Enrolled
4 Trials studying Chronic Pain
10,306 Patients Enrolled for Chronic Pain
Roshini JainStudy DirectorBoston Scientific Corporation
30 Previous Clinical Trials
26,122 Total Patients Enrolled
12 Trials studying Chronic Pain
11,331 Patients Enrolled for Chronic Pain
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am not breastfeeding, planning to become pregnant, or not using birth control.You have any medical or psychological conditions that could make it difficult to accurately report how you are feeling during the study.It seems like the criterion is incomplete. Could you provide more details or context so I can assist you better?I have had chronic pain in my back or limbs for at least 6 months, with back pain being the most severe.I am 22 years old or older.I have had chronic pain in my back or limbs for at least 6 months, with back pain being as bad or worse than leg pain.I have signed an informed consent form in English.
Research Study Groups:
This trial has the following groups:- Group 1: WaveWriter Settings
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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