An Implantable Spinal Cord Stimulation Pain Management System

Boston Scientific

Status and phase: Completed; Phase 3

Conditions: Back Pain; Pain, Intractable; Chronic Pain; Pain; Failed Back Surgery Syndrome

Treatments: Device: Precision SCS

Study type: Interventional

Funder types: Industry

Identifiers

NCT00205855

CR-S-003

Details and patient eligibility

About

There are many treatment options available for the management of chronic pain . Some include, but are not limited to, over-the-counter medications, Non-Steroidal Anti-Inflammatory Drugs, Physical Therapy, Transcutaneous Electrical Nerve Stimulation (TENS) and nerve blocks. Historically, the mainstay of pain treatment has been pharmacotherapy. However, pharmacotherapy has varying degrees of effectiveness and is often associated with undesirable side effects. Although many patients are successfully treated, for those who fail some of these more conservative therapies the remaining option is limited to spinal cord stimulation (SCS), proven to be an effective therapy to more than half of those failing conservative treatments . Over 50% of those who have failed these more conservative methods of pain management, can now, under the guidance of a clinician utilizing SCS, have their pain levels successfully managed. SCS is a less invasive therapy that is a reversible treatment with greater long-term benefits than more permanent, radical approaches and one that deserves greater consideration in the management of chronic, intractable pain.

Full description

This clinical trial was a confirmatory study for the Advanced Bionics totally implantable Spnial Cord Stimulation(SCS) System, the Stimulus System. This system is indicated as an aid in the management of chronic intractable pain of the trunk and/or limbs, including unilateral or bilateral pain associated with the following: Dailed back surgery syndrome, intractable low backpain and leg pain.

Enrollment: 65 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Diagnosed with chronic, intractable pain of the trunk and/or limbs which includes but is not limited to, unilateral or bilateral pain associated with any of the following: failed back surgery syndrome, intractable low back pain and leg pain.
2. Be an appropriate candidate for surgery.
3. Be capable of giving informed consent.
4. Be capable and willing to follow all study related procedures.

Exclusion criteria

1. Have an inability to operate the system either by self or care-giver.
2. Are currently participating or have participated within the past 30 days in any clinical investigation that could conflict with the requirements of this study.
3. Have any implanted electrical devices, regardless of whether active or inactive.
4. Have any active implantable device regardless of whether stimulation is ON or OFF.

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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65 participants in 1 patient group

Precision SCS

Experimental group

Description:

Precision SCS. Patients who receive Precision Spinal Cord Stimulator (SCS) Stimulus system

Treatment:

Device: Precision SCS