Clinical Trials Logo

Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT04020211
Other study ID # CA2018-5 US CPSP-3
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date March 14, 2019
Est. completion date December 12, 2019

Study information

Verified date November 2020
Source Nevro Corp
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This is a multi-center study where patients who meet the eligibility criteria will be treated with HF10 therapy for their chronic knee pain post-orthopedic surgery. The primary endpoint will be assessed at 3 months, but observational assessments will continue until study completion at 12 months following implant.


Recruitment information / eligibility

Status Terminated
Enrollment 3
Est. completion date December 12, 2019
Est. primary completion date December 12, 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Key Inclusion Criteria: 1. Have been diagnosed with chronic, focal, neuropathic pain following orthopedic surgery(ies) of the knee(s). 2. Average pain intensity (over a period of 7 days) of =5 out 10 cm on the Visual Analog Scale (VAS) in the primary area of pain at enrollment. 3. Have a score of at least 4 out of 10 in Douleur Neuropathique 4 (DN4) questionnaire at the time of enrollment or eligibility verification. 4. Deemed not to have surgical loosening or other complications from the surgery that affect the stability of the knee. 5. Have stable neurological status measured by motor, sensory and reflex function as determined by the investigator. 6. Be on stable pain medications, as determined by the Investigator, for at least 28 days prior to assessing pain intensity as described in inclusion criterion #2, and be willing to stay on those medications with no dose adjustments until activation of the permanently implanted SCS device. Key Exclusion Criteria: 1. Have radiculopathy or radicular leg pain resulting from failed back surgery. 2. Have a medical condition or pain in other area(s), not intended to be treated with SCS, that could interfere with study procedures, accurate pain reporting, and/or confound evaluation of study endpoints, as determined by the Investigator (such as primary headache diagnosis or fibromyalgia). 3. Have a current diagnosis of a progressive neurological disease such as multiple sclerosis (MS), chronic inflammatory demyelinating polyneuropathy, rapidly progressive arachnoiditis, brain or spinal cord tumor, central deafferentation syndrome, acute herniating disc, severe spinal stenosis and brachial plexus avulsion as determined by the Investigator. 4. Have a current diagnosis or condition such as a coagulation disorder, bleeding diathesis, platelet dysfunction, progressive peripheral vascular disease or uncontrolled diabetes mellitus that presents excess risk for performing the procedure as determined clinically by the Investigator. 5. Have any prior experience with SCS. 6. Have objective evidence of epidural scarring and/or any signs or symptoms of myelopathy as determined by the investigator. 7. Be benefitting from an interventional procedure to treat their trunk or limb pain (Subjects should be enrolled at least 30 days from last benefit). 8. Have an existing drug pump and/or another active implantable device such as a pacemaker. 9. Be involved in an injury claim under current litigation. 10. Have an active or unsettled worker's compensation claim.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Senza HF10 Therapy
Senza 10kHz Spinal Cord Stimulation

Locations

Country Name City State
United States Pain Management Greenfield Wisconsin

Sponsors (1)

Lead Sponsor Collaborator
Nevro Corp

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Responders and Improvement in Oxford Knee Score (OKS) The OKS is a patient self-completion patient reported outcome containing 12 questions on activities of daily living with a recall period of 4 weeks. The OKS has been developed and validated specifically to assess function and pain after total knee replacement. The higher the score indicates improvement. The proportion of implanted subjects who are responders (achieved = 50% pain relief) to HF10 therapy for treatment of their chronic, post-surgical knee pain or reporting at least a 4-point improvement in their Oxford Knee Score (OKS). 3 months
Secondary Change in Disability and Functioning Percentage and average change from Baseline in Oxford Knee Score 3, 6, and 12 months
Secondary Change in Functioning Average change in walking distance assessed by 6-minute Walk Test 3 and 12 months
Secondary Change in Functioning Change in Global Assessment of Functioning 3 and 12 months
Secondary Change in pain relief as measured by the Visual Analog Scale (VAS) Percentage and average change from Baseline in knee pain intensity 3 and 12 months
Secondary Change from baseline in pain experience: Short-Form McGill Pain Questionnaire (SF-MPQ-2) scores The Short Form McGill Pain Questionnaire version 2 (SF-MPQ-2, hereafter referred to as MPQ) is a well validated and widely used questionnaire used to measure the major symptoms of pain. Subjects will be asked to rate the intensity of each of 22 pain descriptors from 0 (do not experience, or none) to 10 (worst possible) at follow-up visits outlined in the schedule of events.
Four subscale scores (continuous pain, intermittent pain, predominantly neuropathic pain, and affective descriptors) and a total score will be calculated. The lower the score indicates improvement (less interference from pain). Each subject's baseline scores will be compared to the scores at study visits. Mean change from baseline will be calculated for the entire cohort.
Percentage and average change from Baseline in Short-Form McGill Pain Questionnaire (SF-MPQ-2) scores
3 and 12 months
Secondary Global Impression of Change Subject's impression of change in overall health condition as measured by the Patient and Clinician Global Impression of Change 3 and 12 months
Secondary Change in Quality of Life as measured by the EuroQol five-dimensional questionnaire (EQ-5D-5L) The 5-level EQ-5D version (EQ-5D-5L) uses a 2-part assessment: a descriptive one and a visual analog scale. The descriptive system comprises five dimensions: mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 5 levels: no problems, slight problems, moderate problems, severe problems and extreme problems. The patient is asked to indicate his/her health state by ticking the box next to the most appropriate statement in each of the five dimensions. This decision results in a 1-digit number that expresses the level selected for that dimension. The digits for the five dimensions can be combined into a 5-digit number that describes the patient's health state. The higher the score indicates an improved in quality of life. Change from Baseline in health-related quality of life evaluation 3 and 12 months
Secondary Change in Sleep as measured by the Pain and sleep Questionnaire (PSQ) PSQ is an eight-item questionnaire developed to assess the impact of pain on sleep. PSQ-3 is a subset of PSQ, consisting of questions 1, 4 and 5 and has been validated to assess impact of chronic pain on sleep. The lower the score indicates improvement by less interference of sleep from pain. Change from baseline in 3-item pain and sleep questionnaire 3 and 12 months
Secondary Medication Change from baseline in opioid equivalent medication usage 3 and 12 months
Secondary Safety profile: Incidence of AEs over time Incidence of AEs over time 3, 6 and 12 months
Secondary Safety profile: Neurological assessment over time by a physician and exam Neurologic status includes testing for gross motor, sensory and appropriate reflex functions, which will be characterized as improved, maintained, or a deficit as compared with baseline status as follows: A clinically meaningful neurological improvement is defined as a significant persistent improvement in neurological function that impacts subject's well-being is attributable to a neurological finding; and is new or improved as compared with the baseline assessment. A clinically meaningful neurological deficit is defined as a stimulation-related significant persistent abnormality in neurological function that impacts subject's well-being is attributable to a neurological finding; and is new or worsened as compared with the baseline assessment. If neither a clinically meaningful neurological improvement nor a clinically meaningful neurological deficit is observed, then neurologic status is maintained. 3, 6 and 12 months
See also
  Status Clinical Trial Phase
Completed NCT04138329 - Comparison of Postoperative Inguinal Pain Between the Onstep Technique and the Lichtenstein Technique N/A
Recruiting NCT04209868 - Preoperative Paravertebral Block in Cancer Surgery of the Lung Phase 2/Phase 3
Completed NCT03448913 - Block REducing Pain After Surgery Trial
Completed NCT03119896 - Supporting Self-management of Chronic Pain N/A
Completed NCT03986866 - Video-based, Patient-Focused Opioid Education in the Perioperative Period N/A
Completed NCT03451695 - Effect of Intrathecal Morphine on Chronic Pain After Elective Caesarean Section Phase 4