Evaluate the Safety and Efficacy of a Peripheral Nerve Stimulation

Shanghai Jiao Tong University

Status

Enrolling

Conditions

Complications; Prosthesis, Nervous System, Peripheral, Pain

Treatments

Device: Percutaneous peripheral nerve stimulation system

Study type

Interventional

Funder types

Other

Identifiers

NCT05827848

XH-22-007

Details and patient eligibility

About

This trial was conducted in a prospective, multicenter, randomized withdrawal design at a designated clinical trial facility. The total sample size for this trial is expected to be 59-62 patients.

One to two subjects were conducted in each study center as a preliminary test. A total of about 3-6 subjects were selected for the pre-test. The pre-test subjects used the test equipment (on state) and were not randomized.

The study was divided into screening/baseline period, treatment period (including test period, random withdrawal period and observation period) and follow-up period.

All subjects underwent a 7-day baseline assessment (VAS score for at least 4 days) during the screening/baseline period. Eligible subjects underwent Peripheral Nerve Stimulation(PNS) surgery and implanted electrode leads and entered the 7-day test period. During the test period, subjects with an average VAS score improvement of ≥30%(VAS score for at least 4 days) will be randomly assigned to the experimental group (on state) or the control group (off state) in a 1:1 ratio for 7 days observation. All subjects were enrolled in the observation period until 28 days after implantation. Safety assessment was performed at a 14-day follow-up after removal of the device.

Enrollment

62 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age ≥18 years old, gender unlimited;
The investigator judged that there was definite peripheral neuropathic pain (chronic and refractory pain in the trunk and extremities, including chronic pain after sternal surgery; Postherpetic neuralgia), suitable for percutaneous peripheral nerve stimulation system treatment;
Preoperative assessment by neuropathic Pain Scale (DN4) showed that there were related damages or diseases in the peripheral sensory system;
Patients with poor efficacy or can not tolerate the side effects of treatment after routine treatment;
Visual analogue scale (VAS)≥50mm within 24 hours before treatment;
The subject can understand the study purpose, demonstrate sufficient compliance with the study protocol, and be able and willing to sign the informed consent.

Exclusion criteria

Patients who need to be treated with radiofrequency regulation and intrathecal drug infusion;
Patients who are known to have had heart implants (pacemakers or defibrillators) or other implanted neurostimulators (spinal cord stimulators or deep brain stimulators, etc.);
Patients with severe psychological and/or psychiatric illness and/or non-therapeutic drug dependence;
Patients who are expected to undergo MRI within 30 days after PNS implantation;
Expected to be discharged within 48 hours or less;
There is known damage to the target nerve or muscle defect in the pain area;
Patients with known allergies to skin-to-skin contact materials (tape or adhesive);
Known allergy to anesthetics such as lidocaine;
Preoperative complications of severe heart, liver, kidney, respiratory diseases and coagulopathy;
Pregnant or lactating women, or have a birth plan in the next 3 months;
Is participating in any other drug or medical device clinical trial, or may participate in any other drug or medical device clinical trial after enrollment in this clinical trial;
The investigator determined that there were other conditions that were not suitable to participate in the clinical trial.