Spinal Cord Stimulation for Refractory Pain Randomized Controlled Trial: the PAcStim RCT

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Health Network, Toronto

About this trial

Neuropathic pain affects 6-10% of the global population and is poorly managed - current drug treatments succeed in only \~25% of patients. Spinal cord stimulation (SCS) modulates pain by electrically stimulating spinal dorsal column fibres. The newer paresthesia-free mode (PF-SCS, 500-10,000 Hz) appears more effective and tolerable than traditional paresthesia-based SCS, with superior outcomes shown in the SENZA-RCT. All promising PF-SCS studies have been unblinded, making them susceptible to placebo effects. The one blinded RCT that exists had significant methodological flaws (no washout period, single baseline measurement) that biased results toward the null. A blinded, multi-centre, crossover RCT in 90 patients comparing 6 weeks of active PF-SCS vs. 6 weeks of placebo stimulation, with a 2-week washout in between - designed to correct the flaws of the prior trial and definitively establish whether PF-SCS works beyond placebo.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 18 years or older

Severe NP in the axial locations (neck and back) and/ or the limbs

Undergoing an SCS implantation with a PF device

Disqualifiers

Previously implanted with an SCS device

Not fluent in English

Unable to provide written informed consent

Trial design

Design model

Crossover

Treatments tested in this trial

  • Paresthesia-free spinal cord stimulation

    Device

    At the beginning of the PF-SCS phase, the unblinded trial nurse will set the stimulator to provide active stimulation \[500-1200 Hz at 70% of the perception amplitude - usually between 3 to 5 mA\], which will remain constant for the 6-week duration of this period.

Treatment groups

90 Participants
are divided into 2 treatment groups
Group A: paresthesia-free spinal cord stimulation (PF-SCS)Experimental treatment 1 intervention
Group B: PlaceboPlacebo comparator 1 intervention

Trial outcomes

Primary outcomes

1

Evaluate the analgesic outcomes from PF-SCS against outcomes from placebo

PAcStim will compare the effect of 6 weeks of treatment with PF-SCS and placebo on Pain intensity, measured using the 0 to 10 pain numeric rating scale

Time frame
14-week

Secondary outcomes

1

Evaluate the impact of PF-SCS on daily activity and sleep duration

The secondary goals are to evaluate the impact of PF-SCS on daily activity and sleep duration using wearable actigraphy monitors

Time frame
14-week

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: