Neuromodulation Parameter Efficacy

Alberta Health Services, Calgary

Status: Enrolling

Conditions: Chronic Pain

Treatments: Other: Stimulation parameters

Study type: Interventional

Funder types: Other

Identifiers

NCT04933370

REB21-0692

Details and patient eligibility

About

The objective of this study is to determine the efficacy of neuromodulation using various stimulation paradigms in the treatment of several disorders including chronic pain.

Full description

Different stimulation parameters will be tried in a blinded fashion to compare efficacy.

Enrollment: 20 estimated patients

Sex: All

Ages: 18 to 100 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Patients who are candidates for, and have been consented for, implantation of a neuromodulation device.

Exclusion criteria

• Non-English speaking

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Quadruple Blind

---

20 participants in 2 patient groups

Industry standard stimulation

Active Comparator group

Description:

Industry standard stimulation settings

Treatment:

Other: Stimulation parameters

Experimental stimulation

Sham Comparator group

Description:

Experimental stimulation settings

Treatment:

Other: Stimulation parameters