Remote Programming in Spinal Cord and Dorsal Root Ganglion Stimulation

Remote Programming in Spinal Cord and Dorsal Root Ganglion Stimulation - Remote SCS

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00028278

Enrollment

Registered

2022-02-28

Start date

2022-04-01

Completion date

Unknown

Last updated

2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

R52.1

Interventions

Group 1: Retrospective arm - Retrospective data collection of the previously in-person programmed outpatients under spinal cord and dorsal root ganglion stimulation. Group 2: Prospective arm - Prospec

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Implantation of a definitive system for spinal cord stimulation or dorsal root ganglion stimulation. 2. Pain intensity of more than 5 on visual analog scale for more than 3 months. 3. The patient has the ability to read, understand and give information reliably as required by the protocol.

Exclusion criteria

Exclusion criteria: 1. Patients with another pain disorder, which could influence the study results 2. Adults unable to give consent 3. Children and adolescents

Design outcomes

Primary

Measure	Time frame
Pain intensity in the visual analog scale (VAS) on days 30, 60 and 90 after implantation	—

Secondary

Measure	Time frame
Coverage of the painful area, analgesics intake, travel costs, travel time, patient satisfaction	—

Countries

Germany

Contacts

Public ContactGuilherme Santos Piedade

Universitätsklinikum Düsseldorf

guilherme.santospiedade@med.uni-duesseldorf.de0211 81 16058

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026