Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
RECRUITING
NCT05861609
NA

Pain Medication Tapering for Patients With Persistent Spinal Pain Syndrome Type 2, Treated With Spinal Cord Stimulation.

Sponsor: Moens Maarten

View on ClinicalTrials.gov

Summary

The primary objective of the study is to examine whether there is a difference in disability after 12 months of Spinal Cord Stimulation (SCS) in patients with Persistent Spinal Pain Syndrome Type 2 (PSPS T2) after receiving a standardized pain medication tapering protocol before SCS implantation, a personalized pain medication tapering protocol before SCS implantation, or no tapering protocol before SCS implantation. The secondary objective of the study is to examine whether there is a difference after 12 months of SCS in PSPS T2 patients after receiving a standardized pain medication tapering protocol before SCS implantation, a personalized pain medication tapering protocol before SCS implantation, or no tapering protocol before SCS implantation on pain intensity, health-related quality of life, participation, domains affected by substance use, anxiety and depression, medication use, psychological constructs, sleep, central sensitization, and healthcare expenditure.

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

195

Start Date

2023-09-29

Completion Date

2026-09

Last Updated

2023-10-18

Healthy Volunteers

No

Interventions

PROCEDURE

Usual care

Usual care with respect to Spinal Cord Stimulation implantation

PROCEDURE

Standardized pain medication tapering

A standardized pain medication tapering program before Spinal Cord Stimulator implantation.

PROCEDURE

Personalized pain medication tapering

A personalized pain medication tapering program before Spinal Cord Stimulator implantation.

Locations (3)

Universitair Ziekenhuis Brussel

Jette, Belgium

Heilig Hart Ziekenhuis Lier

Lier, Belgium

AZ Delta

Roeselare, Belgium