NCT02896361View on ClinicalTrials.gov

Burst Optimized Stimulation Study

NACompletedINTERVENTIONAL
Enrollment

29

Participants

Timeline

Start Date

July 31, 2016

Primary Completion Date

August 31, 2017

Study Completion Date

August 31, 2017

Conditions
Chronic Pain
Interventions
DEVICE

Reprogramming of spinal cord stimulator (Proclaim or Prodigy SJM internal pulse generator) parameters according to study protocol

Stimulation parameters are reprogrammed from original values to study defined ones

Trial Locations (3)

2610

NKO Sint-Augustinus, Antwerp

40225

Medizinische Einrichtungen der Universität Düsseldorf, Düsseldorf

47055

Klinikum Duisburg GmbH, Duisburg

Sponsors
All Listed Sponsors
collaborator

Medizinische Einrichtungen der Universität Düsseldorf

UNKNOWN

collaborator

Klinikum Duisburg GmbH

UNKNOWN

collaborator

NKO Sint-Augustinus Antwerpen

UNKNOWN

lead

Abbott Medical Devices

INDUSTRY