Ultrasound-guided Sacroiliac Joint Radiofrequency Ablation: A Pilot Study

NACompletedINTERVENTIONAL
Enrollment

31

Participants

Timeline

Start Date

September 30, 2015

Primary Completion Date

July 31, 2018

Study Completion Date

July 31, 2018

Conditions
Sprain of Sacroiliac LigamentLow Back PainOsteoarthritis Nos, of Sacroiliac Joint
Interventions
PROCEDURE

Radiofrequency ablation

RF ablation will be performed using 2 Nimbus multitined electrodes in a bipolar configuration. The electrodes will be placed along the lateral crest using a leap-frogging technique from the inferomedial aspect of the PSIS to the third transverse sacral tubercle at 1.5-2 cm intervals at the skin surface. A radiofrequency current will be passed for 120 seconds per site resulting in thermal coagulation of the plexus. Prior to performing the thermal lesion, electrical stimulation at 2 Hz and 2.0 V will be administered.

PROCEDURE

Sensory block

Participants will undergo a lidocaine block of the PSN at the lateral crest under ultrasound guidance. 0.5 mL of 2% lidocaine will be injected from the inferomedial border of the PSIS to the third transverse sacral tubercle at approximately 1.5 cm intervals along the skin surface.

DRUG

Lidocaine

Trial Locations (1)

N6A4V2

St. Joseph's Pain Clinic, London

All Listed Sponsors
collaborator

University of Toronto

OTHER

collaborator

University of Alberta

OTHER

lead

Western University, Canada

OTHER

NCT02335190 - Ultrasound-guided Sacroiliac Joint Radiofrequency Ablation: A Pilot Study | Biotech Hunter | Biotech Hunter