Trident Multi-tined Cannula for Cervical MBRFA Compared to the Conventional Cannula

NARecruitingINTERVENTIONAL
Enrollment

80

Participants

Timeline

Start Date

April 26, 2023

Primary Completion Date

June 30, 2026

Study Completion Date

October 31, 2026

Conditions
Cervical PainCervical Facet Joint Pain
Interventions
PROCEDURE

Cervical Medial Branch Radiofrequency Ablation

The skin and superficial tissues will be anesthetized at each site with 1-2 mL of lidocaine. Prior to the ablation up to 2 mL of lidocaine may be used at each site to ensure adequate pain control during the ablation. Once in position, a radiofrequency ablation lesion will be made using a 30 second ramp-up time to a maximum temperature of 80 °C, followed by an additional 90 seconds at maximum temperature.

Trial Locations (3)

84009

RECRUITING

University of Utah South Jordan Health Center, South Jordan

84025

RECRUITING

University of Utah Farmington Health Center, Farmington

84108

RECRUITING

University of Utah Orthopaedic Center, Salt Lake City

All Listed Sponsors
lead

University of Utah

OTHER

NCT05424198 - Trident Multi-tined Cannula for Cervical MBRFA Compared to the Conventional Cannula | Biotech Hunter | Biotech Hunter