Purpose

Compile real-world outcomes of commercially approved Intracept™ Intraosseous Nerve Ablation Systems in the treatment of patients diagnosed with vertebrogenic pain.

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Study candidate is scheduled to be treated with a commercially approved Intracept™ Intraosseous Nerve Ablation System per local Instructions for Use (IFU). - Signed a valid, IRB/EC-approved informed consent form.

Exclusion Criteria

  • Meets any contraindications per locally applicable Instructions for Use (IFU).

Study Design

Phase
Study Type
Observational [Patient Registry]
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Intracept™ Intraosseous Nerve Ablation Systems Subjects with pain treated with a commercially approved Intracept™ Intraosseous Nerve Ablation System
  • Device: Intracept™ Intraosseous Nerve Ablation
    Intracept™ Intraosseous Nerve Ablation for treatment of patients diagnosed with vertebrogenic pain

Recruiting Locations

Flagstaff Bone & Joint
Flagstaff, Arizona 86001
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

Innovative Pain and Wellness
Phoenix, Arizona 85014
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

MarinHealth Spine Institute
Larkspur, California 94939
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

Stanford University Medical Center
Stanford, California 94305
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

The Spine Wellness Center in Westport
Westport, Connecticut 06880
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

Washington Hospital Center
Washington D.C., District of Columbia 20010
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

Orlando Regional Medical Center
Orlando, Florida 32806
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

Horizon Clinical Research, LLC
Jasper, Georgia 30143
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

Illinois Bone and Joint Institute
Barrington, Illinois 60010
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

Commonwealth Pain and Spine
Lexington, Kentucky 40509
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

Ochsner Clinic Foundation
New Orleans, Louisiana 70115
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

iSpine Clinics
Maple Grove, Minnesota 55369
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

CentraCare Health System
Saint Cloud, Minnesota 56303
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

New York Spine and Pain Specialists
Port Jefferson Station, New York 11776
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

University of Rochester
Rochester, New York 14618
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

Novant Health Spine Specialists
Bermuda Run, North Carolina 27106
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

Allegheny General Hospital
Pittsburgh, Pennsylvania 15212
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

Cy-Pain and Spine
Houston, Texas 77065
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

University of Utah Orthopaedic Center
Salt Lake City, Utah 84108
Contact:
Boston Scientific Clinical Research
855-213-9890
BSNClinicalTrials@bsci.com

More Details

Status
Recruiting
Sponsor
Boston Scientific Corporation

Study Contact

Ann Yamano
855-213-9890
BSNClinicalTrials@bsci.com

Detailed Description

The objective of this study is to compile real-world outcomes of commercially approved Intracept™ Intraosseous Nerve Ablation Systems in the treatment of patients diagnosed with vertebrogenic pain.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.