Embo Registry; National Registry for Artery Embolization

Last updated: October 24, 2024
Sponsor: Vascular Solutions of North Carolina
Overall Status: Active - Recruiting

Phase

N/A

Condition

Chronic Pain

Osteoarthritis

Pain

Treatment

Artery Embolization

Clinical Study ID

NCT06477965
20241915
  • Ages > 18
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

Embo Registry is a retrospective and prospective observational study to evaluate real world effectiveness and the use of Artery Embolization as a treatment for chronic pain with patients that have osteoarthritis and localized pain to provide symptomatic relief. This study is to determine the efficacy and validity of procedure and that following procedure patients had decreased pain and improved quality of life.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • > 18 years of age undergone artery embolization interventions for the treatment ofchronic pain due to osteoarthritis or other diagnoses that cause localized pain.

Exclusion

Exclusion Criteria:

  • None

Study Design

Total Participants: 1000
Treatment Group(s): 1
Primary Treatment: Artery Embolization
Phase:
Study Start date:
July 15, 2024
Estimated Completion Date:
July 15, 2029

Study Description

Embolic Solution are intended for use in occluding blood vessels for therapeutic or operative purposes. The embolic solution is used during an outpatient procedure, the physician will insert a small catheter onto the artery supplying the lining of the target joint or target localized pain. Tiny particles are then injected through the catheter into these arteries, reducing blood flow to the target area. This reduces the amount of inflammation associated with osteoarthritis, tendonitis, tenosynovitis or an injury, a process that can help decrease symptoms or eliminate the associated localized pain to this area. With understanding that it does not treat the underlying cartilage destruction or underlying condition causing pain but would like to determine the efficacy and validity of this treatment. For the study to determine efficacy and overall improvement of patients post procedure by comparing patient's pain preoperative and post operatively, if there is a decreased use of medication preoperatively compared to post procedure and increased quality of life preoperative and post procedure. Clinical outcomes of improvement will be determined by improvement of Visual Analog Scale (VAS) scores, Western Ontario and McMaster Universities Index (WOMAC), EQ-5D-5L Quality of Life Questionnaire, and to determine if patients had decrease used of medication prescribed preoperatively.

Connect with a study center

  • Vascular Solutions of North Carolina

    Cary, North Carolina 27518
    United States

    Active - Recruiting

  • Southern Tennessee Cardiology

    Winchester, Tennessee 37398
    United States

    Active - Recruiting

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