MRgFUS in the Treatment of Hand and Hip Osteoarthritic Pain
Primary Purpose
Osteoarthritis, Hip Osteoarthritis, Hand Osteoarthritis
Status
Completed
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
MRgFUS treatment
MRgFUS treatment
Sponsored by
About this trial
This is an interventional treatment trial for Osteoarthritis focused on measuring MRgFUS, Pain, Hip, Trapeziometacarpal joint, Osteoarthritis
Eligibility Criteria
Inclusion Criteria:
- Male and female aged between 45 and 90 years
- Presence of activity-related joint pain
- Patients who have either no morning joint-related stiffness or morning stiffness that lasts no longer than 30 minutes
- Patients who have not responded to previous treatments,
- Patients with a baseline pain intensity of 4 to 8 on a 10-cm VAS
- Patients who are not candidates for immediate surgery
- Signed statement of informed consent (approved by Ethics Committee)
Exclusion Criteria:
- Prior surgery or previous local treatment (infiltration, other) in the past 3 months
- Changes in medications used during the previous 2 months
- Intravenous drug use
- Corticosteroid use of more than 3 months within the preceding year
- Diagnosis of other rheumatologic disorders
- Trauma, fracture, or osteomyelitis of the investigated joints within the preceding year
- Any neurological disease or disorders potentially affecting pain perception
- Fibromyalgia
- Pregnancy
- Patients with large scar at skin or deeper soft tissue potentially included in the planned path of the ultrasound beam
- General contraindications to MRI and/or to anaesthesiological procedures planned for the patient
- Presence of internal hardware or devices potentially affecting MR thermometry
Sites / Locations
- Istituto Ortopedico Rizzoli
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Hand ExAblate
Hip ExAblate
Arm Description
MRgFUS treatment of pain caused by trapeziometacarpal OA (and/or scaphotrapezial OA)
MRgFUS treatment of pain caused by hip OA
Outcomes
Primary Outcome Measures
Changes in Pain Intensity from Baseline
Changes in pain intensity from baseline will be determined by a straight horizontal 10-cm linear Visual Analog Pain Scale (VAS, scale 0-10 where 0 means 'no pain at all' and 10 means 'pain as bad as it could be').
Incidence of Treatment-Related Adverse Events (Safety and Tolerability)
Collecting the number of treatment-related adverse events
Secondary Outcome Measures
Full Information
NCT ID
NCT03467165
First Posted
February 23, 2018
Last Updated
May 10, 2023
Sponsor
Istituto Ortopedico Rizzoli
1. Study Identification
Unique Protocol Identification Number
NCT03467165
Brief Title
MRgFUS in the Treatment of Hand and Hip Osteoarthritic Pain
Official Title
Magnetic Resonance Guided Focused Ultrasound Surgery: a Pilot Study in the Treatment of Pain Caused by Osteoarthritis - Hand and Hip, Challenging Joints
Study Type
Interventional
2. Study Status
Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
April 27, 2019 (Actual)
Primary Completion Date
March 15, 2020 (Actual)
Study Completion Date
March 15, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Istituto Ortopedico Rizzoli
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This project aims at performing a pilot study to provide data on safety and potential efficacy of Magnetic Resonance guided Focused Ultrasound Surgery (MRgFUS) in the treatment of pain caused by trapeziometacarpal osteoarthritis (OA) and/or scaphotrapezial OA, and by hip OA, while exploring the potential application of MRgFUS to two different and central joints burdened by OA.
Detailed Description
Pain caused by osteoarthritis is a matter of huge impact, in terms of quality of life, social and economic burden. Global aging of the population is going to worsen the problem. The hand is the most affected site in the upper limb, and involvement of the trapeziometacarpal joint is highly prevalent, with significant limitation of functionality when it happens. In the lower limb, the hip and the knee share the leading position in the clinical scenario, with the former being historically the most frequently submitted to joint replacement.
At any site, the vast majority of joint replacement surgery procedures are performed because of pain. MRgFUS has recently demonstrated a great potential in treating pain caused by different medical conditions, including osteoarthritis. The aim of the work is to study the feasibility, the safety and the potential efficacy of MRgFUS in treating pain from osteoarthritis in two "hot" spots: the hip and the trapeziometacarpal/scaphotrapezial joint.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis, Hip Osteoarthritis, Hand Osteoarthritis
Keywords
MRgFUS, Pain, Hip, Trapeziometacarpal joint, Osteoarthritis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Pilot study
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
14 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Hand ExAblate
Arm Type
Experimental
Arm Description
MRgFUS treatment of pain caused by trapeziometacarpal OA (and/or scaphotrapezial OA)
Arm Title
Hip ExAblate
Arm Type
Experimental
Arm Description
MRgFUS treatment of pain caused by hip OA
Intervention Type
Device
Intervention Name(s)
MRgFUS treatment
Intervention Description
MRgFUS treatment of pain caused by trapeziometacarpal OA (and/or scaphotrapezial OA)
Intervention Type
Device
Intervention Name(s)
MRgFUS treatment
Intervention Description
MRgFUS treatment of pain caused by hip OA
Primary Outcome Measure Information:
Title
Changes in Pain Intensity from Baseline
Description
Changes in pain intensity from baseline will be determined by a straight horizontal 10-cm linear Visual Analog Pain Scale (VAS, scale 0-10 where 0 means 'no pain at all' and 10 means 'pain as bad as it could be').
Time Frame
Baseline (Day1), Week 1, 2, 3, Month 1, 2, 3, 6, 9, 12
Title
Incidence of Treatment-Related Adverse Events (Safety and Tolerability)
Description
Collecting the number of treatment-related adverse events
Time Frame
Through study completion, an average of 1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Male and female aged between 45 and 90 years
Presence of activity-related joint pain
Patients who have either no morning joint-related stiffness or morning stiffness that lasts no longer than 30 minutes
Patients who have not responded to previous treatments,
Patients with a baseline pain intensity of 4 to 8 on a 10-cm VAS
Patients who are not candidates for immediate surgery
Signed statement of informed consent (approved by Ethics Committee)
Exclusion Criteria:
Prior surgery or previous local treatment (infiltration, other) in the past 3 months
Changes in medications used during the previous 2 months
Intravenous drug use
Corticosteroid use of more than 3 months within the preceding year
Diagnosis of other rheumatologic disorders
Trauma, fracture, or osteomyelitis of the investigated joints within the preceding year
Any neurological disease or disorders potentially affecting pain perception
Fibromyalgia
Pregnancy
Patients with large scar at skin or deeper soft tissue potentially included in the planned path of the ultrasound beam
General contraindications to MRI and/or to anaesthesiological procedures planned for the patient
Presence of internal hardware or devices potentially affecting MR thermometry
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alberto Bazzocchi, MD, PhD
Organizational Affiliation
The Rizzoli Ortopaedic Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Istituto Ortopedico Rizzoli
City
Bologna
State/Province
BO
ZIP/Postal Code
40136
Country
Italy
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
MRgFUS in the Treatment of Hand and Hip Osteoarthritic Pain
We'll reach out to this number within 24 hrs