Actively Recruiting
IlluminOss Photodynamic Bone Stabilization System for the Treatment of Impending and Actual Pelvis Fractures
Led by Massachusetts General Hospital · Updated on 2026-01-16
100
Participants Needed
1
Research Sites
314 weeks
Total Duration
On this page
Sponsors
M
Massachusetts General Hospital
Lead Sponsor
I
IlluminOss Medical, Inc.
Collaborating Sponsor
AI-Summary
What this Trial Is About
The aim of this project is to assess the effectiveness of the IlluminOss pelvic implants in patients with pelvic metastatic disease presenting with pain, risk of pathologic fracture, non-displaced or minimally displaced pathologic fracture of the pelvis, and geriatric patients with pelvic fragility fractures. Results from this study will be used to confirm preliminary clinically and possibly statistically significant reductions in pain and improvements in function among these patients.
CONDITIONS
Official Title
IlluminOss Photodynamic Bone Stabilization System for the Treatment of Impending and Actual Pelvis Fractures
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Skeletally mature patients aged 21 years or older receiving the FDA-approved IlluminOss Pelvic Implant
- Treatment intended for pain from impending or actual non-displaced or minimally displaced pelvic fractures due to metastatic malignancy, multiple myeloma, lymphoma, radiation osteitis, or pelvic fragility fractures in geriatric patients aged 65 or older
- Pain score of 30 or higher on a 0 to 100 scale
You will not qualify if you...
- Patients who are uncooperative or unable to follow directions due to neurological or psychiatric conditions
- Patients who are prisoners
- Patients deemed surgically unfit by the medical oncology service
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Massachusetts General Hospital
Boston, Massachusetts, United States, 02114
Actively Recruiting
Research Team
K
Kevin Raskin, MD
CONTACT
S
Shreya Halur, BS
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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