NCT07561489
A Prospective, Single-center, Observational Clinical Outcomes Study for Vertebral Compression Fractures Treated With the OsteoPearl Biological Allograft Implants
Enrolling by Invitation
Not specifiedAges 50+ObservationalLenoss Medical
~25 participants
Updated 2026-05-01 on ClinicalTrials.gov
What's tested:Allograft
At a glance
Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Fracture Stability Evaluation
Measured over 30 days
Conditions
Where it's being run
1 sites across 1 statesNew York1
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
What this trial measures
- Fracture Stability Evaluation30 days
The primary objective of this study is to evaluate fracture stability through longitudinal assessment of subject-reported pain following treatment with the OsteoPearl Biological Allograft. Pain intensity will be measured using the Numerical Rating Scale (NRS) for back pain.