Abaloparatide for Bone Quality in Lumbar Degenerative Disease
This study is looking at how a medication called abaloparatide affects bone quality in people with osteoporosis (a condition where bones become weak and brittle) who are having spinal fusion and decompression surgery for lumbar degenerative disease (problems with the lower back). Researchers want to see if abaloparatide improves bone density, as measured by a special score called VBQ, and if it helps reduce problems after surgery, like complications with the spinal hardware. You might be able to join if you are 50 or older, have osteoporosis based on certain criteria (like a fragility fracture or a low T-score), and are scheduled for this type of back surgery. The study aims to enroll 60 participants. The current status of the study is unclear.
- Study design
- This is an interventional study, meaning participants will receive a specific treatment. It plans to enroll 60 participants.
- What's involved
- Participants will receive 3-6 months of abaloparatide treatment and will be trained on how to apply it. They will also have presurgical assessments.
- Compensation
- Not stated in the trial record.
- Follow-up
- Bone quality will be measured at 6 weeks post-operation.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
The Effect of Osteoporotic Medications on Vertebral Bone Quality Score
At a glance
Conditions
Where it's being run
1 sites across 1 statesWho to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.
Inclusion
Exclusion
What this trial measures
- Improvement in Bone Quality6 weeks post-op
Improvement in bone quality, using Vertebral Bone Quality
- Improvement in Bone Quality6 weeks post-op
Improvement in bone quality, using Hounsfield Units
- Improvement in Bone Quality6 weeks post-op
Improvement in bone quality, using DEXA (Dual-Energy X-ray ABsorptiometry)
- Improvement in Bone Quality6 months post-op
Improvement in bone quality, using Vertebral Bone Quality
- Improvement in Bone Quality6 months post-op
Improvement in bone quality, using Hounsfield Units
- Improvement in Bone Quality6 months post-op
Improvement in bone quality, using DEXA (Dual-Energy X-ray ABsorptiometry)
- Improvement in Bone Quality12 months post-op
Improvement in bone quality, using Vertebral Bone Quality
- Improvement in Bone Quality12 months post-op
Improvement in bone quality, using Hounsfield Units
- Improvement in Bone Quality12 months post-op
Improvement in bone quality, using DEXA (Dual-Energy X-ray ABsorptiometry)
- Improvement in Bone Quality24 months post-op
Improvement in bone quality, using Vertebral Bone Quality
- Improvement in Bone Quality24 months post-op
Improvement in bone quality, using Hounsfield Units
- Improvement in Bone Quality24 months post-op
Improvement in bone quality, using DEXA (Dual-Energy X-ray ABsorptiometry)