Clinical trial · Interventional
MR Guided Focused Ultrasound Surgery of Metastatic Bone Tumors
NCT00350233CI-TRIAL-00008037completedPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The objective of this trial is to evaluate the safety and effectiveness of MRgFUS in the treatment of metastatic bone tumors.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Bone Metastases | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| ExAblate 2000 | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- ExAblate MRgFUS
- interventionNames
- Device: ExAblate 2000
Primary outcomes (1)
- measure
- Determine safety of MRgFUS of Bone Metastases
- timeFrame
- Within 1 month of Treatment
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria: 1. Men and women age 18 and older 2. Patients who are able and willing to give consent and able to attend all study visits 3. Patients with histologically or cytologically confirmed malignant disease with a bone lesion that appears to be metastatic disease by clinical and or imaging techniques 4. Must have persistent pain from at least one site of bone metastases * Patient with VAS pain score ≥ 4, when VAS test taken without medication, OR * Patient taking pain-relieving medication for management of bone metastases. 5. Targeted tumor(s) are ExAblate device accessible 6. Targeted tumor(s) size is smaller than 8 cm in diameter 7. Patient whose lesion is on bone and is ≥ 10-mm from the skin. 8. Tumor(s) clearly visible by non-contrast MRI 9. Able to communicate sensations during the MRgFUS ExAblate treatment 10. At least 2 weeks since chemotherapy 11. At least 1 month since radiation therapy Exclusion Criteria: 1. Diffuse skeletal tumoral spread as evaluated by imaging. 2. Patients who need pre-treatment surgical stabilization of the affected bony structure. 3. Targeted tumor is in weight bearing bones or impending fracture 4. Targeted tumor is in the vertebral column. 5. Patients with unstable cardiac status including: * Unstable angina pectoris on medication * Patients with documented myocardial infarction within six months of protocol entry * Congestive heart failure requiring medication (other than diuretic) * Patients on anti-arrhythmic drugs 6. Severe hypertension (diastolic BP \> 100 on medication) 7. Patients with standard contraindications for MR imaging such as non-MRI compatible implanted metallic devices including cardiac pacemakers, size limitations (weight \>250 pounds), etc. 8. Known intolerance or allergies to the MRI contrast agent (e.g. Gadolinium or Magnevist) 9. ASA Score\>2 (See "Definitions" below) 10. Extensive scarring in an area in the path of energy planned passage to the treatment area 11. Severe cerebrovascular disease (multiple CVA or CVA within 6 months) 12. Patients on anti-coagulation therapy or those with an underlying bleeding disorder. 13. Individuals who are not able or willing to tolerate the required prolonged stationary position during treatment (approximately 3 hrs.) 14. Patient whose lesion is \< 10-mm from the skin 15. Patients with \< 2-Weeks since chemotherapy 16. Patient with \< 1-Month since radiation therapy 17. Patients with life expectancy \< 6-Months 18. Patients with surgical stabilization of tumor site with metallic hardware
References
Publications (0)
Data not yet available
No reference posted for this study.