Not provided
Not provided
Not provided
Not provided
the data collected are enough to obtain a qualitative analysis.
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Balloon Kyphoplasty is an alternative to vertebroplasty in the treatment of painful malignant vertebral fractures. This is a mini-invasive percutaneous treatment, aiming to stabilize the vertebral fracture, decrease of pain. This technique also improves patient function. Namely, bedridden patients are often able to resume walking in the days following vertebral cement injection. Advantage of Balloon Kyphoplasty as compared to vertebroplasty is the ability to inject the cement into the diseased vertebral body which shows cortical destruction with lower pressure, thereby possibly reducing cement leakage and related complications.
This is a multicentric, observational prospective study. Patients are evaluated before and after the procedure.
Sixty women or men older than 18 years, with 1 to 3 painful vertebral fracture(s) of malignant origin (due to multiple myeloma or osteolytic vertebral metastasis) will be enrolled. Each patient will be followed during 1 year after the procedure with 7 visits at D-8, D-1, D1, D15, D90, D180, and D360 or until the death of the patient.
The main evaluation outcome is patient self-global satisfaction regarding the procedure on a semi-quantitative satisfaction scale, 15 days after the Balloon Kyphoplasty.
Vertebral compression fractures (VCF) represent an important source of morbidity in patients presenting osteolytic metastatic or myelomatous vertebral involvement. In addition, cancer treatments may induce osteoporosis with an additional risk of vertebral fractures.
The two balloons (one on each side) should ideally be centered at middle height between the superior and inferior endplates and in the anterior two-thirds of the vertebral body. Balloon placement into the vertebral body is checked using radiopaque markers at the two extremities of the balloon. Once inserted, the balloons are inflated using visual, volume and pressure control to create a cavity. Inflation is stopped when one of the following inflation endpoints is reached: pressure raised over 400 psi, balloon contacts one of the cortical bone of the vertebra or reaching maximal balloon inflation volume. The balloons are then deflated and removed. The mean balloon inflation volume is 2 to 3ml. The Bone Filler Device, filled before with 1.5 ml of PMMA, is then advanced through the working cannula towards the anterior part of the cavity and cement is slowly extruded by a stainless steel stylet, acting as a plunger. When the amount of cement from the first Bone Filler Device is delivered in the cavity, it is removed and another Bone Filler Device is advanced through the working cannula. This step is repeated till a complete fill of the cavity is obtained. The same procedure is repeated through the other working cannula at the contra-lateral pedicle. Filling of the cavity with highly viscous PMMA is performed under continuous fluoroscopic control.
The aim of this study is to quantify the analgesic and patient function improvement of Balloon Kyphoplasty together with complication types and rate in patients with malignant vertebral fractures due to metastatic disease or multiple myeloma.
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| 1 | Experimental | balloon Kyphoplasty |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| balloon kyphoplasty | Device | A bilateral approach is chosen to insert working cannulas into the posterior part of the vertebral body through a posterior transpedicular approach.Once inserted, the balloons are inflated using visual, volume and pressure control to create a cavity.The balloons are then deflated and removed. The Bone Filler Device is then advanced through the working cannula towards the anterior part of the cavity and cement is slowly extruded by a stainless steel stylet, acting as a plunger. When the amount of cement from the first Bone Filler Device is delivered in the cavity, it is removed and another Bone Filler Device is advanced through the working cannula. |
| Measure | Description | Time Frame |
|---|---|---|
| Percentage of patients having a residual pain of ≤ 35mm on a VAS scale or a 50 % decrease in daily morphine dose at day 15 after Balloon Kyphoplasty compared to day 0 (day of procedure). | day 15 |
| Measure | Description | Time Frame |
|---|---|---|
| 1° Clinical Outcomes:· Pain evaluation using a visual analogic scale | D-8-D-1, D2 to D5, d15, D90, D180; D360 | |
| quality of life evaluation (SF 12). | D-8 to D-1, D2 to D5, D15, D90, D180; D360 | |
Not provided
Inclusion Criteria:
Male or female, 18 years or older
1 to 3 vertebral compression fracture(s), between T5-L5, responding to the following criteria:
The pain related to the fractured vertebrae is the more prevalent
More than 3 months life expectancy.
Blood Platelets rate more than or equal to 50 000/mm3 within the week before balloon kyphoplasty procedure (after a correct blood transfusion).
Patient must have signed a consent form.
Patient affiliated to social security
Exclusion Criteria:
Patient younger than 18
Impossibility to perform Balloon Kyphoplasty:
More than three symptomatic vertebral compression fractures in the same vertebral segment.
Patient receiving additional local treatment within 15 days after balloon kyphoplasty procedure (surgery, radiofrequency, radiotherapy).
Patient with primary bone tumors (eg : osteosarcoma) or single solitary plasmocytoma (patients presenting those tumors on other parts of the body, other than VCF are eligible).
Patients presenting sclerotic or mixed vertebral lesions(sclerotic vertebral lesions at another vertebral level are not a contraindication).
Patients with less than 3 month life expectancy
Patient undergoing an experimental anti-cancerous treatment in Phase I evaluated at the same time
Patient having relevant co-morbidities which may interfere with the data management on pain and quality of life.
Patient presenting an inadequate vertebra with Balloon Kyphoplasty.
Patient undergoing an additional treatment other than balloon kyphoplasty for their vertebral fracture.
Patient presenting neurological signs or spinal cord compression or spinal canal narrowing requiring surgical decompression;
Patient with a medical or surgical condition not compatible with balloon kyphoplasty procedure (eg : a non-treated local infection)
Patient having an allergy to the bone cement and/or to the contrast media used during the balloon kyphoplasty procedure.
Pregnant or breast feeding women
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Affiliation | Role |
|---|---|---|
| Jean-Denis LAREDO, M.D.,PR. | Assistance Publique - Hôpitaux de Paris | Study Director |
| Antoine FEYDY, M.D., PhD | Assistance Publique - Hôpitaux de Paris | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hôpital Henri Mondor - Service de Radiologie | Créteil | Val de Marne | 94000 | France | ||
| Hôpital Lariboisière-service de radiologie ostéoarticulaire |
Not provided
| ID | Term |
|---|---|
| D016103 | Spinal Fractures |
| D009101 | Multiple Myeloma |
| ID | Term |
|---|---|
| D013124 | Spinal Injuries |
| D019567 | Back Injuries |
| D014947 | Wounds and Injuries |
| D050723 | Fractures, Bone |
Not provided
Not provided
| ID | Term |
|---|---|
| D058498 | Kyphoplasty |
| ID | Term |
|---|---|
| D054854 | Vertebroplasty |
| D060826 | Cementoplasty |
| D019637 | Orthopedic Procedures |
| D013812 | Therapeutics |
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
|
| Assessment of the pain due to the compression fracture using a VAS scale in the same position as at the inclusion visit (standing or lying down), |
| D-8 to D-1, D2 to D5, D15, D90, D180; D360 |
| Assessment of the patient global satisfaction score using a LICKERT Scale, | D-8 to D-1, D2 to D5, D15, D90, D180; D360 |
| Percentage of patients who estimate than the pain due to the compression has decreased by more than 50% after the procedure, | day 15 |
| · Percentage of patients who give a positive answer to the following question: "would you agree to undergo a new Balloon Kyphoplasty in case you need it?" | D2 to D5, D15; D90 ; D180; D360 |
| Time elapsed between Balloon Kyphoplasty procedure and patient get up. | D2 to D5; D15;D90 |
| Resumption of the upright position for patients confined to bed due to their vertebral fracture | D2 to D5; D15 |
| Local and general complications related to cement leakage at each vertebral level treated. | each visit |
| 2° Radiological Outcomes: · Modification of the regional kyphosis angle measured by the Traumatic Regional Angle (ART - STAGNARA and NIEDERMANN) for compression fractures of T10 to L5 | D2to dJ5-d15-d90.-d180- d360 |
| Modification of the global Thoracic and lumbar kyphosis angles. | D2 to d5 - D15 - D90 - d180 - d360 |
| 3° Therapeutic Outcomes :· Need for radiation at day 30 after Balloon Kyphoplasty in patient presenting with Multiple Myeloma. | D30 |
| Paris |
| 75010 |
| France |
| Hôpital Cochin - service de radiologie | Paris | 75014 | France |
| Hopital Bichat -service de radiologie | Paris | 75018 | France |
| D054219 |
| Neoplasms, Plasma Cell |
| D009370 | Neoplasms by Histologic Type |
| D009369 | Neoplasms |
| D020141 | Hemostatic Disorders |
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
| D010265 | Paraproteinemias |
| D001796 | Blood Protein Disorders |
| D006402 | Hematologic Diseases |
| D006425 | Hemic and Lymphatic Diseases |
| D006474 | Hemorrhagic Disorders |
| D008232 | Lymphoproliferative Disorders |
| D007160 | Immunoproliferative Disorders |
| D007154 | Immune System Diseases |
| D013514 |
| Surgical Procedures, Operative |