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DECISION OF THE SPONSOR AND THE COORDINATING INVESTIGATOR DUE TO RECRUITMENT DIFFICULTIES AND CHANGES IN INTERVENTIONAL RADIOLOGY PRACTICES
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Conventional vertebroplasty is an effective option in the treatment of bone lesions (osteoporotic and neoplastic). It is indicated as an analgesic treatment and aims at reinforcing a compressed vertebrae or at risk of fracture.
The main adverse event related to vertebroplasty use is the cement leakages that might be responsible for significant clinical impairments.
Kyphoplasty is a recent alternative strategy of vertebroplasty, based on the insertion on balloon through the needle into the targeted vertebrae and then inflation of the balloon prior to cement injection into the space.
In an osteoporotic setting, kyphoplasty allow reducing the incidence of cement leakage.
To date, no data from randomized study are available in the population of cancer patients.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Conventional vertebroplasty | Active Comparator | Conventional vertebroplasty (device's trade at the discretion of the investigator) |
|
| Kyphoplasty | Experimental | Vertebroplasty with balloon placement and inflation prior to cement injection (device's trade at the discretion of the investigator) |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Kyphoplasty | Device | Placement and inflation of balloon prior to cement injection |
|
| Measure | Description | Time Frame |
|---|---|---|
| Success rate for each strategy | The success rate will be calculated with the proportion of patients without cement leakage | 3 months after the procedure |
| Measure | Description | Time Frame |
|---|---|---|
| Height of the targeted vertebrae | 3 months after the procedure | |
| Height of the patient | 3 months after the procedure | |
| Kyphotic angle |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Amine BOUHAMAMA, MD | Centre Leon Berard | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Centre Léon Bérard | Lyon | 69008 | France | |||
| Hopital Nord |
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| ID | Term |
|---|---|
| D058498 | Kyphoplasty |
| D054854 | Vertebroplasty |
| ID | Term |
|---|---|
| D060826 | Cementoplasty |
| D019637 | Orthopedic Procedures |
| D013812 | Therapeutics |
| D013514 | Surgical Procedures, Operative |
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| Conventional vertebroplasty | Device | Conventional vertebroplasty |
|
|
| 3 months after the procedure |
| Analgesic properties of the strategies the day after the procedure | Pain will be assessed using a Visual Analogic Scale | The day after the procedure |
| Analgesic properties of the strategies at 21 days | Pain will be assessed using a Visual Analogic Scale | 21 days after the procedure |
| Analgesic properties of the strategies at the end of the study | Pain will be assessed using a Visual Analogic Scale | 3 months after the procedure |
| Tolerance profile of the strategies | Tolerance will be evaluated according to the National Cancer Institute - Common Terminology Criteria Adverse Event grading scale version 4 | Through study completion |
| Type of cement leakage (vascular versus cortical localisation) | Location will be described as vascular or cortical using the imaging assessments | 3 months after the procedure |
| Size of cement leakage | Size will be described as significant or not significant as per investigator judgement | 3 months after the procedure |
| Symptoms associated with cement leakage | Symptoms associated with cement leakage will be tolerance events that are stated by the investigator as related to a cement leakage | 3 months after the procedure |
| Quality of Life in both arms at Day 21 | Quality of Life will be assessed with the Dallas questionnaire for spinal pain | 21 days after procedure |
| Quality of Life in both arms at the end oh study | Quality of Life will be assessed with the Dallas questionnaire for spinal pain | 3 months after the procedure |
| Correlation between volume of cement injected and the level of pain relief using the Visual Analogic Scale | 3 months after the procedure |
| Saint-Etienne |
| 42270 |
| France |