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Treatment of Malignant Vertebral Fractures With Percutaneous Balloon Kyphoplasty. (KYPHOK)

Primary Purpose

Vertebral Fracture, Multiple Myeloma, Osteolytic Metastases

Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
balloon kyphoplasty
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vertebral Fracture focused on measuring Vertebral fracture, Vertebral compression fracture, Multiple Myeloma Bone marrow diseases, Vertebral metastases, Balloon Kyphoplasty

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Male or female, 18 years or older
  2. 1 to 3 vertebral compression fracture(s), between T5-L5, responding to the following criteria:

    • at least 15% loss of vertebral body height (anterior, median or posterior);
    • malignant origin (bone metastases, multiple myeloma, hemopathy) assessed by imaging, including an MRI and a CT-SCAN of less than 4 weeks.
    • Pain or painful deterioration less than 3 months old, related to one or more vertebral fractures with a VAS higher than 50/100 mm when changing position, or higher than 40/100 mm if associated with morphine ≥ 30 mg/day ;
  3. The pain related to the fractured vertebrae is the more prevalent
  4. More than 3 months life expectancy.
  5. Blood Platelets rate more than or equal to 50 000/mm3 within the week before balloon kyphoplasty procedure (after a correct blood transfusion).
  6. Patient must have signed a consent form.
  7. Patient affiliated to social security

Exclusion Criteria:

  1. Patient younger than 18
  2. Impossibility to perform Balloon Kyphoplasty:

    • Technical impossibility to achieve the percutaneous approach to the vertebra to treat.
    • Vertebral pedicle diameter or height of treated vertebra(e) not sufficient regarding balloon kyphoplasty TROCATHETER size. This should be assessed through prescreening MRI and/or CT-Scan
  3. More than three symptomatic vertebral compression fractures in the same vertebral segment.
  4. Patient receiving additional local treatment within 15 days after balloon kyphoplasty procedure (surgery, radiofrequency, radiotherapy).
  5. 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).
  6. Patients presenting sclerotic or mixed vertebral lesions(sclerotic vertebral lesions at another vertebral level are not a contraindication).
  7. Patients with less than 3 month life expectancy
  8. Patient undergoing an experimental anti-cancerous treatment in Phase I evaluated at the same time
  9. Patient having relevant co-morbidities which may interfere with the data management on pain and quality of life.
  10. Patient presenting an inadequate vertebra with Balloon Kyphoplasty.
  11. Patient undergoing an additional treatment other than balloon kyphoplasty for their vertebral fracture.
  12. Patient presenting neurological signs or spinal cord compression or spinal canal narrowing requiring surgical decompression;
  13. Patient with a medical or surgical condition not compatible with balloon kyphoplasty procedure (eg : a non-treated local infection)
  14. Patient having an allergy to the bone cement and/or to the contrast media used during the balloon kyphoplasty procedure.
  15. Pregnant or breast feeding women

Sites / Locations

  • Hôpital Henri Mondor - Service de Radiologie
  • Hôpital Lariboisière-service de radiologie ostéoarticulaire
  • Hôpital Cochin - service de radiologie
  • Hopital Bichat -service de radiologie

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

1

Arm Description

balloon Kyphoplasty

Outcomes

Primary Outcome Measures

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).

Secondary Outcome Measures

1° Clinical Outcomes:· Pain evaluation using a visual analogic scale
quality of life evaluation (SF 12).
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),
Assessment of the patient global satisfaction score using a LICKERT Scale,
Percentage of patients who estimate than the pain due to the compression has decreased by more than 50% after the procedure,
· 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?"
Time elapsed between Balloon Kyphoplasty procedure and patient get up.
Resumption of the upright position for patients confined to bed due to their vertebral fracture
Local and general complications related to cement leakage at each vertebral level treated.
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
Modification of the global Thoracic and lumbar kyphosis angles.
3° Therapeutic Outcomes :· Need for radiation at day 30 after Balloon Kyphoplasty in patient presenting with Multiple Myeloma.

Full Information

First Posted
September 5, 2008
Last Updated
March 23, 2015
Sponsor
Assistance Publique - Hôpitaux de Paris
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1. Study Identification

Unique Protocol Identification Number
NCT00748631
Brief Title
Treatment of Malignant Vertebral Fractures With Percutaneous Balloon Kyphoplasty.
Acronym
KYPHOK
Official Title
Assessment of Percutaneous Balloon Kyphoplasty in the Treatment of Malignant Vertebral Fractures (Multiple Myeloma and Osteolytic Metastases) : "Observational Study"
Study Type
Interventional

2. Study Status

Record Verification Date
November 2014
Overall Recruitment Status
Terminated
Why Stopped
the data collected are enough to obtain a qualitative analysis.
Study Start Date
October 2007 (undefined)
Primary Completion Date
November 2009 (Actual)
Study Completion Date
November 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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. Current medical treatments are symptomatic. They do not treat the fracture itself. Vertebroplasty is an interventional radiological technique that consists of injecting, percutaneously, acrylic cement into the fractured vertebra under radiological guidance and local or general anaesthesia, in order to combine two effects: stabilization of the vertebral body fracture and pain reduction. Balloon Kyphoplasty is a variant of vertebroplasty which is performed using the KyphX® System (Medtronic., Sunnyvale, California). Balloon kyphoplasty aims at restore vertebral height of the fractured vertebra using an inflatable balloon prior to inject surgical polymethylmetacrylate (PMMA)cement,into the vertebral body to fix the fracture. It is an expensive technique costing around 4,000 euros for up to 2 vertebrae in the same patient. The surgical technique for the procedure has been described by LIBERMEAN et al: A bilateral approach is usually chosen to insert working cannulas into the posterior part of the vertebral body through a posterior transpedicular approach. In case of limited and asymmetric vertebral destruction, a single unilateral approach may be preferred. Fluoroscopy is used to insert the tools and control the procedure. With reaming tools, two working channels are created and the balloons are inserted. The balloons are available in lengths of 10, 15 and 20 mm. 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vertebral Fracture, Multiple Myeloma, Osteolytic Metastases
Keywords
Vertebral fracture, Vertebral compression fracture, Multiple Myeloma Bone marrow diseases, Vertebral metastases, Balloon Kyphoplasty

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
balloon Kyphoplasty
Intervention Type
Device
Intervention Name(s)
balloon kyphoplasty
Intervention Description
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.
Primary Outcome Measure Information:
Title
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).
Time Frame
day 15
Secondary Outcome Measure Information:
Title
1° Clinical Outcomes:· Pain evaluation using a visual analogic scale
Time Frame
D-8-D-1, D2 to D5, d15, D90, D180; D360
Title
quality of life evaluation (SF 12).
Time Frame
D-8 to D-1, D2 to D5, D15, D90, D180; D360
Title
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),
Time Frame
D-8 to D-1, D2 to D5, D15, D90, D180; D360
Title
Assessment of the patient global satisfaction score using a LICKERT Scale,
Time Frame
D-8 to D-1, D2 to D5, D15, D90, D180; D360
Title
Percentage of patients who estimate than the pain due to the compression has decreased by more than 50% after the procedure,
Time Frame
day 15
Title
· 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?"
Time Frame
D2 to D5, D15; D90 ; D180; D360
Title
Time elapsed between Balloon Kyphoplasty procedure and patient get up.
Time Frame
D2 to D5; D15;D90
Title
Resumption of the upright position for patients confined to bed due to their vertebral fracture
Time Frame
D2 to D5; D15
Title
Local and general complications related to cement leakage at each vertebral level treated.
Time Frame
each visit
Title
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
Time Frame
D2to dJ5-d15-d90.-d180- d360
Title
Modification of the global Thoracic and lumbar kyphosis angles.
Time Frame
D2 to d5 - D15 - D90 - d180 - d360
Title
3° Therapeutic Outcomes :· Need for radiation at day 30 after Balloon Kyphoplasty in patient presenting with Multiple Myeloma.
Time Frame
D30

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female, 18 years or older 1 to 3 vertebral compression fracture(s), between T5-L5, responding to the following criteria: at least 15% loss of vertebral body height (anterior, median or posterior); malignant origin (bone metastases, multiple myeloma, hemopathy) assessed by imaging, including an MRI and a CT-SCAN of less than 4 weeks. Pain or painful deterioration less than 3 months old, related to one or more vertebral fractures with a VAS higher than 50/100 mm when changing position, or higher than 40/100 mm if associated with morphine ≥ 30 mg/day ; 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: Technical impossibility to achieve the percutaneous approach to the vertebra to treat. Vertebral pedicle diameter or height of treated vertebra(e) not sufficient regarding balloon kyphoplasty TROCATHETER size. This should be assessed through prescreening MRI and/or CT-Scan 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-Denis LAREDO, M.D.,PR.
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Antoine FEYDY, M.D., PhD
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital Henri Mondor - Service de Radiologie
City
Creteil
State/Province
Val de Marne
ZIP/Postal Code
94000
Country
France
Facility Name
Hôpital Lariboisière-service de radiologie ostéoarticulaire
City
Paris
ZIP/Postal Code
75010
Country
France
Facility Name
Hôpital Cochin - service de radiologie
City
Paris
ZIP/Postal Code
75014
Country
France
Facility Name
Hopital Bichat -service de radiologie
City
Paris
ZIP/Postal Code
75018
Country
France

12. IPD Sharing Statement

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Treatment of Malignant Vertebral Fractures With Percutaneous Balloon Kyphoplasty.

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