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VERTOS-II. Percutaneous Vertebroplasty Versus Conservative Therapy

This study is ongoing, but not recruiting participants.

Sponsors and Collaborators: UMC Utrecht
ZonMw: The Netherlands Organisation for Health Research and Development
Information provided by: UMC Utrecht
ClinicalTrials.gov Identifier: NCT00232466
  Purpose

Percutaneous vertebroplasty is a new procedure for treating painful osteoporotic compression fractures of the spine. Five-thousand out of 12.000 patients (16.000 vertebral fractures/year in the Netherlands) present with sudden, severe back pain in the region of the fracture.Until recently, bed rest, analgesia and physical support were the only treatment options. After decades of performing PV, no large RCT with mid-term follow-up has been published.

Design:

This will be a multicenter (6 centers), prospective, randomised, intervention study. Eligible patients will be randomised for percutaneous vertebroplasty or conservative therapy.

Study population:

Age: 50 and older, vertebral fracture, level: thoracic vertebral body 5 (Th 5) or lower, osteopenia (T-score < -1 SD), back pain for no more than 6 weeks and edema in the vertebrae on MR imaging

Statistical analyses All analyses will be performed on an 'intention to treat' principle. The planned number of subjects will be 200 in total, 100 in each intervention arm.

Economic evaluation:

Cost-effectiveness will be assessed. The costs of the procedure and the medical treatment, and of visits to medical specialists, GP's and physical therapists will be compared.

Time schedule:

The total study will take 36 months

Recruitment of patients (200) has been completed. In May 2009 the 1 year follow-up will be finished.


Condition Intervention
Osteoporosis
Back Pain
Procedure: Vertebroplasty

MedlinePlus related topics:   Back Pain    Fractures    Osteoporosis   

ChemIDplus related topics:   Risedronate sodium    Risedronic acid   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Safety/Efficacy Study
Official Title:   VERTOS II. Percutaneous Vertebroplasty Versus Conservative Therapy in Patients With Osteoporotic Vertebral Fractures

Further study details as provided by UMC Utrecht:

Primary Outcome Measures:
  • To compare the cost-effectivity in the two groups [ Time Frame: 1 month, 1 year ] [ Designated as safety issue: No ]
  • VAS score in time [ Time Frame: 1 month, 1 year ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • To compare pain relief and the quality of life of the patients in the two groups. [ Time Frame: 1 day, 1 week, 1 month, 3 months, 6 months, 12 months and 24 months ] [ Designated as safety issue: No ]

Enrollment:   200
Study Start Date:   October 2005
Estimated Study Completion Date:   May 2010
Estimated Primary Completion Date:   May 2009 (Final data collection date for primary outcome measure)

Arms Assigned Interventions
2: No Intervention
conservative therapy (no intervention)
1: Active Comparator
Vertebroplasty
Procedure: Vertebroplasty

Procedure:

The treatment consists of a transpedicular injection of polymethylmethacrylate bone cement into the collapsed vertebral body (maximal 2 vertebrae in 1 treatment session) using fluoroscopic guidance. The procedure is performed under the use of local anesthetics and the patient can be discharged the same day or after 1 night of hospital stay.


Show detailed description  Show Detailed Description

  Eligibility
Ages Eligible for Study:   50 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion criteria:

  • age: 50 and older
  • vertebral fracture: 15-85% height loss
  • level: thoracic vertebral body 5 (Th 5) or lower
  • osteopenia (T-score < -1 SD)
  • back pain for at least no longer than 6 weeks
  • edema in the vertebrae on MR imaging

Exclusion criteria:

  • complete loss of vertebral body height
  • fracture through or destruction of the posterior vertebral wall
  • pressure of bone fragments on the spinal cord
  • osteomyelitis or spondylodiscitis
  • vertebral column neoplasms
  • uncorrectable coagulation disorder
  • medical conditions that would make the patient ineligible for emergency decompressive surgery should it be necessary to treat a complication of the procedure
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00232466

Locations
Belgium
AZ St. Lucas Ziekenhuis    
      Gent, Belgium, 9000
Netherlands
St. Elisabeth Ziekenhuis    
      Tilburg, Netherlands, 5022 GC
Catharina-Ziekenhuis    
      Eindhoven, Netherlands, 5623 EJ
Albert Schweizer Ziekenhuis    
      Dordrecht, Netherlands, 3300 AK
UMCU    
      Utrecht, Netherlands, 3508 GA
Netherlands, Utrecht
Diakonessenhuis    
      Utrecht/Zeist/Doorn, Utrecht, Netherlands, 3508 TG

Sponsors and Collaborators
UMC Utrecht
ZonMw: The Netherlands Organisation for Health Research and Development

Investigators
Principal Investigator:     Willem Mali, MD.PhD     UMC Utrecht    
  More Information


information about vertebroplasty  This link exits the ClinicalTrials.gov site
 

Responsible Party:   UMC Utrecht ( Caroline Klazen )
Study ID Numbers:   945-06-351, 945-06-351
First Received:   September 30, 2005
Last Updated:   June 24, 2008
ClinicalTrials.gov Identifier:   NCT00232466
Health Authority:   Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)

Keywords provided by UMC Utrecht:
Vertebroplasty  
Vertebral fracture  
Actonel  
Osteoporotic
vertebral
fractures

Study placed in the following topic categories:
Polymethyl Methacrylate
Signs and Symptoms
Musculoskeletal Diseases
Fractures, Bone
Spinal Fractures
Neurologic Manifestations
Osteoporosis
Bone Diseases, Metabolic
Pain
Bone Diseases
Back Pain
Risedronic acid

Additional relevant MeSH terms:
Nervous System Diseases

ClinicalTrials.gov processed this record on October 03, 2008




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