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Effect and Essentiality of Vertebroplasty Surgery in Acute Vertebral Compression Fractures

Primary Purpose

Spinal Fractures

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
percutaneous vertebroplasty
conservative treatment
Sponsored by
Peking University People's Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Spinal Fractures focused on measuring Spinal Fractures/surgery, Vertebroplasty, Quality-Adjusted Life Years

Eligibility Criteria

50 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • vertebral compression fracture on spine radiograph (minimum 15% height loss)
  • level of fracture at Th5 or lower; back pain for 6 weeks or less
  • focal tenderness at fracture level on physical examination
  • bone oedema of vertebral fracture on MRI
  • decreased bone density (T scores ≤-1)

Exclusion Criteria:

  • severe cardiopulmonary comorbidity
  • suspected underlying malignant disease
  • radicular syndrome
  • spinal-cord compression syndrome
  • contraindication for radiography exam

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Active Comparator

    Arm Label

    grade 1

    grade 2

    Arm Description

    percutaneous vertebroplasty

    conservative treatment

    Outcomes

    Primary Outcome Measures

    change of pain relief
    World Health Organization pain classification

    Secondary Outcome Measures

    quality of life
    Quality of Life Questionnaire of the European Foundation for Osteoporosis (QUALEFFO)

    Full Information

    First Posted
    November 25, 2017
    Last Updated
    December 2, 2017
    Sponsor
    Peking University People's Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03360383
    Brief Title
    Effect and Essentiality of Vertebroplasty Surgery in Acute Vertebral Compression Fractures
    Official Title
    Effect and Essentiality of Vertebroplasty Surgery in Acute Vertebral Compression Fractures: a Multiple Center Randomized Controlled Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    December 2017
    Overall Recruitment Status
    Unknown status
    Study Start Date
    February 1, 2018 (Anticipated)
    Primary Completion Date
    January 1, 2020 (Anticipated)
    Study Completion Date
    June 1, 2020 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Peking University People's Hospital

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Percutaneous vertebroplasty is now a common procedures of patients with acute osteoporotic vertebral compression fractures in medical units all over China, but the efficacy and essentiality of the surgery remain uncertain and is the subject of this study. This is a multiple center open-label randomised trial. Patients were randomly allocated to percutaneous vertebroplasty or conservative treatment. Because of the procedure , neither patients nor investigators were blinded. The primary outcome was pain relief at 1 month and 1 year.
    Detailed Description
    This study will use a randomised controlled trial to access the efficacy and essentiality of the surgery for vertebral compression fractures. Patients aged 50 years or older, had vertebral compression fractures on spine radiograph (minimum 15% height loss) will be invited to take part. Patients will be randomised into 2 arms with average amount. The participants in the intervention arm will have percutaneous vertebroplasty ; those randomised to the control arm will receive current standard conservative treatment methods. Patients were clinically assessed at baseline (the day of surgery or treatment), and at 1 day, 1 week, 1 month, 3 months, 6 months, and 1 year afterwards. The primary outcome will be the pain release , categorised according to WHO classification.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Spinal Fractures
    Keywords
    Spinal Fractures/surgery, Vertebroplasty, Quality-Adjusted Life Years

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    400 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    grade 1
    Arm Type
    Experimental
    Arm Description
    percutaneous vertebroplasty
    Arm Title
    grade 2
    Arm Type
    Active Comparator
    Arm Description
    conservative treatment
    Intervention Type
    Procedure
    Intervention Name(s)
    percutaneous vertebroplasty
    Intervention Description
    Undertake Percutaneous vertebroplasty with polymethylmetacrylate bone cement.
    Intervention Type
    Procedure
    Intervention Name(s)
    conservative treatment
    Intervention Description
    complete on bed with prevention of complications
    Primary Outcome Measure Information:
    Title
    change of pain relief
    Description
    World Health Organization pain classification
    Time Frame
    1 day, 1 week, 1 month, 3 months, 6 months, and 1 year
    Secondary Outcome Measure Information:
    Title
    quality of life
    Description
    Quality of Life Questionnaire of the European Foundation for Osteoporosis (QUALEFFO)
    Time Frame
    1 day, 1 week, 1 month, 3 months, 6 months, and 1 year

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    50 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: vertebral compression fracture on spine radiograph (minimum 15% height loss) level of fracture at Th5 or lower; back pain for 6 weeks or less focal tenderness at fracture level on physical examination bone oedema of vertebral fracture on MRI decreased bone density (T scores ≤-1) Exclusion Criteria: severe cardiopulmonary comorbidity suspected underlying malignant disease radicular syndrome spinal-cord compression syndrome contraindication for radiography exam
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    chen guo
    Phone
    8618055644700
    Email
    fantasy_g@163.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    haiying liu
    Organizational Affiliation
    PekingUPH department of spinal surgery
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Effect and Essentiality of Vertebroplasty Surgery in Acute Vertebral Compression Fractures

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