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
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
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
NCT ID
NCT03360383
First Posted
November 25, 2017
Last Updated
December 2, 2017
Sponsor
Peking University People's Hospital
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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