Trials / Withdrawn
WithdrawnNCT01402167
Evaluating Vertebroplasty and Kyphoplasty for Reducing Trauma-related Fractures
Evaluating Transcutaneous Vertebroplasty and Kyphoplasty for Reducing Trauma-related Fractures: a Randomized Pilot Study Using Catscan Volumetry
- Status
- Withdrawn
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Centre Hospitalier Universitaire de Nīmes · Academic / Other
- Sex
- All
- Age
- 50 Years
- Healthy volunteers
- Not accepted
Summary
The primary objective of this study is to compare the volume of injected ciment (polymethyl methacrylate) between a group of patients treated with vertebroplasty and a group of patients treated via kyphoplasty. Secondary evaluation will compare the restoration of vertebral height, volume and cyphotic angle between the two techniques, as well as extravation of ciment and functional and quality of life aspects related to these techniques.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Kyphoplasty | Patients will be treated via a balloon kyphoplasty surgical procedure |
| PROCEDURE | Vertebroplasty | Patients will be treated via a transcutaneous vertebroplasty procedure. |
Timeline
- Start date
- 2014-09-01
- Primary completion
- 2016-05-01
- Completion
- 2016-08-01
- First posted
- 2011-07-26
- Last updated
- 2015-03-25
Source: ClinicalTrials.gov record NCT01402167. Inclusion in this directory is not an endorsement.