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Vertebroplasty Using Real-Time, Fluoroscopy-Controlled, Catheter-Assisted, Low-Viscosity Cement Injection

The recruitment status of this study is unknown. The completion date has passed and the status has not been verified in more than two years.
Verified May 2008 by National Taiwan University Hospital.
Recruitment status was:  Active, not recruiting
Sponsor:
ClinicalTrials.gov Identifier:
NCT00689923
First Posted: June 4, 2008
Last Update Posted: June 4, 2008
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
National Taiwan University Hospital
June 1, 2008
June 4, 2008
June 4, 2008
November 2007
October 2008   (Final data collection date for primary outcome measure)
pain relief [ Time Frame: immediately after procedure ]
Same as current
No Changes Posted
cement leak [ Time Frame: immediate after procedure ]
Same as current
Not Provided
Not Provided
 
Vertebroplasty Using Real-Time, Fluoroscopy-Controlled, Catheter-Assisted, Low-Viscosity Cement Injection
Vertebroplasty Using Real-Time, Fluoroscopy-Controlled, Catheter-Assisted, Low-Viscosity Cement Injection
Th low viscosity cement injection is safe in vertebroplasty procedure with Comparacle out come in pain relief.

Pain relief; Comparatle

Cement Leakage; Comparacle

Irradiation dose:less

Observational
Observational Model: Case-Only
Time Perspective: Prospective
Not Provided
Not Provided
Non-Probability Sample
painful vertebral compression fracture
  • Osteoporosis
  • Compression Fracture
Not Provided
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Unknown status
100
Not Provided
October 2008   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • all painful fracture that can not be relieved by pain killer.

Exclusion Criteria:

  • infection and malignancy in local region
Sexes Eligible for Study: All
45 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Not Provided
 
 
NCT00689923
200710029R
200710029R
No
Not Provided
Not Provided
National Taiwan University Hospital
National Taiwan University Hospital
Not Provided
Not Provided
National Taiwan University Hospital
May 2008