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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01544933
Other study ID # rtisot01
Secondary ID
Status Completed
Phase N/A
First received February 22, 2012
Last updated March 5, 2012
Start date February 2011
Est. completion date September 2011

Study information

Verified date August 2011
Source Universidade de Passo Fundo
Contact n/a
Is FDA regulated No
Health authority Brazil: Ethics Committee of University of Passo Fundo
Study type Observational

Clinical Trial Summary

The purpose of this study is to analyse the anatomic influence of the ribs related to the incidence and severity of burst spine fractures.


Description:

To analyse the anatomic influence of the ribs related to the incidence and severity of burst spine fractures, with the measurements of kyphosis, vertebral collapse and vertebral canal narrowing


Recruitment information / eligibility

Status Completed
Enrollment 2
Est. completion date September 2011
Est. primary completion date August 2011
Accepts healthy volunteers No
Gender Both
Age group 17 Years to 79 Years
Eligibility Inclusion Criteria:

- burst fractures in thoracic spine

Exclusion Criteria:

- fractures that were not burst fractures in thoracic spine

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Locations

Country Name City State
Brazil Rodrigo Tisot Passo Fundo RS

Sponsors (1)

Lead Sponsor Collaborator
Universidade de Passo Fundo

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary residual kyphosis measurement of residual kyphosis by x-ray 3 years Yes
Secondary vertebral canal narrowing vertebral canal narrowing in CT 3 years Yes