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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03040739
Other study ID # COTYLE_O'ARM
Secondary ID
Status Completed
Phase N/A
First received January 31, 2017
Last updated September 4, 2017
Start date July 8, 2016
Est. completion date June 15, 2017

Study information

Verified date September 2017
Source Groupe Hospitalier Paris Saint Joseph
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Acetabulum fracture are high energy trauma in young people as it can be the result of a simple fall in elder people. This fracture generates an incongruity between acetabulum and femoral head. So surgery is recognized as the best treatment even if technically difficult because of the the complexity of anatomy.Navigation is widely used in orthopaedic surgery .

The aim of the study is to evaluate the effect of peroperative navigation system on reduction of the acetabulum articular surface


Recruitment information / eligibility

Status Completed
Enrollment 56
Est. completion date June 15, 2017
Est. primary completion date January 1, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Age >18 years

- acetabulum fracture dating less than a month

Exclusion Criteria:

- No exclusion criteria

Study Design


Related Conditions & MeSH terms


Intervention

Other:
use of O'ARM imaging system
use of O'ARM imaging system

Locations

Country Name City State
France Groupe Hospitalier Paris Saint Joseph Paris Ile-de-France

Sponsors (1)

Lead Sponsor Collaborator
Groupe Hospitalier Paris Saint Joseph

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Height of incongruity Reduction of the articular surface of the acetabulum Day 1
See also
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Recruiting NCT06365112 - Endoscopic Acetabulum Surgery Early Phase 1