Treatment of Acetabular Fracture: the Contribution of the 3D Impression
Sponsor
Groupe Hospitalier Paris Saint Joseph (Other)
Overall Status
Completed
CT.gov ID
NCT03312491
Collaborator
(none)
30
1
4.3
7
Study Details
Study Description
Brief Summary
Acetabular fracture are common in elder patients and high energy trauma in younger one.
However, the fracture deplacement induces incongruity between cotyloid cavity and femoral head. Anatomic reduction and osteosynthesis of these fracture are technically difficult .
3D printing ease the process of operating planification or implant fabrication. The 3D impression allows to obtain a model on the scale of the pond of the patient allowing to pre mold plates on the anatomy of the patient before he is operated with the aim of decreasing the surgical time and improving the quality of the reduction.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Study Design
Study Type:
Observational
Actual Enrollment
:
30 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Treatment of Acetabular Fracture: the Contribution of the 3D Impression
Actual Study Start Date
:
Aug 22, 2016
Actual Primary Completion Date
:
Dec 31, 2016
Actual Study Completion Date
:
Dec 31, 2016
Outcome Measures
Primary Outcome Measures
- operating room time [day1]
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Inclusion Criteria:
-
age >18
-
acetabulum fracture within one month
-
anterior access or double access
Exclusion Criteria:
- acetabulum fracture more than one month
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Groupe Hospitalier Paris Saint Joseph | Paris | Ile-de-France | France | 75014 |
Sponsors and Collaborators
- Groupe Hospitalier Paris Saint Joseph
Investigators
- Study Chair: Pomme JOUFFROY, MD, GHPSJ
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
Groupe Hospitalier Paris Saint Joseph
ClinicalTrials.gov Identifier:
NCT03312491
Other Study ID Numbers:
- 3D COTYLE
First Posted:
Oct 17, 2017
Last Update Posted:
Oct 17, 2017
Last Verified:
Oct 1, 2017
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms: