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Clinical Trial Summary

The investigators want to analyse the advantages of using a 3D constructed prototype from a previous CT Scan to model an external customised guide por percutaneous Scaphoid fixation.

The investigators hypothesise that the usage of this device will shorten surgery time, radiation for the surgery team and optimise the percutaneous screw trajectory inside of the scaphoid bone.


Clinical Trial Description

To carry out this analysis the investigators will recruit 10 patients who present with an acute fracture of the Scaphoid bone type B1 and B2 (Herbert Classification).

A CT Scan will be performed and a 3D exoesqueleton model printed, previously deciding the position of the fixation screw inside of the bone and adding a cannulated sleeve in the volar aspect of the exoesqueleton to insert the initial positional guide wire for surgery.

Surgery time, surgery radiation exposure and screw positioning will be recorded and compared to 10 control patients operated following standard procedure. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03502720
Study type Observational [Patient Registry]
Source Corporacion Parc Tauli
Contact Francesc A Marcano Fernandez, MD
Phone (34) 618023575
Email francescmarcano@gmail.com
Status Recruiting
Phase
Start date March 25, 2018
Completion date March 29, 2019