RecruitingNot ApplicableNCT06603831

Clinical Evaluation and Cost-effectiveness Analysis of 3D Digital Surgery in Traumatology

Randomized, Prospective and Multicenter Clinical Study for the Clinical Evaluation and Cost-effectiveness Analysis of 3D Digital Surgery in Traumatology and Orthopedic Surgery


Sponsor

Corporacion Parc Tauli

Enrollment

180 participants

Start Date

Oct 21, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Digital surgery, in combination with patient specific instrumentation (PSI) is being used more and more in traumatology due to its proven benefits and applications. Nowadays, medical case planning and an optimal preparation before surgery are still a challenge for surgeons. This lack of preparation is translated into longer surgical procedures, potential complications, unnecessary sterilization of materials and a high number of fluoroscopies. 2D techniques such as Magnetic Resonance Imaging (MRI), Computed Tomography (CT) and X-rays remain essential for medical planning, however, in many cases, a 3D visualization is needed to achieve better results, especially in complex cases.The use of personalized medical instruments such as surgical guides has proven to increase clinical accuracy, assuring a better correction of bone deformities, and allowing a more precise location of implants and screw positioning. Furthermore, the use of 3D-printed patient-specific prosthesis can lead to better clinical outcomes as they reduce the number of complications as well as they present a longer lifespan compared to conventional generic implants.Despite the potential of 3D technology in the medical field, there is still a lack of robust studies that compares clinical benefits between digital surgery and conventional 2D surgery, and its economic impact is still unknown. Thus, the investigators propose this randomized, prospective and multi-center clinical study to evaluate the use of 3D technology in traumatology. The aim of this project is to prove that digital surgery is a cost-effective methodology and therefore it should be adopted by the public health system as a gold standard procedure.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Inclusion Criteria2

  • \- Patients that requires one of the following surgical procedures / interventions: Radius osteotomy due to non-articular metaphyseal malunion Complex acetabular arthroplasty Thoracic-lumbar spine arthrodesis.
  • Patients that can understand the clinical study and that are able to read, understand and sign the consent form

Exclusion Criteria3

  • Patients that are not able to read, understand or sign the consent form.
  • Patients that can't or have no support to complete the clinical trial.
  • Patients with complex deformities or complications that would require mandatory personalized digital surgery treatment

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Interventions

PROCEDUREpatients treated using 3D technology and Patient-Specific Instrumentation

3D Digital surgery includes: * 3D Surgical Planning using biomedical engineering software; 3D visualization of the patients anatomy and surgical simulation. * Use of personalized surgical guides created through additive manufacturing. * Use of personalized implants created through additive manufacturing. 3 surgical procedures are studied in this study; radius osteotomy, acetabular arthroplasty and spinal arthrodesis

PROCEDUREPatients treated with conventional surgery, without using 3D technology

Conventional surgery includes: * 2D planning using TC and x-rays * Free-hand surgery * Use of generic, non-personalized implants 3 surgical procedures are studied in this study; radius osteotomy, acetabular arthroplasty and spinal arthrodesis


Locations(1)

Hospital Parc Taulí

Sabadell, Barcelona, Spain

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NCT06603831


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