Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07018960

"Multicenter Registry for Chest Wall Reconstruction Using Custom Dynamic Prostheses (PRODIPET)"

Led by Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal · Updated on 2025-08-12

60

Participants Needed

5

Research Sites

91 weeks

Total Duration

On this page

Sponsors

F

Fundacion para la Investigacion Biomedica del Hospital Universitario Ramon y Cajal

Lead Sponsor

H

Hospital Universitario de la Ribera

Collaborating Sponsor

AI-Summary

What this Trial Is About

PRODIPET Study Summary Title: Multicenter Registry for Chest Wall Reconstruction Using Custom 3D-Printed Titanium Prostheses Purpose The PRODIPET study evaluates the safety and effectiveness of personalized, dynamic titanium prostheses for reconstructing the chest wall after: Tumor resection (e.g., sarcomas, lung cancer). Severe trauma (e.g., multiple rib fractures). Traditional methods (metal plates, mesh) often lack flexibility, potentially causing pain or breathing difficulties. This study tests 3D-printed titanium implants designed to mimic natural rib movement, improving function and comfort. Study Design Type: Multicenter, ambispective (retrospective + prospective data). Duration: Prospective: 24 months (Jan 2024-Jan 2026). Follow-up: 12 months per patient (final analysis by 2027). Centers: Major Spanish hospitals (Ramón y Cajal/Madrid, La Ribera/Alzira, Cruces/Baracaldo, Insular/Las Palmas). Key Goals Assess short/mid-term outcomes (pain, breathing, complications). Compare results across patients/surgical techniques. Improve future prosthesis designs. Who Can Participate? Inclusion: Adults (18+) needing chest wall reconstruction. Signed consent for anonymized data sharing. Exclusion: Titanium allergies. Participation in conflicting studies. Patient Experience Pre-Surgery: CT scan creates a custom 3D prosthesis (made by Osteobionix® using Ti6AL4V-ELI titanium). Surgery: Surgeons implant the prosthesis, anchoring it to ribs/sternum. Follow-Up: Evaluations at discharge, 1/6/12 months (in-person or phone). Measures: Pain, lung function, imaging (X-ray/CT), complications (e.g., infection, implant failure). Privacy \& Ethics Data is anonymized and stored securely (REDCap system). Complies with European General Data Protection Regulation (EU GDPR) and Spanish data protection laws. Patients may withdraw anytime. For Healthcare Providers Collaboration: Open to thoracic surgeons/researchers. Data Access: Centralized via REDCap; analyzed by the coordinating team. Publications: Multicenter results will be published first; individual centers may later share their data. Why This Matters Addresses a gap in evidence for dynamic prostheses, which may offer: Better breathing mechanics vs. rigid materials. Fewer long-term complications (e.g., breakage). Could standardize best practices for complex reconstructions. Contact Lead Coordinator: Dr. Nicolás Moreno Mata (Hospital Ramón y Cajal, Madrid). Email: nicolas.moreno.hrc@gmail.com \| Phone: +34 647 609 363. Key Takeaways: Patients/Families: Learn if custom prostheses improve recovery. Providers: Contribute to advancing surgical options. Researchers: Access multicenter data on innovative implants.

CONDITIONS

Official Title

"Multicenter Registry for Chest Wall Reconstruction Using Custom Dynamic Prostheses (PRODIPET)"

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Requires chest wall reconstruction due to oncologic resection (primary tumors, metastases), traumatic injury (flail chest, severe rib fractures), or post-infection/post-radiation defects
  • Chest wall defect involves 2 or more ribs or sternum with instability
  • Defect size is at least 5 cm in largest dimension
  • Scheduled for reconstruction with a custom 3D-printed titanium prosthesis
  • Willing to provide informed consent for surgery, data collection, and follow-up evaluations
Not Eligible

You will not qualify if you...

  • Active systemic infection such as sepsis
  • Severe cardiopulmonary disease with FEV1 less than 30% predicted
  • Uncorrectable blood clotting problems (INR greater than 1.5)
  • Inadequate soft tissue coverage to support the prosthesis
  • Vertebral column involvement requiring complex fixation
  • Known hypersensitivity to titanium alloys
  • Participation in another conflicting clinical trial
  • Inability to complete follow-up evaluations (e.g., no fixed address)
  • Pregnancy due to elective CT scan requirements
  • Prisoners or cognitively impaired patients without legal guardians

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 5 locations

1

Hospital de Cruces

Cruces, Basque Country, Spain

Actively Recruiting

2

Complejo Hospitalario Universitario Insular

Las Palmas de Gran Canaria, Canary Islands, Spain

Actively Recruiting

3

Hospital Universitario Josep Trueta

Barcelona, Catalonia, Spain

Actively Recruiting

4

Hospital Universitario Ramón y Cajal

Madrid, Madrid, Spain

Actively Recruiting

5

Hospital Universitario de La Ribera

Alzira, Valencia, Spain

Actively Recruiting

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Research Team

N

Nicolás Moreno Mata MD, PhD, Medicine

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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