The Clinical and Radiographic Outcomes of a 3D-printed Patient-specific Biomimetic Bone Substitute in Maxillofacial Indications: an Interventional, Multi-centred, Open-label, Post-market Clinical Investigation.

Bone Regeneration Clinical Trial

Official title:

The Clinical and Radiographic Outcomes of a 3D-printed Patient-specific Biomimetic Bone Substitute in Maxillofacial Indications: an Interventional, Multi-centred, Open-label, Post-market Clinical Investigation.

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT04773847
• Other study ID #: 2020/743
• Status: Not yet recruiting
• Phase: N/A
• Start date: April 2021
• Est. completion date: October 2022

Study information

• Verified date: February 2021
• Source: Mimetis Biomaterials S.L.
• Contact: Emilie Thorel
• Phone: +33672121897
• Email: emilie.thorel[@]mimetis.es
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of the study is to evaluate the clinical and radiographic outcome of MimetikOss 3D as a patient-specific bone substitute in regeneration of osseous defects in several maxillofacial indications. The primary objective is to evaluate the capacity of MimetikOss 3D to perform bone substitute requirements, i.e long-term regeneration of bony tissue in complex defects without detrimental resorption. The secondary main objectives are to assess the versatility of MimetikOss 3D by the variety of maxillofacial sites regenerated and the surgical technique improvement (in terms of surgery duration, blood loss, ease-of-use of the product and surgeon satisfaction).

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 20
• Est. completion date: October 2022
• Est. primary completion date: April 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Male or female age 18 years or over at the time of inclusion into the study;

• Ability to obtain written informed consent from the recipient;

• Patients in need of craniomaxillofacial bone regeneration;

• Ability and capacity to comply with the procedures described in the protocol, including responding to simple questionnaires either by the recipient in person or by a next relative (spouse, parent) who lives with the recipient;

• Patients with good general hygiene;

• Radiographic exam allowing a complete observation of the osseous defect;

• Mimetis approval of the feasibility.

Exclusion Criteria:

• Active tumour;

• Passive tumour with cancer recurrence within 10 years;

• Practice of intensive contact sport exercise during the clinical trial duration;

• Concomitant participation in other clinical trials;

• Women of childbearing potential who are, or plan to become, pregnant during the time of the study;

• Women who are breastfeeding;

• Alcohol or drug abuse as noted in subject records or in subject history;

• Patients with a medical condition that may compromise the healing process or history of systemic diseases that would contraindicate the surgical treatment or any other disease that might have an influence on the involved tissues, such as: severe metabolic disorders, osteogenesis imperfecta, osteoporosis, infectious and degenerative bone diseases, immunodeficiency (congenital or acquired), autoimmune disease, Osler-Weber-Rendu syndrome, unbalanced diabetes, transient hypercalcemia, allergic disposition to phosphate calcium components, titanium or collagen etc; immunosuppressive therapy, steroid therapy, heparin treatment, corticoid treatment, treatments that interfere in the calcium-phosphate metabolism, bisphosphonate intake, Paclitaxel treatment, methotrexate medication etc);

• Acute and chronic infections in the surgery area (e.g. soft tissue infections, inflammatory and bacterial osteopathy, osteomyelitis) and / or mucosal diseases in the areas to be treated;

• In case of intraoral surgery, heavy smokers (>10 cigarettes) excluded;

• Inability to return for follow up visits.

Related Conditions & MeSH terms

• Bone Regeneration

Intervention

Procedure:
• Surgical reconstruction of maxillofacial osseous defect with MimetikOss 3D.
Surgical reconstruction of maxillofacial osseous defect with MimetikOss 3D.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Mimetis Biomaterials S.L.

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Geometric evolution of the grafted volume through radiological evaluation		6 months post-surgery
Secondary	Geometric evolution of the grafted volume through radiological evaluation		12 months post-surgery
Secondary	Versatility of MimetikOss 3D patient-specific bone substitute	MimetikOss 3D can be implanted to regenerate osseous defect from different indications of the maxillofacial area (dental area, jaw and maxilla reconstruction, zygomatic reconstruction and/or chin reconstruction for instance).	12 months post-surgery
Secondary	Incidence of serious adverse events and adverse events		during the surgery / 6 months post-surgery / 12 months post-surgery
Secondary	Bone union observation		12 months post-surgery
Secondary	Surgical technique improvement in terms of accuracy of MimetikOss 3D design and positioning		directly after the surgery / 6 months post-surgery / 12 months post-surgery
Secondary	Surgical technique improvement in terms of total surgery duration and duration of implantation of MimetikOss 3D		during the surgery
Secondary	Surgical technique improvement in terms of blood loss measurement		during the surgery
Secondary	Surgical technique improvement in terms of surgeon satisfaction		12 months post-surgery
Secondary	Aesthetic evaluation by visual observation of the symmetry of the face, pictures and/or irregular contours prosthetic palpable (if applicable)		directly after the surgery / 6 months post-surgery / 12 months post-surgery