NCT06771336Recruiting
Biomedical Innovation for Facial Bone Reconstruction in Oncology: BIOFACE PASS a Medico-economic Study Describing the Standard Pathway of Patients Treated by Free Bone Flap
Standard of Care Pathways Evaluation of Patients Treated for Facial Reconstruction After Surgery for Head and Neck Cancer, Using the Conventional Technique (Free Bone Flap): a Medico-economic Study
Source: ClinicalTrials.gov · Last updated 22 Sept 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The purpose of this study is to describe the standard of care pathway of patients treated by free bone flap for facial mandibullar or maxillar reconstruction after surgery for head and neck cancers.
- Status (registry)
- Recruiting
- Study type
- Observational
- Enrollment
- 200 (estimated)
- First submitted
- 7 Jan 2025
- Start date
- 3 Sept 2025
- Primary completion date
- Dec 2029
- Lead sponsor
- University Hospital, Toulouse
- Diseases
- Head and neck cancer
- NCT number
- NCT06771336
What you commit to
- Study type: Observational
- Planned participants: 200
- From 3 Sept 2025 to the primary completion date, Dec 2029
- 9 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Who the study is looking for
- Patient with oral cavity cancer or maxillary and/or oropharynx cancer
- Eligible for treatment by surgery requiring a mandibulectomy or segmental maxillectomy and having a free bone flap for facial reconstruction.
- Patient whose disease is classified Stage cT4a, N0 to N3, M0
- Treatment with a feasible curative aim (no contraindication to optimal treatment such as surgery or chemotherapy at a curative dose)
- Age greater than or equal to 18 years
- Patient affiliated to a Social Security scheme in France
- Patient having given written informed consent
- Non-inclusion Criteria:
- Patient having any situation considered by the doctor as a reason for non-inclusion such as stenosis of the leg tripod not allowing reconstruction by fibula, one or more comorbidity(s) not allowing reconstruction by free bone flap or making this reconstruction too much risk
- Patient having had previous radiotherapy
- Patient with severe coagulation disorders
- Patients deprived of liberty or under legal protection regime (curatorship and guardianship, safeguard of justice)
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (9)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| University hospital of Amiens- Picardie Coordinator of this site? Confirm its status | Amiens | France | Not yet recruiting |
| University Hospital of Lille Coordinator of this site? Confirm its status | Lille | France | Not yet recruiting |
| Hospices Civils de Lyon Coordinator of this site? Confirm its status | Lyon | France | Not yet recruiting |
| University Hospital of Montpellier Coordinator of this site? Confirm its status | Montpellier | France | Not yet recruiting |
| University Hospital of Nantes Coordinator of this site? Confirm its status | Nantes | France | Not yet recruiting |
| Centre Antoine Lacassagne Coordinator of this site? Confirm its status | Nice | France | Not yet recruiting |
| University hospital of Rouen Coordinator of this site? Confirm its status | Rouen | France | Not yet recruiting |
| University Hospital of Toulouse Coordinator of this site? Confirm its status | Toulouse | France | Recruiting |
| Institut Gustave Roussy Coordinator of this site? Confirm its status | Villejuif | France | Not yet recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.