ClinicalTrials.Veeva

Menu

EPBONF : Evaluation of the Safety and Effectiveness of a Medical Device Aimed at Guiding Orbito-naso-frontal Band Surgery, for the Treatment of Craniostenoses

C

Centre Hospitalier Universitaire de Besancon

Status

Not yet enrolling

Conditions

Craniosynostoses

Treatments

Device: BONFIX system

Study type

Interventional

Funder types

Other

Identifiers

NCT06366178
2024/864

Details and patient eligibility

About

Craniostenosis is a congenital disorder caused by early fusion of the cranial sutures between the skull bones, resulting in orbito-naso-frontal deformities. The damage is primarily aesthetic, but intracranial hypertension may also be observed.

The treatment of craniostenosis involves surgery, to restore harmonious growth between the skull bones and the brain, and proper development of the latter.

There are various surgical techniques for correction, based on remodeling of the upper forehead and the orbito-naso-frontal band (BONF). However, BONF reshaping is difficult to tailor to each individual child. In most cases, the surgeon performs the reshaping "freehand", without a template. The result is therefore subject to the surgeon's experience and judgment.

A surgical instrument (template) has been developed to guide the surgeon in the ideal reshaping of the BONF in patients with anterior craniostenosis (anterior plagiocephaly and trigonocephaly), according to each child's specific morphology.

The aim of EPBONF research is to evaluate the benefits of using this template on the symmetry and angle of the BONF.

Enrollment

5 estimated patients

Sex

All

Ages

4 to 24 months old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Children with anterior craniostenosis (organic trigonocephaly or anterior plagiocephaly), aged 4 to 24 months
  • Procedure performed at Besançon University Hospital
  • Written consent from both parents, or from one parent if there is only one, indicating that they have understood the purpose and procedures of the study, and that they agree to their child's participation in the study and to the study's requirements and restrictions.
  • Affiliation with a French social security scheme or beneficiary of such a scheme.
  • Pre-operative computed tomography scan and cone beam to measure the fronto zygomatic distance and naso-frontal angle in trigonocephaly, and to calculate the frontal process of the zygoma symmetry defect in organic anterior plagiocephaly.

Exclusion criteria

  • Legal incapacity or limited legal capacity of parent(s)
  • Subject is in the exclusion period of another study or is on the "national volunteer list".

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

5 participants in 1 patient group

reshaping the orbito-naso-frontal band with a guide
Experimental group
Treatment:
Device: BONFIX system

Trial contacts and locations

0

Loading...

Central trial contact

Astrid POZET

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems