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Assessment Study of Faciocraniosynostosis by Craniofacial Osteodistraction

Not Applicable
Completed
Conditions
Faciocraniosynostoses
Interventions
Device: Osteodistraction techniques
Registration Number
NCT01022008
Lead Sponsor
Assistance Publique - Hôpitaux de Paris
Brief Summary

Context. Faciocraniosynostoses present with an insufficient growth of the craniofacial skeleton due to premature fusion of skull and facial sutures. There are prenatal conditions with functional (risk of raised intracranial pressure) and morphological consequences (exorbitism, and impairment of upper respiratory airways), the severity of which justifies an early surgical treatment based on craniofacial osteotomies and osteodistraction techniques.

Distraction techniques were started in our unit eleven years ago, and never ceased to be modified: Recent improvements allowed better correction of exorbitism and therefore reduction of visual risks. But the improvements of the respiratory function remain insufficient. The initial evaluations of the respiratory functions were based on blood oxygenation monitoring, and showed real improvement. But we have routinely screened our patients with complete polysomnography examinations for the past year, and this has always revealed the existence of severe sleep apnea syndromes that we fail to correct completely, although there were slightly improved.

The aim of this PHRC protocol is :

* the qualitative and quantitative improvement of the respiratory status with a reinforced task force group including the specialists in genuine multidisciplinary approach.

* A modification of the surgical technique including modifications of the existing distraction devices, an increased number of implanted devices, and maybe a change in the surgical strategy.

Detailed Description

Study design. This is a monocentric study, the patient being its own control. Due to the extremely low incidence of these conditions, it is foreseen to include twelve patients per year, during two years, which represent 24 patients in total with a minimum follow-up of one year.

Evaluation criteria. The main evaluation criteria are the polysomnography variables (sleep apnea index, characterization of obstructive versus central respiratory events, the oxygenation pattern through the night), which will be performed before and after surgery (6 and 12 months post-op). The secondary criteria are the exorbitism correction analysed with the globe protrusion index and the rate of infections. A multidisciplinary task force group has already been structured in Necker Hospital.

Expected results. We expect to analyze and correct all the sleep apnea syndromes. Many modifications could be made on the distractors, including removal of the activation rods, bioresorbable parts, as well as the modification of the surgical techniques.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
14
Inclusion Criteria
  • age under 18 years
  • faciocraniosynostosis
  • surgery indication to craniofacial osteotomies
  • informed consent
  • social security
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Exclusion Criteria
  • no possibilities of follow-up during one year post-surgery
  • history of radiotherapy
  • acquired or hereditary immunodeficiency syndromes
  • mental retardation
  • bone conditions could not support distractors
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Osteodistraction techniquesOsteodistraction techniquesOsteodistraction techniques
Primary Outcome Measures
NameTimeMethod
Improvement of respiratory function6 months and 1 year
Secondary Outcome Measures
NameTimeMethod
Otorhinolaryngology events6 months and one year
Post-surgery infectionspost surgery

Trial Locations

Locations (1)

Hopital Necker

🇫🇷

Paris, France

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