ClinicalTrials.Veeva

Menu

Outpatient Orthognathic Surgery: "AMBOST" a One Year Study

T

Toulouse University Hospital

Status

Unknown

Conditions

Orthognathic Surgery

Treatments

Procedure: Orthognathic Surgery:

Study type

Observational

Funder types

Other

Identifiers

NCT03486951
2018-A00544-51 (Other Identifier)
RC31/18/0045

Details and patient eligibility

About

The aim of this prospective and observational study is to describe the conditions of orthognathic procedures performed in Toulouse Teaching Hospital over a one-year period, the outpatient-to-inpatient shifts rate and the whole outpatient rate among the whole orthognathic procedures done. The investigator also wants to identify factors associated with an outpatient-to-inpatient shift, and factors associated with the duration of hospitalization.

Full description

In Toulouse Teaching Hospital, the annual number of orthognathic surgery outpatient stays was multiplied by 6 since 2010, indicating a new trend of theses procedures. Outpatient stays presents several advantages for the patient and for the health system: decrease of the psychological stress, higher satisfaction, minimization of the personal and domestic activity interruption, less exposure to nosocomial infections, decrease of global costs, increase of the population rate which can be treated. However, very few data report the experience of outpatient orthognathic surgery in France and the factors associated with its success or failure.

The choice of ambulatory versus complete hospitalization is decided during preoperative consultation by the surgeon in agreement with the patient. The classic surgical and anesthetic protocol of orthognathic surgery is applied whatever the type of hospitalization. The data are collected from the patient medical record (electronic patient record, orthognathic follow-up form, anesthetic sheet) and from a patient quality of life questionnaire. There is no modification of the usual follow-up, patients are seen at D-8 which is the end-study visit.

Enrollment

100 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • all patients treated by an orthognathic surgery in Toulouse Teaching Hospital, having given an oral agreement

Exclusion criteria

  • patient refusal
  • inability to understand the information relative to the procedure, the care and the surgical suites
  • American Society of Anesthesiology (ASA) Score>=3
  • Severe eating disorders
  • Pregnant woman

Trial contacts and locations

1

Loading...

Central trial contact

Frédéric Lauwers, MD; Isabelle Olivier, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems