Division of Maxillofacial Surgery, Department of Surgery, AZ Sint-Jan Brugge Oostende AV
Bruges, Belgium
Location status: Recruiting
Location contact
Araceli Diez-Fraile, MSc, PhD, VMD
CONTACT
NCT Number: NCT02762175
Background
Obstructive sleep apnea syndrome (OSAS) is a sleep-related breathing disorder characterized by intense snoring and repetitive complete or partial obstructions of the upper airway during sleep together with daytime sleepiness. Several non-invasive therapeutical options exist, however, they do not offer a permanent improvement. Maxillomandibular advancement (MMA) surgery is a procedure which changes the upper airway in a permanent way.
Objectives
The investigators aim to develop a prospective database registering 3D volumetric changes of the upper airway and its anatomic subregions, the apnea-hypopnea index (AHI) and quality of life (QOL) of all consecutive patients eligible for MMA, performed by Dr. Neyt. Patient demographics, detailed virtual cone-beam computed tomography (CBCT) planning parameters, orthognathic surgery, polysomnographic and QOL data are being collected during consecutive visits within the framework of routine practice.
Design
A prospective, observational cohort study
Study center
General Hospital (AZ) Sint-Jan Brugge-Oostende
Population
The investigators would like to include all OSAS patients (AHI ≥ 5) requiring a MMA by Dr. Neyt starting from January 2015.
Endpoints
The investigators aim to collect data that could provide information about the advantages and disadvantages of the routinely performed 3D CBCT preoperative MMA surgery planning for OSAS patients, regarding 3D volumetric changes of the upper airway and its anatomic subregions and quality of life (QOL) in a subjective manner with the Epworth Sleepiness Scale (ESS) and the OSAS questionnaire and in an objective manner with evaluation of the apnea-hypopnea index (AHI).
Duration
In light of the continuous improvement of patient care, a database will be maintained from January 2015 onwards to enable registration of large-scale OSAS patient data.
Conclusions
Development of a database registering 3D CBCT planning, polysomnographic data and quality of life (QOL) of all consecutive patients eligible for MMA, will provide more information about potential patient, virtual planning and surgical factors influencing accuracy of MMA, and the associated biological benefits of this procedure on the upper airway volume, the AHI and general QOL. Moreover, registration of those results could function as a measurement of quality of care, or could be used for sample size calculation for future large multicenter prospective trials.
Interested in participating?
Request InfoAll sexes
Observational
Bruges, Belgium
Location status: Recruiting
Araceli Diez-Fraile, MSc, PhD, VMD
CONTACT
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 6-12 months
Time frame: 4-6 months
Time frame: 4-12 months
Time frame: 4-12 months
Contact information is provided by the study sponsor or research team.
AZ Sint-Jan AV
Other
3D Volumetric Changes in the Upper Airway After Maxillomandibular Advancement in Obstructive Sleep Apnea Syndrome Patients and the Implication on Quality of Life: A Prospective Registry
Acronym: MMA-OSAS
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07273019
Apnea, Dyssomnias
Bron, France
View Trial DetailsNCT07723144
Apnea, Dyssomnias
Bialystok, Podlaskie Voivodeship, Poland
View Trial DetailsNCT06390345
Apnea, Body Weight
Boise, Idaho, United States
View Trial DetailsNCT05293600
Apnea, Dyssomnias
Boston, Massachusetts, United States
View Trial Details