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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04618991
Other study ID # APHP201080
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date March 15, 2021
Est. completion date April 15, 2024

Study information

Verified date October 2022
Source Assistance Publique - Hôpitaux de Paris
Contact Boris Petelle, MD
Phone 0033 6 62 40 01 50
Email boris.petelle@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The research aims to assess the impact on quality of life of surgically maxillary expansion in adult patients followed for obstructive sleep apnea syndrome.


Description:

This assessment will be done using the following elements: - The score of the Quebec sleep questionnaire (QSQ), developed in 2004 by Lacasse Y. et al. This questionnaire is specific to sleep apnea and may be self-administered. The main interest of this questionnaire is to measure the change in quality of life over time. - The Epworth Scale Score, developed in 1991 by Murray W. John. This is a self-administered questionnaire developed to measure daytime sleepiness. - Gender, age group, BMI - The radiological assessment - The results of polysomnography Patients will be followed for a period of 1 year and one month after surgery. The protocol visits correspond to the rhythm of post-surgery follow-up consultations in current practice. These patients are followed by Dr. Pételle at Saint-Antoine Hospital. During these visits, they will complete the Quebec sleep questionnaire and the Epworth scale, at baseline, at 3 months and then at 1 year.


Recruitment information / eligibility

Status Recruiting
Enrollment 10
Est. completion date April 15, 2024
Est. primary completion date April 15, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult patients - With obstructive sleep apnea confirmed by polysomnography - Surgical indication for surgically maxillary expansion Exclusion Criteria: - - Patients refusing to participate in the survey having formulated their opposition - Diabetes, - Obesity (BMI> 30) - Failure to provide informed written consent - Refusal or inability to return to all follow-up visits and sleep studies - Patient pregnant or planning to become pregnant in the next 12 months or breastfeeding - Surgical resection or radiation therapy for cancer or congenital malformations of the larynx, tongue or throat (Note that some previous surgeries, such as uvulopalatopharyngoplasty (UPPP), tonsillectomy or adenoidectomy, to remove obstructions related to obstructive sleep apnea are allowed) - Obvious obstructions of the fixed upper airways (tumors, polyps or nasal obstruction) - Patients who have undergone previous surgery on the mandible and / or maxilla, other than dental treatment. - Patients included in another clinical study (excluding registers). - Patients taking medicines such as opiates which may affect sleep, alertness or breathing

Study Design


Intervention

Other:
Filling the Quebec Sleep Questionnaire
Filling the Quebec Sleep Questionnaire (QSQ) by the pre-surgery patient, then at 3 months post surgery and 1 year post surgery.

Locations

Country Name City State
France Service d'ORL, Hôpital Saint Antoine Paris

Sponsors (1)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Score of the QSQ Score of the QSQ filled directly by the patient before surgery, compared to that then 3 months after surgery. at 3 months
Secondary Score of the Quebec Sleep Questionnaire (QSQ) Score of the QSQ filled directly by the patient before surgery, compared to that then 1 year after surgery. at 1 year
Secondary Polysomnography Search for a modification of the polysomnography data before and after surgery at 3 months
Secondary Epworth scale Epworth scale score changes before and after surgery at 1 year
Secondary correlation between the results of the Quebec Sleep Questionnaire (QSQ) score and the anthropometric data correlation between the results of the QSQ score and the anthropometric data at 1 year
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