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OSA Risk Level in Dental Patients and Correlation With Complications After General Anesthesia

K

Kırıkkale University

Status

Enrolling

Conditions

Postoperative Complications
Obstructive Sleep Apnea of Adult
Dental Caries Under General Anesthesia
Obstructive Sleep Apnea Risk Management

Treatments

Other: The STOP-BANG questionnaire for determining OSA risk level.
Other: ASA recommended criteria for determining OSA risk level.
Other: Record of postoperative complications

Study type

Observational

Funder types

Other

Identifiers

NCT06430957
KU-ERKAN-002

Details and patient eligibility

About

Obstructive sleep apnea (OSA) is a sleep-related respiratory dysfunction. The prevalence of OSA is increasing with the increasing rates of obesity and elderly population worldwide. Perioperative anesthesia management should be adjusted to improve patient safety in patients with OSA. In OSA patients, positive pressure ventilation support may be required in the preoperative period, various ventilation strategies may be required in the intraoperative period, different pharmacologic agents may need to be avoided, and intensive care unit follow-up or noninvasive ventilation support may be required in the postoperative period. However, it is reported that a significant percentage of OSA patients remain undiagnosed. ASA (American Society of Anesthesiologists) has reported the criteria that should be questioned in order to determine the risk of patients in terms of OSA and to initiate the diagnostic process in risky patients and to make appropriate anesthesiologic arrangements in the perioperative period. In addition, the STOP-BANG assessment scale, which is widely used all over the world in OSA risk assessment, is also used in OSA risk assessment. It is thought that dental caries and extraction needs may be higher in OSA patients, especially since open-mouth sleeping accompanies the situation. In this respect, it is also important for patients to be diagnosed with OSA as it may prevent dental damage due to open-mouth sleeping in the future. Identifying patients at risk for OSA and directing them to the diagnostic process is very important for patient safety. Within the scope of the study, the criteria recommended by ASA and STOP-BANG score will be evaluated and recorded. Risk stratification in terms of STOP-BANG questionnaire and ASA criteria will be done separately for each patient and for each classification method. Patients at high risk will be consulted to the relevant medical department in the preoperative period for further investigation and treatment. In addition, it is aimed to correlate the risk levels determined in the study with postoperative respiratory complications and recovery time.

Enrollment

240 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients between 18-80 years of age who apply to the anesthesia clinic for dental procedures planned to be performed under general anesthesia
  • Patients without a previous diagnosis of OSA

Exclusion criteria

  • Individuals who do not want to participate in the study
  • Patients previously diagnosed with OSA
  • Necessity of emergency surgery

Trial design

240 participants in 7 patient groups

Group lowSTOP-B
Description:
Study group including patients in the low-risk group in the assessment to be made with STOP-BANG questionnaire.
Treatment:
Other: Record of postoperative complications
Other: The STOP-BANG questionnaire for determining OSA risk level.
Group intermediateSTOP-B
Description:
Study group including patients in the medium-risk group in the assessment to be made with STOP-BANG questionnaire.
Treatment:
Other: Record of postoperative complications
Other: The STOP-BANG questionnaire for determining OSA risk level.
Group highSTOP-B
Description:
Study group including patients in the high-risk group in the assessment to be made with STOP-BANG questionnaire.
Treatment:
Other: Record of postoperative complications
Other: The STOP-BANG questionnaire for determining OSA risk level.
Group noneASA
Description:
The study group that includes patients who are not at risk for OSA in the evaluation with the criteria recommended by the ASA.
Treatment:
Other: Record of postoperative complications
Other: ASA recommended criteria for determining OSA risk level.
Group mildASA
Description:
Study group including patients in the mild-risk group for OSA in the evaluation with the criteria recommended by the ASA.
Treatment:
Other: Record of postoperative complications
Other: ASA recommended criteria for determining OSA risk level.
Group moderateASA
Description:
Study group including patients in the moderate-risk group for OSA in the evaluation with the criteria recommended by the ASA.
Treatment:
Other: Record of postoperative complications
Other: ASA recommended criteria for determining OSA risk level.
Group severeASA
Description:
Study group including patients in the severe-risk group for OSA in the evaluation with the criteria recommended by the ASA.
Treatment:
Other: Record of postoperative complications
Other: ASA recommended criteria for determining OSA risk level.

Trial contacts and locations

2

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Central trial contact

Gözde Nur Erkan, Asst. Prof.

Data sourced from clinicaltrials.gov

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