Deep Sedation Clinical Trial
Official title:
Comparison of Nasal Continuous Positive Airway Pressure (CPAP) Mask and Nasal Airway in Terms of Intraoperative Anesthesia Quality and Postoperative Associated Complications in Impacted Molar Tooth Extraction Patients Under Deep Sedation; A Multi-Center Study
In patients with high levels of fear and anxiety, it is recommended to perform dental procedures under sedation or general anesthesia depending on the nature of the procedure. In dental treatment under anesthesia, it is important that the procedure is comfortable and well tolerated by the patient. In addition, patient comfort is important in all dental procedures to prevent the development of avoidance behavior. During dental procedures performed under anesthesia, the oral cavity is completely within the scope of the surgical or procedure field. In this respect, sedation and general anesthesia in dental procedures and operations have specific risks and challenges.Since there is a risk of respiratory depression, hypoxia and hypercarbia during deep sedation, non-invasive ventilation support provided to patients with airway devices would be beneficial. In the research clinics where the study will be conducted, deep sedation with non-invasive mechanical ventilation support using a nasal CPAP (Continuous Positive Airway Pressure) mask or nasal airway is applied during the extraction of impacted molars. Thus, many dental procedures are routinely performed under deep sedation without the need for general anesthesia. There are very limited data in the literature on the use of a nasal CPAP mask during sedation for different procedures in patients with obstructive sleep apnea or obesity. However, no study comparing ventilation support during deep sedation with nasal CPAP mask and nasal airway has been found in the literature. The aim of this study is to compare the non-invasive ventilation support provided with 2 different airway devices during the procedure in terms of intraoperative and postoperative related complications, ventilation parameters, patient and surgeon satisfaction. The hypothesis of the study is that two different ventilation support methods during deep sedation may be superior to each other in terms of anesthesia quality, postoperative complications related to airway devices, patient and surgeon satisfaction. In the study, a total of 60 patients (Group airway, n;30, Group Mask, n;30) from 2 centers are planned to be included in the study by performing power analysis with a statistical power of the trial >0.8. The permutation method will be applied within the scope of the restricted randomization method to determine the group of patients to be included.
Status | Not yet recruiting |
Enrollment | 60 |
Est. completion date | June 3, 2025 |
Est. primary completion date | April 3, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - Volunteer adult patients aged 18-60 years - Patients scheduled for impacted tooth extraction - Cases with surgical time =20 minutes and =60 minutes - American Society of Anaesthesiologists (ASA) physical status I and II patients - Patients with BMI=30 Exclusion Criteria: - Patients under 18 years old-over 60 years old - Surgeries with a procedure time over 1 hour or less than 20 minutes - American Society of Anaesthesiologists (ASA) physical status III and higher patients - Presence of conditions such as mental retardation that impair the patient's ability to make decisions about himself/herself - Patients with respiratory system diseases such as asthma, chronic obstructive pulmonary disease (COPD) or airway hyperreactivity - Patients with a condition that severely narrows the nasal passage opening (e.g. adenoid hypertrophy, etc.) - Patients with BMI>30 - Patients who refused to participate in the study |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Gözde Nur Erkan | Kirikkale University, TC Erciyes University |
Appukuttan DP. Strategies to manage patients with dental anxiety and dental phobia: literature review. Clin Cosmet Investig Dent. 2016 Mar 10;8:35-50. doi: 10.2147/CCIDE.S63626. eCollection 2016. — View Citation
Bai Y, Xu Z, Chandrashekar M, St Jacques PJ, Liang Y, Jiang Y, Kla K. Comparison of a simplified nasal continuous positive airways pressure device with nasal cannula in obese patients undergoing colonoscopy during deep sedation: A randomised clinical trial. Eur J Anaesthesiol. 2019 Sep;36(9):633-640. doi: 10.1097/EJA.0000000000001052. — View Citation
Cukierman DS, Perez M, Guerra-Londono JJ, Carlson R, Hagan K, Ghebremichael S, Hagberg C, Ge PS, Raju GS, Rhim A, Cata JP. Nasal continuous positive pressure versus simple face mask oxygenation for adult obese and obstructive sleep apnea patients undergoing colonoscopy under propofol-based general anesthesia without tracheal intubation: A randomized controlled trial. J Clin Anesth. 2023 Oct;89:111196. doi: 10.1016/j.jclinane.2023.111196. Epub 2023 Jul 3. Erratum In: J Clin Anesth. 2023 Nov 20;:111346. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Non-invasive blood pressure | It is planned to record non-invasive blood pressure values of the patients at regular intervals during the operation, recovery unit and inpatient ward follow-up. Changes in blood pressure above 20% from baseline will be recorded additionally. | Intraoperative period and for 4 hours after surgery | |
Primary | ECG | It is planned to record heart rate values of the patients at regular intervals during the operation, recovery unit and inpatient ward follow-up. Changes in heart rate greater than 20% of baseline will be recorded additionally. | Intraoperative period and for 4 hours after surgery | |
Primary | Peripheral oxygen saturation | It is planned to record peripheral oxygen saturation values of the patients at regular intervals during the operation, recovery unit and inpatient ward follow-up. Hypoxia (SpO2<90%) will be recorded additionally. | Intraoperative period and for 4 hours after surgery | |
Primary | Respiratory rate | It is planned to record respiratory rate values of the patients at regular intervals during the operation, recovery unit and inpatient ward follow-up. Respiratory depression will be recorded additionally. | Intraoperative period and for 4 hours after surgery | |
Primary | Number of interruptions for an anesthesia-related reason | Number of episodes during deep sedation when the procedure has to be interrupted due to desaturation or patient movement will be recorded | Intraoperative period | |
Primary | Tidal volume | During non-invasive ventilatory support, set and actual tidal volume values will be recorded at regular intervals during the operation. | Intraoperative period | |
Primary | Peak pressure | During non-invasive ventilatory support, peak pressure values will be recorded at regular intervals during the operation. | Intraoperative period | |
Primary | End tidal carbon dioxide level (EtCO2) | During non-invasive ventilatory support, end tidal carbon dioxide values will be recorded at regular intervals during the operation. | Intraoperative period | |
Primary | Minute ventilation | During non-invasive ventilatory support, minute ventilation values will be recorded. | Intraoperative period | |
Secondary | Postoperative complications related non-invasive ventilation support devices and sedation | During the recovery unit and inpatient ward follow-up, patients will be monitored for the presence of nausea/vomiting, pain and/or itching/dryness in the nose and/or throat. A 10-point Likert scale would be used for nausea and vomiting assessment (0 points: No nausea, 1-2 points: Very mild nausea, 3-4 points: Mild nausea, 5-6 points: Moderate nausea, 7-8 points: Severe nausea and 9-10 points: worst nausea). For pain, a 10-point visual analog scale would be used. Additionally, the development of epistaxis will be recorded. | During the next 3 hours after the end of the operation | |
Secondary | Patient and surgeon satisfaction | Using a 5-point Likert scale, the satisfaction level of the patients and the surgeon will be questioned and recorded. In the Likert scale, 5 indicates the highest level of satisfaction and 1 indicates the lowest level of satisfaction. | Perioperative period | |
Secondary | Total dose of medications used for sedation during the procedure | The total dose of anesthetic medications required to provide a depth of sedation with a Ramsey sedation score of 5 or higher during the surgical procedure will be recorded | Intraoperative period | |
Secondary | Recovery duration from anesthesia | The time until the Modified Aldrete Score is 9 or higher during the recovery period | From the end of the operation until discharge to the ward |
Status | Clinical Trial | Phase | |
---|---|---|---|
Terminated |
NCT03781817 -
Intranasal Versus Intravenous Ketamine for Procedural Sedation in Children With Non-operative Fractures
|
Phase 4 | |
Recruiting |
NCT05539521 -
Efficacy and Safety of Remimazolam Besylate Versus Propofol for Sedation in Critically Ill Patients With Deep Sedation
|
Phase 2 | |
Completed |
NCT01170156 -
Fluid Leakage Past Tracheal Tube Cuff : Effect of Suctioning Manoeuvre
|
N/A | |
Terminated |
NCT02903407 -
Pain, Agitation and Delirium (PAD) Protocol in the Duke CICU
|
Phase 4 | |
Completed |
NCT04695509 -
Sedation and Neuromediators Concentration
|
N/A | |
Not yet recruiting |
NCT03687385 -
The Effect of High-flow Nasal Oxygenation to the Saturation During Analgo-sedation in Different ASA Risk Class Patients
|
N/A | |
Not yet recruiting |
NCT03687424 -
Can High-flow Nasal Oxygenation Improve Oxygen Saturation During Analgo-sedation in Obese Adults?
|
N/A | |
Completed |
NCT02302391 -
Pharmacokinetic Analysis of Midazolam and Fentanyl in Pediatric Patients With Long-term Analgosedation
|
||
Recruiting |
NCT03893877 -
Comparison of Oxygenation Methods in Sedation
|
N/A | |
Completed |
NCT00639548 -
ERPS, BIS and Entropy for Neuromonitoring in ICU Patients
|
N/A | |
Terminated |
NCT04168294 -
The Influence of Sedation for Endoscopy on Cognitive Function
|
||
Withdrawn |
NCT04026451 -
Spectral Edge Frequency From Spectral EEG Analysis to Guide Deep Sedation in the Critical Care Setting (Pilot)
|
N/A | |
Completed |
NCT05163704 -
Dexmedetomidine Sedation in Children Before MRI Examinations
|
N/A | |
Completed |
NCT05587803 -
Comparison of 2 Depth of Sedation Indices in the Intensive Care Unit
|
N/A | |
Completed |
NCT04141267 -
Inhaled Sedation Using the Anesthetic-conserving Device ( ANACONDA) in Prehospital Emergency Medecine.
|
||
Active, not recruiting |
NCT02909010 -
Bispectral Index Monitoring To Guide Sedation In The Critical Care Setting
|
N/A | |
Completed |
NCT03652324 -
What Should be the Anesthesia Method in Endobronchial Coil Treatment
|
N/A | |
Completed |
NCT00717574 -
Addition of Nitrous Oxide and Its Effects on Depth of Anesthesia
|
N/A | |
Completed |
NCT00641563 -
Effects of Two Different Sedation Regimes on Auditory Evoked Potentials and Electroencephalogram (EEG)
|
N/A | |
Completed |
NCT05674201 -
Effects Of Propofol-Dexmedetomıdıne And Propofol- Remıfentanıl In Hysteroscopıc Operations.
|