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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04207515
Other study ID # 2018/24
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date April 15, 2018
Est. completion date September 20, 2019

Study information

Verified date April 2018
Source University of Beykent
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The specific aims of the present study were to evaluate sAA responses to impacted third molar extractions at different time points in the patients under conscious sedation with local anesthesia and to examine the relationship between sAA, conscious sedation and dental anxiety. The null hypothesis was that conscious sedation could be considered to reduce salivary alpha amylase level during the wisdom tooth surgery.


Description:

In oral and maxillofacial surgery, surgical extraction of impacted third molars is one of the most common surgical techniques performed in the oral cavity. Conscious intravenous sedation could be administered for the patients to provide anxiolysis, sedation, and analgesia for the patient. Salivary alpha-amylase (sAA) which reflect stress-related changes in the autonomic nervous system (ANS), has been proposed as a non-invasive stress biomarker. The aim of the present study was to investigate whether salivary alpha amylase (sAA) levels could be decreased by conscious sedation in the patients undergoing impacted third molar extraction. A total of 18 male patients were recruited. All patients were administered Modified Dental Anxiety Scale (MDAS) test. Patients were divided into two groups: test group (procedures under sedation) and control group (procedures under local anesthesia). The following parameters were monitored at different study time-points: systolic blood pressure (SBP), diastolic blood pressure (DBP), oxygen saturation (SO2), and heart rate (HR). Five samples of saliva were taken from each patient: the first time patient came to clinic, the patient sat in the chair for extraction, before local anesthesia, immediately after extraction, at 4 h after extraction. The concentrations of sAA were measured and compared across the different stages of the study between two groups.


Recruitment information / eligibility

Status Completed
Enrollment 20
Est. completion date September 20, 2019
Est. primary completion date June 15, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Male
Age group 19 Years to 33 Years
Eligibility Inclusion Criteria:

- Man

- 18-35 years

- individuals without chemotherapy or radiotherapy history

- individuals without antibiotics and NSAIDs history in the last month

- individuals without any medications that affect saliva content in the last 1 month

- individuals without corticosteroid treatment history

- nonsmokers

- wisdom tooth which is indicated to extract

- individuals without acute infectious lesion in the mouth

- individuals without alcohol or substance abuse

- individuals without inflammatory bone disease

Exclusion Criteria:

- Woman

- individuals with any systemic disorders

- individuals with chemotherapy and radiotherapy history

- individuals with antibiotics and NSAIDs history in the last month

- individuals with use of antibiotics and NSAIDs history in the last month

- individuals with corticosteroid treatment history

- Smokers

- individuals with acute infectious lesion in the mouth

- individuals with inflammatory bone disease

- individuals with alcohol or substance abuse

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Procedures of wisdom tooth removal surgery under conscious sedation
The first specimen of saliva was taken at the first time patient came to clinic (t1). Saliva was allowed to flow in the floor of mouth an 1 ml was then collected using a Pasteur pipette. First day after examination, patient was given an appointment. The second time of the saliva was taken was when the patient sat in the chair for extraction (t2). The other times of saliva samples were taken were before local anesthesia (t3), immediately after extraction (t4) and at 4 h after extraction (t5). Due to the localization and position of the third molar, osteotomy was performed using a 20,000-rpm hand piece under irrigation for all patients. Some cases required tooth sectioning. 3-0 silk suture was used at the end of the surgery.
Procedures of wisdom tooth removal surgery under local anesthesia
The first specimen of saliva was taken at the first time patient came to clinic (t1). Saliva was allowed to flow in the floor of mouth an 1 ml was then collected using a Pasteur pipette. First day after examination, patient was given an appointment. The second time of the saliva was taken was when the patient sat in the chair for extraction (t2). The other times of saliva samples were taken were before local anesthesia (t3), immediately after extraction (t4) and at 4 h after extraction (t5). Due to the localization and position of the third molar, osteotomy was performed using a 20,000-rpm hand piece under irrigation for all patients. Some cases required tooth sectioning. 3-0 silk suture was used at the end of the surgery.

Locations

Country Name City State
Turkey Selin Gas Beylikduzu

Sponsors (1)

Lead Sponsor Collaborator
University of Beykent

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Salivary Alpha Amylase Level The measurement of salivary alpha amylase levels (t1. The first time the patient came to clinic, t2. When the patient sat in the chair for extraction, t3. Before local anesthesia, t4. Immediately after extraction, t5. 4 h after extraction) Change from baseline salivary alpha-amylase levels at different time points in one day
Secondary Systolic blood pressure (SBP) level The measurement of Systolic blood pressure level at different time points (preoperative time; intraoperative time-after local anesthesia, intraoperative time-after extraction, postoperative time) Change from baseline systolic blood pressure levels at different time points in one day
Secondary Diastolic blood pressure (DBP) level, Diastolic blood pressure level at different time points (preoperative time; intraoperative time-after local anesthesia, intraoperative time-after extraction, postoperative time) Change from baseline diastolic blood pressure levels at different time points in one day
Secondary Oxygen saturation (SO2) level Oxygen saturation (SO2) level at different time points (preoperative time; intraoperative time-after local anesthesia, intraoperative time-after extraction, postoperative time) Change from baseline oxygen saturation levels at different time points in one day
Secondary Heart rate (HR) level Heart rate (HT) level at different time points (preoperative time; intraoperative time-after local anesthesia, intraoperative time-after extraction, postoperative time) Change from baseline heart rate levels at different time points in one day
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