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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05890040
Other study ID # 021/12-08
Secondary ID
Status Active, not recruiting
Phase
First received
Last updated
Start date July 8, 2021
Est. completion date July 8, 2023

Study information

Verified date May 2023
Source Kutahya Health Sciences University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Surgical extraction of impacted wisdom teeth creates a high level of anxiety on patients. Anxiety in patients can affect the difficulty of tooth extraction, prolong the duration of surgery and increase post-operative pain. With the increasing internet usage in recent years; patients can access different information about surgical procedures by watching videos on various social media platforms in an uncontrolled manner. In the literature, the effects of impacted tooth extraction videos, which are watched by physicians before the operation, on anxiety have been examined. However, studies on the evaluation of the effect of the surgery videos watched by the patients before the surgery on their own will on anxiety and pain perception have been limited.


Description:

The study is given to KSBU Faculty of Dentistry, Department of Oral, Dental and Maxillofacial Surgery; It will be applied to patients who are referred from Oral, Dental and Maxillofacial Radiology and who want to participate in the study. In our study, the Situational-Trait Anxiety Inventory will be used to assess anxiety. Patients who are referred to our clinic from Oral, Dental and Maxillofacial Radiology and who have impacted wisdom teeth will be evaluated in terms of extraction indication. Patients with indications for extraction will be asked to rate the sentences in the State and Trait Anxiety Inventory when making an appointment. Patients will be informed about impacted tooth extraction as it is routinely practiced. Within the scope of this study, no information about the extraction will be given in the Oral, Dental and Maxillofacial Radiology clinic, standard information will be given to the patients in our clinic and the surgery appointment will be given one week later. On the day of tooth extraction, patients will be asked whether they watched a video about impacted tooth extraction from any social media platform. The patients who watch the video will be assigned to the study group, and the patients who do not watch the video will be assigned to the control group, so the study will be conducted over two groups. If the patient has watched the video; He will be asked whether he watches an animation video or a video with real surgery footage, and the reason for watching the video. Then, before starting the operation, they will be asked to score the sentences in the Situational and Trait Anxiety Inventory. By comparing the Situational Anxiety Inventory made at the time of the surgery appointment with the Situational Anxiety Inventory scores made just before the surgery, it will be evaluated whether the patients who watch videos have more anxiety. At the same time, it will be evaluated whether the patients who have a high Trait Anxiety Inventory score when making an appointment and who generally have high anxiety watch more videos. This study is planned to be performed on a total of 60 patients, 30 of whom watch videos and 30 who do not.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 60
Est. completion date July 8, 2023
Est. primary completion date July 8, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Patients between the ages of 18-45 - The patient does not have any systemic disease. - Patients with mesio-angular or 2 or 3 / B according to the Pell and Gregory classification of the impacted tooth radiographic grade according to Winter classification Exclusion Criteria: - Patients using antidepressant and anxiolytic drugs - Patients with a history of impacted tooth extraction/difficult tooth extraction - Patients with systemic disease - Female patients who are pregnant or breastfeeding

Study Design


Related Conditions & MeSH terms


Intervention

Other:
questionnaire
assessment of anxiety

Locations

Country Name City State
Turkey Kutahya University of Health Sciences Kütahya Merkez

Sponsors (1)

Lead Sponsor Collaborator
Kutahya Health Sciences University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluation of anxiety in impacted wisdom tooth extraction State and trait anxiety inventory( STAI-T and STAI-S) one week before impacted tooth extraction
Primary Evaluation of anxiety in impacted wisdom tooth extraction State and trait anxiety inventory( STAI-T and STAI-S) just before impacted tooth extraction
See also
  Status Clinical Trial Phase
Active, not recruiting NCT02133326 - Efficacy Study of IV Ibuprofen vs IV Acetaminophen Post Surgical Extraction Phase 2