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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03752255
Other study ID # NEU2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 21, 2018
Est. completion date December 21, 2018

Study information

Verified date November 2018
Source Konya Necmettin Erbakan Üniversitesi
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study was to evaluate preoperative anxiety levels using dental anxiety scale (DAS) and the Spielberger State-Trait Anxiety Inventory (STAI).


Description:

This study will based on a prospective, observational investigation of two different patient education techniques about the effect of third molar removal on patients' anxiety level. A total of 240 patients will be divided into two groups.

Information about operation procedures and a recovery will be given verbally in group 1 and information about operation procedures and recovery will be given in group 2. Anxiety levels were assessed by using DAS and (STAI).Paired t-test or Wilcoxon test will be used for intra-group comparison of anxiety levels.


Recruitment information / eligibility

Status Completed
Enrollment 240
Est. completion date December 21, 2018
Est. primary completion date December 21, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Impacted third molar (bone and mucosa retention, mesioangular position)

- Patients with any chronic disease and allergy

Exclusion Criteria:

- Pericoronitis

- Patients with visual impairment

- Patients with psychological disorders

- Smoking

- Pregnancy or lactation

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Anxiety measurement method
Two different techniques (video or verbal information) will be examined about impacted third molar surgery.

Locations

Country Name City State
Turkey Necmettin Erbakan University Konya Karatay

Sponsors (1)

Lead Sponsor Collaborator
Konya Necmettin Erbakan Üniversitesi

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary The anxiety levels will be examined using DAS and STAI. first day first day
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