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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03747237
Other study ID # NEU
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 15, 2018
Est. completion date December 31, 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 is to evaluate the correlation between two point distance measurements performed by surgeon on patients face with foldable ruler, which is the most commonly used method, and the subjective scoring will be done by the patient with the help of the edema scale, for measuring edema.


Description:

The patients will be selected among the patients who apply for mandibular impacted third molar extraction to Necmettin Erbakan University, Faculty of Dentistry. A total of 60 patients will be included. All third molar operations will be carried out by the same surgeon in all groups with the same technique.Two methods will be used to evaluate the edema on the face.

1. Method The surgeon will measure from three different places on the patient's face ( two point distance) with the help of a paper ruler.

- Tragus-Pogonion

- Tragus-Labial Komissura

- Angulus Mandibula-Lateral Kantus Measurements will be made preoperative, postoperative 2. and 7. days and saved as milimetre.

2. Method Patients will be given edema scale.With the help of the edema scale, the patients will be evaluated the edema by themselves. When the patient stand in front of the mirror, they will be assessed the edema on their face. And a value between 0 and 4 will be pointed on the scale postoperative 2. and 7. days.

A correlation between the results of the first and second methods will be examined.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date December 31, 2018
Est. primary completion date December 31, 2018
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Impacted mandibular third molar teeth (mesioangular, mucosa and bone retantion)

- Patients with any chronic disease and allergy

Exclusion Criteria:

- Smoking

- Pregnancy or lactation

- pericoronitis

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Edema measurement methods
A correlation between the results of the first and second methods will be examined.

Locations

Country Name City State
Turkey Necmettin Erbakan University, Faculty of Dentistry 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 Tragus-pogonion measurement will be made with paper ruler. The measurement will be done on the 2. and 7. postoperative day and preoperative. Up to 1week
Primary Tragus-labial comissura measurement will be made with paper ruler. The measurement will be done on the 2. and 7. postoperative day and preoperative. Up to 1week
Primary Angulus mandible-latheral cantus will be made with paper ruler The measurement will be done on the 2. and 7. postoperative day and preoperative. Up to 1week
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