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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03261869
Other study ID # D-KA 15/07
Secondary ID
Status Completed
Phase N/A
First received August 23, 2017
Last updated August 23, 2017
Start date January 1, 2017
Est. completion date March 1, 2017

Study information

Verified date August 2017
Source Baskent University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

this study evaluates the effect of cold application after impacted third molar extractions. Patients have bilateral impacted third molar tooth included in this study. Patients do not applied cold after extraction of third molar on one side and applied cold cold after extraction of third molar on the other side.


Description:

Extraction of impacted teeth causes a trauma which results in an inflammatory response. Some postoperative symptoms may occur such as edema, pain, limitations in mouth opening and dysfunction as a consequence of the wisdom tooth extraction surgery.

Local cold application reduces the magnitude of postoperative symptoms. The physiological effects of cold application are as follows: vasoconstriction of blood vessels, blood flow to the region decreases, edema and inflammation decreases, slowdown in cell metabolism and a decrease in local oxygen demand due to the vasoconstriction effect of the cold. Cold therapy also induces muscle constriction which reduces muscle stress, pain and inflammation.


Recruitment information / eligibility

Status Completed
Enrollment 18
Est. completion date March 1, 2017
Est. primary completion date March 1, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- Bilateral bony mandibular third molar impactions

- Has no systemic disease

Exclusion Criteria:

- Different Pell-Gregory classification of impacted teeth

- Previous or current gastric ulcer

- Allergies or hypersensitivities to any common medications

- pregnant or breastfeeding patients

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Cold application


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Baskent University

Outcome

Type Measure Description Time frame Safety issue
Primary Post operative Visual Analogue Scale Scores pre-operative-postoperative 7th day
Primary Post operative facial swelling pre-operative-postoperative 7th day
Primary Post-operative mouth opening pre-operative-postoperative 7th day
Secondary Complications after impacted third molar removal pre-operative-postoperative 7th day
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