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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04437316
Other study ID # 2019-00949
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date July 1, 2020
Est. completion date December 31, 2021

Study information

Verified date November 2020
Source University of Zurich
Contact Mona Schiefersteiner, Dr.
Phone 0041 44 634 32 90
Email mona.schiefersteiner@zzm.uzh.ch
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim is to test the effect of low level laser therapy on the relief of symptoms after wisdom tooth removal.


Description:

Each Patient will get all four wisdom teeth removed, left and right side separately. After the operation, low level laser therapy is applied intra- and extraorally. Two different lasers are used, one for each side. The two lasers look identical. Only one of the lasers has therapeutic light, the other one shows just non-therapeutic red light. The effect of the low level laser is measured by several parameters and they are compared with the other side. These parameters are pain, swelling and mouth opening. The selection of the lasers to the sides is double-blind and randomized.


Recruitment information / eligibility

Status Recruiting
Enrollment 20
Est. completion date December 31, 2021
Est. primary completion date June 30, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Indication for prophylactical wisdom tooth removal - 4 wisdom teeth Exclusion Criteria: - pregnancy - taking blood thinners - known infectious diseases - untreated diabetes mellitus - taking immunosuppressants - Previous infections in the area of the wisdom teeth - smoking

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Use of Low level Laser after wisdom tooth removal
Directly after the wisdom teeth removal of the right/left side, one of the low level laser (therapeutic and non-therapeutic (Placebo)) is used.

Locations

Country Name City State
Switzerland Center of dental medicine Zürich

Sponsors (1)

Lead Sponsor Collaborator
University of Zurich

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Postoperative Pain Measurement of Pain with a visual analogue scale (VAS) 0-10 3 days after wisdom tooth removal
Secondary Postoperative Pain Measurement of Pain with a visual analogue scale (VAS) 0-10 7 days after wisdom tooth removal
Secondary Postoperative Swelling Measurement of swelling with an extraoral scan 3 and 7 days after wisdom tooth removal
Secondary Postoperative Mouth opening Measurement of mouth opening 3 and 7 days after wisdom tooth removal
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