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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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23 May 2016 |
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Main ID: |
NCT02602431 |
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Date of registration:
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08/11/2015 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Low Laser Light Therapy After Impacted Third Molar Removal
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Scientific title:
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A Unique Application of Low Laser Therapy After Third Molar Surgery: A Randomized Controlled Clinical Trial |
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Date of first enrolment:
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March 2014 |
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Target sample size:
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30 |
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Recruitment status: |
Recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT02602431 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Treatment
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Phase:
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N/A
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Countries of recruitment
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Brazil
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Contacts
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Name:
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Maria Cristina Deboni, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Associate Professor |
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Name:
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Maria Cristina Deboni, PhD |
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Address:
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Telephone:
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+5511984269925 |
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Email:
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mczdebon@usp.br |
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Affiliation:
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Name:
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Maria Cristina Deboni, PhD |
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Address:
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Telephone:
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11.55 28488185 |
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Email:
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mczdebon@usp.br |
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Affiliation:
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- necessity of bilateral impacted third molar removal with similar dental arch
positioning and similar surgical difficulty.
Exclusion Criteria:
- Compromised Systemic Health status, Neurologic and/or mental disorders, local
infection history, anti-inflammatory or analgesic use for the last 15 days, tabagism,
ethylism, pregnancy.
Age minimum:
18 Years
Age maximum:
35 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Edema
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Pain
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Trismus
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Intervention(s)
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Device: Intra-oral laser irradiation
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Device: Intra-oral Placebo
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Device: Extra-oral placebo
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Device: Extra-oral laser irradiation
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Primary Outcome(s)
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Change in Pain Scores on the Visual Analog scale
[Time Frame: 4, 6, 8, 24, 48hours post operative period]
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Secondary Outcome(s)
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mouth aperture in millimeters
[Time Frame: 24 hours after surgery]
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Edema percentage
[Time Frame: 24 hours after surgery]
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Secondary ID(s)
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31861414.4.0000.0075
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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