Study Results
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View full resultsBasic Information
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COMPLETED
NA
62 participants
INTERVENTIONAL
2008-08-31
2009-02-28
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Cyanoacrylate
3 applications of cyanoacrylate (48 hours interval)at the cervical region of the sensitive tooth
Cyanoacrylate
3 applications of cyanoacrylate (48 hours interval) at the cervical region of the sensitive tooth
Laser
3 Low intensity laser application (48 hour interval). The application of 1Joule/cm\^2 was performed for eight seconds at three points along the dental neck, using the infrared wavelength (795nm)
Laser
This process was conducted three times with an interval of 48 hours between applications, according to laser's manufacturer advice Clean Line Easy Laser - LILT®, Clean Line Easy Laser Doctor Dental Products Industry LTDA, BRA). For dentin hypersensitivity, the application of 1Joule/cm\^2 is recommended for eight seconds at three points along the dental neck, using the infrared wavelength (795nm).
Interventions
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Cyanoacrylate
3 applications of cyanoacrylate (48 hours interval) at the cervical region of the sensitive tooth
Laser
This process was conducted three times with an interval of 48 hours between applications, according to laser's manufacturer advice Clean Line Easy Laser - LILT®, Clean Line Easy Laser Doctor Dental Products Industry LTDA, BRA). For dentin hypersensitivity, the application of 1Joule/cm\^2 is recommended for eight seconds at three points along the dental neck, using the infrared wavelength (795nm).
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. present complaints of dental sensitivity to cold, sweet, acidic foods and brushing;
3. present complaints of pain in teeth located in different quadrants;
4. manifest pain or discomfort upon application of the triple syringe air jet;
5. not be in current use of desensitizing agents.
Exclusion Criteria
2. undergoing orthodontic treatment;
3. frequent use of analgesics, antidepressants and anti-inflammatory drugs;
4. presence of gingival inflammation;
5. non-consent of patient.
12 Years
60 Years
ALL
Yes
Sponsors
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Federal University of the Valleys of Jequitinhonha and Mucuri
OTHER
Federal University of São Paulo
OTHER
Responsible Party
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Olga Flecha
PHD student
Principal Investigators
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Olga D. Flecha, pHD student
Role: PRINCIPAL_INVESTIGATOR
UNIFESP - Federal University of São Paulo, Brazil
Other Identifiers
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odf2008
Identifier Type: -
Identifier Source: org_study_id
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