Trial to Evaluate the Efficacy on Local Anesthesia and Safety of 2% Lidocaine HCl With Different Epinephrine Concentration in Patients Undergoing Surgical Extraction of Impacted Lower Third Molars
NCT ID: NCT02696369
Last Updated: 2016-03-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
65 participants
INTERVENTIONAL
2014-12-31
2015-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
QUADRUPLE
Study Groups
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2% Lidocaine HCL:Epinephrine inj.
2% Lidocaine HCL with epinephrine 1:200,000
2% lidocaine HCl with epinephrine 1:200,000
2% Lidocaine HCL:Epinephrine inj. (3M)
2% Lidocaine HCl with epinephrine 1:80,000
2% lidocaine HCl with epinephrine 1:80,000
Interventions
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2% lidocaine HCl with epinephrine 1:200,000
2% lidocaine HCl with epinephrine 1:80,000
Eligibility Criteria
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Inclusion Criteria
* Physical grade 1 or 2 by American Society of Anesthesiologists (ASA)
* Mesioangular or horizontal angulation categorized by winter classification
Exclusion Criteria
* Any infection or edema during the extraction
* The following patients: clotting disorder, hyperthyroidism, arteriosclerosis, cardiac insufficiency, other cardiovascular disorders
* Pregnancy or breast-feeding
* Any conditions that the investigator considers not to appropriate for this study
19 Years
ALL
No
Sponsors
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Huons Co., Ltd.
INDUSTRY
Responsible Party
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Locations
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Huons
Ansan, Kyeonggi-do, South Korea
Countries
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Other Identifiers
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HU-015
Identifier Type: -
Identifier Source: org_study_id
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