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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: |
NCT02603198 |
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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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2%-Mepivacaine With Two Different Vasoconstrictors Solutions in Third Molar Surgery a Comparative Study
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Scientific title:
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2%-Mepivacaine With Two Different Vasoconstrictors; 1:20.000 Levonordefrin or 1:100.000 Epinephrin for Local Anesthesia in Third Molar Surgery: A Comparative Randomized Clinical Trial |
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Date of first enrolment:
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August 2014 |
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Target sample size:
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30 |
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Recruitment status: |
Active, not recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT02603198 |
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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: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), 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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Marcelo Minharro Cechetti, 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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Post - Doctorate |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- minimum body weight of 50Kg, necessity of bilateral impacted third molar removal
Exclusion Criteria:
Age minimum:
18 Years
Age maximum:
40 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Pain
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Edema
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Trismus
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Intervention(s)
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Drug: mepivacaine chloridrato epinephrine
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Drug: mepivacaine chloridrato levonordefrin
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Primary Outcome(s)
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Change in Blood pressure values
[Time Frame: 20 minutes pre-operatory, 5 minutes before surgery, 5 minutes after anesthesia, 10 minutes after suture]
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Secondary Outcome(s)
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Change in Heart Rate values
[Time Frame: 20 minutes pre-operatory, 5 minutes before surgery, 5 minutes after anesthesia, 10 minutes after suture]
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Pain
[Time Frame: 6, 8,24 and 48 hours after suture]
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Bleeding
[Time Frame: after 1 hour postoperatively]
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Secondary ID(s)
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34147114500000068
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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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