Comparison Between Rapid and Slow Palatal Expansion: Evaluation of Periodontal Indices
NCT ID: NCT01888666
Last Updated: 2013-08-15
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
20 participants
OBSERVATIONAL
2013-01-31
Brief Summary
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Materials and methods: 10 patients will selected and submitted to RPE treatment; other 10 patients will selected and submitted to SPE treatment. The patients will treated with the Haas appliance. In both the groups the periodontal clinical indices (plaque index, PI; papillary bleeding index, PBI; probing pocket depth, PPD) will collected three times during the treatment (before, during and at the end). All measurements will performed by the same examiner.
A descriptive statistical analysis will conducted. The paired samples Student's T test will used to evaluate the intra-group differences between t1 and t2. The unpaired samples Student's T test will used to evaluate between groups differences at t1 and t2. The significance level will set at 95%.
Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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rapid palatal expansion (RPE) using the Haas appliance
No interventions assigned to this group
slow palatal expansion (SPE)
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* necessity of performing a expansion treatment
Exclusion Criteria
6 Years
10 Years
ALL
No
Sponsors
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University of L'Aquila
OTHER
Responsible Party
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Enrico Marchetti
Contract professor
Locations
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Dept. of Life, Health and Environmental Science, University of L'Aquila
L’Aquila, AQ, Italy
Countries
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Other Identifiers
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Tecc01/2013
Identifier Type: -
Identifier Source: org_study_id