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
PHASE2
40 participants
INTERVENTIONAL
2010-03-31
2010-12-31
Brief Summary
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Methods: The investigators included 34 pregnant women between 15 and 43 who had at least 4 teeth with probing depth ≥ 4 mm or clinical attachment loss ≥ 3 mm, with bleeding on probing in the same place. Women were divided into two groups, the group 1 received supra and subgingival scaling associated with oral hygiene orientation (OHO) and the group 2 received only supragingival scaling with OHO too.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Supra/subgingival therapy
The experimental group received supra and subgingival scaling associated with oral hygiene orientation (OHO)
Supra/subgingival scaling using periodontal curette scraping
The experimental group received supra and subgingival therapy with periodontal curettes
Supra and subgingival scaling
The experimental group received supra and subgingival scaling.
Control group
Control group received only supragingival scaling with OHO too.
Supra/subgingival scaling using periodontal curette scraping
The experimental group received supra and subgingival therapy with periodontal curettes
Supra and subgingival scaling
The experimental group received supra and subgingival scaling.
Interventions
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Supra/subgingival scaling using periodontal curette scraping
The experimental group received supra and subgingival therapy with periodontal curettes
Supra and subgingival scaling
The experimental group received supra and subgingival scaling.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
15 Years
43 Years
FEMALE
No
Sponsors
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Universidade Federal do Maranhão
OTHER
Responsible Party
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Danielli Maria Zucateli Feitosa
MsC
Other Identifiers
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UFMA-2011-DANI
Identifier Type: -
Identifier Source: org_study_id
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