Periimplant Bone Changes in Different Abutment Heights and Insertion Timing in Posterior Mandibular Areas
NCT ID: NCT04340726
Last Updated: 2020-04-09
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
NA
INTERVENTIONAL
2015-01-01
2015-12-31
Brief Summary
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Material and methods: The study was planned as a prospective, randomized, controlled parallel group including subjects in need of two implants for the restoration of an edentulous posterior mandibular area. Data were gathered on age, gender, attached gingiva height, bleeding on probing (BoP), smoking habits and previous periodontitis. The patients were allocated into three groups: Group A implants were immediately connected to 2 mm height abutments; Group B implants were immediately connected to 1 mm height abutments; Group C implants were left to heal in a sub-mucosal position and 2 mm abutments were inserted in a second stage surgery. Peri-apical radiographs were taken at the implant surgery (baseline), 4 weeks after surgery (T1), 16 weeks after implant placement at the final restoration delivery (T2) and 1-year after implant placement (T3).
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
Interventions
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One time abutment
Eligibility Criteria
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Inclusion Criteria
* American Society of Anaesthesiologists (ASA) status I;
* no systemic medication or condition known to potentially alter bone metabolism; - absense of acute periodontal condition.
Exclusion Criteria
* need for bone regeneration procedures during surgery;
* inability to correct place the implant in accordance with the prosthetic requirements.
18 Years
ALL
Yes
Sponsors
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Universidade Católica Portuguesa
OTHER
Responsible Party
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Tiago Borges
Professor
Locations
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Universidade Católica Portuguesa
Viseu, , Portugal
Countries
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Other Identifiers
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02/2015
Identifier Type: -
Identifier Source: org_study_id
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