CompletedNot Applicable

Influence of Thickness of the Peri-implant Soft Tissue on Marginal Bone Remodeling

Italy100 participantsStarted 2017-01-15

Plain-language summary

The aim of this observational study is the evaluation of marginal bone remodeling after surgical implant placement, correlating the gingival thickness with the bone resorption rate.

Who can participate

Age range18 Years

SexALL

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Inclusion criteria

✓. indications for intervention of implant placement in posterior mandible (premolar / molar region) based on a careful diagnosis and treatment plan;
✓. presence of a residual osseous crest with a minimum of 7 mm surgical height, and thickness of at least 6 mm at the level of the programmed implant site;
✓. the bone crest must be healed (at least 6 months after the loss / extraction of the element corresponding tooth);
✓. absence of regenerated bone;
✓. plaque index of less than 25% and bleeding index lower than 20%;
✓. bucco-lingual width of the attached gingiva ≥ 4 mm;
✓. insertion torque plant inserito≥35 N / cm;
✓. patient age\> 18 years;

Exclusion criteria

✕. acute myocardial infarction in the last two months;
✕. blood coagulation disorders not compensated;
✕. uncontrolled diabetes (HbA1c\> 7.5%);
✕. radiation therapy of the district head / neck in the last 24 months;
✕. immunocompromised patients (HIV infection or chemotherapy) within the last 5 years);
✕. present or past treatment with intravenous bisphosphonates;
✕. psychological or psychiatric diseases;
✕. alcohol or drug abuse;

What they're measuring

peri-implant bone resorption

Timeframe: from baseline to twelve months

Trial details

NCT IDNCT03077880

SponsorInternational Piezosurgery Academy

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2018-07-15

View on ClinicalTrials.gov More Alveolar Bone Loss trials