Status:

COMPLETED

Effectiveness in Limiting the Need to Elevate the Maxillary Sinus

Lead Sponsor:

International Piezosurgery Academy

Conditions:

Alveolar Bone Loss

Eligibility:

All Genders

19+ years

Phase:

NA

Brief Summary

The aim of the present study is to evaluate the effectiveness of different alveolar preservation procedures performed at the time of extraction of the first or second upper molar in avoiding a maxilla...

Detailed Description

Bone resorption and contraction of bone volumes are physiologically occurring after the extraction of any dental element. This reabsorption of the alveolar process results in a reduction in the size o...

Eligibility Criteria

Inclusion

  • indication for extraction of the first or second upper molar, based on a thorough diagnosis and treatment plan;
  • "three-rooted" anatomy of the first or second upper molar to be extracted so that it can have an inter-radicular septum that allows a precise measurement of the height of the bone ridge from the septum itself and from the walls of the 3 alveoli to the floor of the maxillary sinus;
  • Extraction of intercalate molar or last arch element;

Exclusion

  • Anatomy of the molar with unique root or fused roots
  • contextual extraction of the molar and one or more contiguous elements
  • apical lesions with a diameter of\> 3 mm or cystic lesions with respect to the element to be extracted
  • root fracture which has produced resorption or bone fenestration
  • 1\) acute myocardial infarction in the last six months; 2) uncontrolled clotting disorders; 3) uncontrolled diabetes (HBA1c\> 7.5%); 4) radiotherapy in the head / neck district for the last 24 months; 5) immunocompromise (eg HIV infection or chemotherapy over the last 3 years); 6) treatment in progress or with bisphosphonates via e.v .; 7) autoimmune diseases in chronic therapy with methotrexate or other immunosuppressive drugs; 8) allergy to bovine collagen; 9) psychological or psychiatric problems; 10) abuse of alcohol or drug use; 11) uncontrolled periodontal disease;

Key Trial Info

Start Date :

October 31 2017

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 28 2018

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT03357705

Start Date

October 31 2017

End Date

December 28 2018

Last Update

March 20 2019

Active Locations (1)

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Piezosurgery Academy

Parma, Italy, 43100