Status:
UNKNOWN
Guided Bone Regeneration With Customized Titanium Meshes
Lead Sponsor:
University of Milan
Conditions:
Bone Resorption
Eligibility:
All Genders
19-90 years
Phase:
NA
Brief Summary
The aims of this prospective clinical study are to evaluate: a) the effectiveness of digitally customized titanium meshes in association with autologous bone particles and bovine bone mineral and cove...
Detailed Description
Objectives: * to evaluate the effectiveness of digitally customized titanium meshes for guided bone regeneration with autologous bone chips taken from the mandibular body and/or ramus mixed with bovi...
Eligibility Criteria
Inclusion
- systemically healthy patients;
- a minimum age of 18 years;
- relevant or severe bone atrophy at the edentulous sites incompatible with placement of even short (≤6 mm) or narrow (\<3 mm) implants in an appropriate and prosthetically guided position;
- adequate compliance of patients, both in terms of oral hygiene and respect the follow-up recalls;
- ability to understand the proposed surgical treatment and to understand and sign the informed consent.
Exclusion
- severe kidney and/or liver disease;
- congenital or acquired immunodeficiency;
- ongoing antiblastic chemotherapy at the time of first examination;
- sequelae of radiotherapy in the head and neck area;
- oral mucosa diseases, such as lichen planus;
- full mouth plaque score (FMPS) and full mouth bleeding score (FMBS) \< 20%;
- non-compliant patients;
- tobacco abuse (\>10 cigarettes per day) or alcohol abuse;
- non compensated diabetes;
- active periodontal disease at the time of first examination ;
- bisphosphonate chemotherapy in progress;
- pregnant women.
Key Trial Info
Start Date :
January 10 2018
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 30 2022
Estimated Enrollment :
24 Patients enrolled
Trial Details
Trial ID
NCT04480073
Start Date
January 10 2018
End Date
December 30 2022
Last Update
July 21 2020
Active Locations (1)
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1
ASST Santi Paolo e Carlo
Milan, Italy, 20142