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Comparison Synthetic Hydroxyapatite and Inorganic Bovine Bone in Sinus Floor Elevation

NCT03077867 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 88

Last updated 2021-03-26

No results posted yet for this study

Summary

This is set as prospective clinical trial to correlate histologically and radiologically the performance of four different bone grafts (synthetic hydroxyapatite alone, synthetic hydroxyapatite mixed with polylactic-polyglycolic acid, synthetic hydroxyapatite with i-PRF and inorganic bone graft) in the sinus floor elevation technique with lateral approach for the treatment of atrophic crests.

Conditions

  • Alveolar Bone Loss

Interventions

PROCEDURE

sinus floor augmentation with bone graft

sinus floor augmentation with lateral approach with bone graft

Sponsors & Collaborators

  • University of Trieste

    collaborator OTHER

  • International Piezosurgery Academy

    lead OTHER

Principal Investigators

  • Claudio Stacchi, Dr. · Piezosurgery Academy

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-01-15
Primary Completion
2020-03-15
Completion
2021-03-15

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03077867 on ClinicalTrials.gov