MedTrace Logo

Effectiveness in Limiting the Need to Elevate the Maxillary Sinus

NCT03357705 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2019-03-20

No results posted yet for this study

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 maxillary sinus elevation or at least limiting the size, to allow the insertion of dental implants. The residual bone height will be radiographically evaluated on the sinus sinus floor at the time of extraction and after 6 months by comparing the cases where alveolar preservation is performed using a nanocrystalline synthetic hydroxyapatite graft (group A) with cases where the procedure of alveolar preservation is performed using bovine collagen sponge (group B).

Conditions

  • Alveolar Bone Loss

Interventions

PROCEDURE

alveolar ridge preservation with synthetic bone

after tooth extraction

PROCEDURE

alveolar ridge preservation with bovine collagen

after tooth extraction

Sponsors & Collaborators

  • International Piezosurgery Academy

    lead OTHER

Principal Investigators

  • Claudio Stacchi, Dr · Piezosurgery Academy

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-10-31
Primary Completion
2018-10-31
Completion
2018-12-28

Countries

  • Italy

Study Locations

More Related Trials

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 NCT03357705 on ClinicalTrials.gov