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Sinus Lift With Newly Forming Bone and Inorganic Bovine Bone

NCT03419338 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 16

Last updated 2018-02-01

No results posted yet for this study

Summary

The aim of this study is to evaluate the efficacy of newly forming bone graft (NFB) in the gain of bone volume in sinus lift procedures. For that, it will be compared the tomographic bone gain 6 months after surgery between a group that received inorganic bovine bone alone (n=8) and a group that received inorganic bovine bone associated with NFB (n=8).

Conditions

  • Maxillary Sinus

Interventions

PROCEDURE

Sinus lift

Using a lateral access, the Schneider membrane will be elevated using curettes allowing the insertion of graft material.

PROCEDURE

Surgical alveolus

Using a round diamond bur, a surgical alveolus will be created on an toothless ridge region.

PROCEDURE

Inorganic bovine bone + newly forming bone

Maxillary sinus lift will be done with inorganic bovine bone associated with newly forming bone. The newly forming bone will be collected from surgical alveolus previous prepared.

PROCEDURE

Inorganic bovine bone

Maxillary sinus lift will be done with inorganic bovine bone.

DEVICE

Collagen membrane

At the end of the sinus lift, a collagen membrane will be used to obliterate the graft inside the maxillary sinus.

Sponsors & Collaborators

  • University of Sao Paulo

    lead OTHER

Principal Investigators

  • Adriana CP Sant'Ana, PhD · Bauru School of Dentistry - University of Sao Paulo

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
25 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-03-01
Primary Completion
2013-06-01
Completion
2013-06-30

Countries

  • Brazil

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 NCT03419338 on ClinicalTrials.gov