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Prospective Evaluation of Anorganic Bovine Bone Mineral Versus Calcium Phosphosilicate Alloplastic Bone Putty in Direct Sinus Augmentation: a Spilt-mouth Study

NCT01942304 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2019-11-01

No results posted yet for this study

Summary

The purpose of this split-mouth clinical study is to evaluate the clinical, radiographic and histological outcomes of lateral window sinus augmentation with a bovine xenograft or a CPS putty bone substitute in posterior maxillary sites and the survival of implants placed in these sites following healing.

Conditions

  • Sinus Floor Augmentation
  • Maxillary Sinus

Interventions

PROCEDURE

Calcium phosphosilicate alloplastic bone putty in direct sinus augmentation

PROCEDURE

Anorganic bovine bone mineral in direct sinus augmentation

Sponsors & Collaborators

Principal Investigators

  • Georgios A Kotsakis, DDS · University of Minnesota

  • James E Hinrichs, DDS, MS · University of Minnesota

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-10-01
Primary Completion
2018-02-01
Completion
2019-05-31

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT01942304 on ClinicalTrials.gov