Status:

COMPLETED

Efficacy of Sinus Floor Augmentation Using Large or Small Bovine Bone Mineral.

Lead Sponsor:

Hadassah Medical Organization

Conditions:

Sinus Graft

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The aim of this clinical study is to compare the amount of newly formed bone after bone augmentation with Bio-Oss® (BO) 0.25-1 mm vs. Bio-Oss® (BO) 1-2 mm in the sinus floor augmentation procedure bil...

Detailed Description

the use of bovine bone mineral particles (Bio-Oss®)in sinus floor augmentation is well established. bovine bone mineral is an oseoconductive material which serves as a space maintainer and a scaffold ...

Eligibility Criteria

Inclusion

  • The patients included in this study are over 18 year old men and women.
  • The patient must be a candidate for sinus floor augmentation.
  • The patient is able to comply with the study-related procedures such as exercising good oral hygiene and attending all follow-up procedures.
  • The patient is able to fully understand the nature of the proposed surgery and is able to provide a signed informed consent.

Exclusion

  • Pregnant women.
  • People who smoke more than 10 cigarettes a day.
  • Alcohol and drug abusers.
  • People suffering from uncontrolled diabetes, severe osteoporosis, rheumatic arthritis, precancer or neoplastic lesions of oral cavity.
  • The patient is nursing.

Key Trial Info

Start Date :

March 1 2007

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

December 1 2008

Estimated Enrollment :

10 Patients enrolled

Trial Details

Trial ID

NCT00426322

Start Date

March 1 2007

End Date

December 1 2008

Last Update

September 10 2013

Active Locations (1)

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Hadassah Medical Organization

Jerusalem, Israel