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Bone Quality and Quantity Following Guided Bone Regeneration

This study is not yet open for participant recruitment.
Verified April 2011 by Hadassah Medical Organization
Sponsor:
Information provided by:
Hadassah Medical Organization
ClinicalTrials.gov Identifier:
NCT01361321
First received: May 18, 2011
Last updated: March 18, 2012
Last verified: April 2011
History of Changes

May 18, 2011
March 18, 2012
June 2011
June 2014   (final data collection date for primary outcome measure)
Volume of the new bone formed after a GBR procedure [ Time Frame: Volume of the new bone formed after the GBR procedure will be determined 6-7 months after the GBR procedure and before the insertion of dental implants. ] [ Designated as safety issue: No ]
Bone volume obtained following a GBR procedure will be detemined through a comparison of a 3 dimensional analysis of computed tomography images done before and after the GBR procedure.
Same as current
Complete list of historical versions of study NCT01361321 on ClinicalTrials.gov Archive Site
Bone quality [ Time Frame: Bone quality will be assesed through histological analysis that will be carried out at the time of implants insertion 7-8 months after the GBR procedure. ] [ Designated as safety issue: No ]
The collected bone sample will be subjected to histo-morphometric analysis in order to determine the size, shape and orientation of the bony trabeculae,the size and porosity of the bony cortex in addition to the new bone/ bone substitute ratio.
Same as current
Not Provided
Not Provided
 
Bone Quality and Quantity Following Guided Bone Regeneration
Examining Bone Quantity and Quality Following Standard Guided Bone Regeneration Procedures

Edentulism refers to a state of full or partial lack of teeth. This situation may interfere with essential functions such as mastication, speech and even appearance.

Dental implants inserted to the mandible or maxilla is a common treatment modality aiming to restore edentulus alveolar ridges by providing support and anchorage for removable or fixed dental prosthesis.There are cases which in addition to a lack of teeth suffer from lack of sufficient bone tissue volume to support the dental implant.A situation like this may originate from a variety of reasons such as residual bone atrophy, prior alveolar bone destruction due to periodontal disease and even a traumatic tooth extraction. In such cases, a routine alveolar bone augmentation is done to enable a dental implant installation at this site.Guided bone regeneration (GBR) is a widely used technique used to augment edentulus bone ridges. It relies on an inert membrane covering a bone substitute placed over the bony site requiring augmentation. The bone substitute provides a scaffold to alveolar regeneration by the host's osteoblasts while the membrane prevents unwanted epithelial cells to migrate to the bony defect area.

The investigators research is a aimed to preform a follow up after patients who already went through a GBR procedure and before inserting a dental implant. Patients answering the inclusion but not the exclusion criteria will go through an alveolar computerized tomography (C.T) done routinely before inserting dental implants.At the day of Dental implantation - residual bone left from the site of implantation (after preparing the site with a trephine bur) will be taken to a histological analysis. The results from the C.T and the histological examination will be analyzed for bone quantity (volume) and quality and will allow a comparison of bone characteristics obtained by using different routinely used bone substitutes.
Not Provided
Observational
Observational Model: Cohort
Time Perspective: Cross-Sectional
Not Provided
Retention:   Samples Without DNA
Description:

Reisdual bone tissue formed while preparing alveolar bone for dental implant (by drilling with a trephine bur)
Non-Probability Sample

Healty over 18 years of age Patients who went through a GBR procedure previous to an insertion of a dental implant which hasn't been insertd yet
Alveolar Ridge Augmentation
Not Provided
patients after GBR procedure
The study will comprise of patients who already underwent a routine Guided Bone Regeneration (GBR) procedure in order to augment a bony ridge before dental implant insertion. The patients will be followed up in order to determine bone quality and quantity formed after the usage of routinely used bone substitutes during GBR procedure.
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Not yet recruiting
50
October 2014
June 2014   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Healthy men and women over 18 years of age, eligible for signing
  2. Patients who went through a GBR procedure previous to an insertion of a dental implant which hasn't been inserted yet
  3. Patients who understand the meaning of the treatment (routine dental implant insertion) and the follow up study, and approves participation in booth of them

Exclusion Criteria:

  1. Pregnant or nursing women. children or non judgemental patients
  2. Patients with uncontrolled diabetas mellitus, rheumatoid arthritis or osteoporosis.
  3. Patients with a pathology present near the site of dental implantation
Both
18 Years and older
Yes
Contact: Lior Shapira, Professor +972-2-6776126 shapiral@cc.huji.ac.il
Israel
 
NCT01361321
bondbone-HMO-CTIL
No
Arik Tzukert, DMD, Hadassah Medical Organization
Hadassah Medical Organization
Not Provided
Principal Investigator: Lior Shapira, Professor Department of Periodontology
Hadassah Medical Organization
April 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP