Comparative Study Between Lyophilized or Frozen Bone Allografts for Sinus-lifting

Sponsor
University of Sao Paulo (Other)
Overall Status
Unknown status
CT.gov ID
NCT02583737
Collaborator
(none)
15
2
30

Study Details

Study Description

Brief Summary

Bone resorption and atrophy in maxillary posterior region is due to severe periodontal disease and is consequent tooth extractions. Sinus pneumatisation can occur after tooth extraction and alveolar bone loss. Consequently, bone-reducing volume at that region is a great challenge to implantodontists. Sinus lifting surgery have been practiced since 80's and many biomaterials have been used to solve filling issues to maintain the sinus floor lifted in a position that can allow dental implants installation. Bone grafts have shown to be the best choice of filling grafts. Despite autologous bone are the gold standard filling biomaterial it is associates with great mortality and morbidity. So, bone allografts from tissue bank had been shown to be an advantageous alternative. Lyophilized or freeze tissue bone are the most common allografts but literature is poor in randomized controlled parallel clinical trials regarding those filling grafts for sinus lifting. The aim of this study is to perform a randomized controlled clinical trial comparing two bone allografts: lyophilized and freeze bone allografts from human bone tissue bank. The investigators want to verify which one can develop greater osteogenesis, if is there any difference between them regarding the architectural trabeculae formation, if there are different patterns of reabsorption and finally if is there any differences between them regarding primary and lately dental implants stability. To answer those questions the investigators propose firstly, to carry out microtomographic and histological analysis from trephine bone samples after six months of sinus lifting and grafting in healthy participants undergoing osseointegrated dental implants. Secondly, the primary and lately implant stability is going to be achieved employing Resonance Frequency Analysis (RFA).

Condition or Disease Intervention/Treatment Phase
  • Procedure: freeze bone allograft
  • Procedure: lyophilized bone allograft
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
15 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Histological and Microtomographic Comparative Study Between Lyophilized or Frozen Bone Allografts for Sinus-lifting: A Randomized Clinical Trial
Study Start Date :
Jun 1, 2014
Anticipated Primary Completion Date :
Dec 1, 2016
Anticipated Study Completion Date :
Dec 1, 2016

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: group lyophilized bone allograft

sinus lifting with tissue bank lyophilized bone filling

Procedure: lyophilized bone allograft
sinus lifting filling procedure employing lyophilized bone allograft from tissue bone bank.

Active Comparator: group freeze bone allograft

sinus lifting with freeze bone bank filling

Procedure: freeze bone allograft
sinus lifting filling procedure employing freeze bone allograft from tissue bone bank.

Outcome Measures

Primary Outcome Measures

  1. volume of bone neoformation in mm3 [six months after grafting]

    computational software for analysis the micro CT scanning of trephine bone samples images

  2. area of bone neoformation in μm2 [six months after grafting]

    IMAGEJ histomorphometric software for analysis of trephine bone samples micrographic images

Secondary Outcome Measures

  1. dental implants stability value [six months after grafting]

    primary implant stability by Resonance Frequency Analysis (RFA) in ISQ

  2. dental implants stability value [six months after dental implant]

    late stability by Resonance Frequency analysis (RFA) in ISQ

Eligibility Criteria

Criteria

Ages Eligible for Study:
30 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • healthy

  • totally or partially edentulous patients, bilaterally, in upper premolar or molar region; presenting maxillary sinus lifting necessity with bilateral alveolar bone height lower than 5mm and indication for at least one osseointegrated dental implant in premolar or molar region.

Exclusion Criteria:
  • recent sinusitis history

  • hypersensibility for sinus allergens, tabagism, ethylism

  • severe periodontal disease, diabetes, hypertension.

  • Cases that occur schneiderian membrane perforation will be excluded from the final sample.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • University of Sao Paulo

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Maria Cristina Zindel Deboni, Associate Professor, University of Sao Paulo
ClinicalTrials.gov Identifier:
NCT02583737
Other Study ID Numbers:
  • CAEE 30738714.0.0000.0075.
First Posted:
Oct 22, 2015
Last Update Posted:
May 11, 2016
Last Verified:
May 1, 2016
Keywords provided by Maria Cristina Zindel Deboni, Associate Professor, University of Sao Paulo
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 11, 2016