Short vs Long Dental Implants for the Fixed Rehabilitation of the Fully Edentulous Mandible
Primary Purpose
Edentulous Jaw
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
ASTRA TECH Implant System, OsseoSpeed™ 4.0 S, length: 6 mm
ASTRA TECH Implant System, OsseoSpeed™ 4.0 S, length: ≥11mm
Sponsored by
About this trial
This is an interventional treatment trial for Edentulous Jaw focused on measuring short dental implants, full-arch prosthesis
Eligibility Criteria
Inclusion Criteria:
- total edentulous patients in the lower region since at least 8 months,
- sufficient amount of native bone (no augmentation procedures) in the recipient sites to allow ≥11 mm long and 4 mm wide implant installation (≥1 mm of peri-implant bone circumferentially)
- systemic health
- compliance with good oral hygiene
- informed consent signed.
Exclusion Criteria:
- any disease, medication or drug that could jeopardize healing, osseointegration or treatment outcome,
- untreated caries or periodontitis of the remaining teeth,
- mucosal and bone tissue lesions,
- severe bruxism or other parafunction habits,
- unrealistic aesthetic demands,
- patient taking part to another study
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Short implants
Long implants
Arm Description
A full-arch screw-retained mandibular prosthesis with distal cantilevers supported by five interforaminal short implants (ASTRA TECH Implant System, OsseoSpeed™ 4.0 S, length: 6mm)
A full-arch srew-retained mandibular prosthesis with distal cantilevers supported by five interforaminal short implants (ASTRA TECH Implant System, OsseoSpeed™ 4.0 S, length: ≥11mm)
Outcomes
Primary Outcome Measures
Marginal bone level (MBL) change
Marginal bone level (MBL) is measured as the distance in millimiters calculated on periapical radiographs from the implant neck to the most coronal bone-to-implant contact point at both the mesial and the distal side of each implant. The radiographs will be taken with an X-ray apparatus supplied with a long cone and Rinn's film holders.
Secondary Outcome Measures
Implant survival rate
A surviving implant is defined as an implant in place at the time of the follow-up. Any implant loss shall be assessed as an early loss (implant fails before being osseointegrated) or late loss (after being osseointegrated).
Full Information
NCT ID
NCT03509402
First Posted
March 31, 2018
Last Updated
October 21, 2020
Sponsor
University of Campania "Luigi Vanvitelli"
Collaborators
Dentsply Sirona Implants and Consumables
1. Study Identification
Unique Protocol Identification Number
NCT03509402
Brief Title
Short vs Long Dental Implants for the Fixed Rehabilitation of the Fully Edentulous Mandible
Official Title
Short vs Long Implants Supporting a Total Fixed Prosthetic Rehabilitation of the Fully Edentulous Mandible. A Multicenter Randomized Controlled Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2020
Overall Recruitment Status
Unknown status
Study Start Date
January 2010 (Actual)
Primary Completion Date
February 2021 (Anticipated)
Study Completion Date
February 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Campania "Luigi Vanvitelli"
Collaborators
Dentsply Sirona Implants and Consumables
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The aim of this study is to clinically and radiographically compare the performance of short (6 mm-long) versus long (≥11 mm-long) dental implants placed in the interforaminal region of fully edentulous mandibles, supporting a screw-retained full-arch cantilever bridge.
Detailed Description
The use of short dental implants provides undeniable benefits in sites where the reduced available volume would otherwise need bone augmentation procedures and their use has greatly expanded in the recent years. However, well designed clinical trials which provide a sound evidence of their performance and reliability are still lacking to date.
In this post-market, multi-center, open, parallel-group, randomized, controlled clinical trial the investigators aim to to clinically and radiographically compare the performance of short (6 mm-long) versus long (≥11 mm-long) dental implants supporting a mandibular screw-retained full-arch cantilever bridge.
Five 4mm-wide/6mm-long (test) or 4mm-wide/≥11mm-long (control) titanium dental implants (Osseospeed™, ASTRA TECH Implant System™, Dentsply Sirona) are placed in the interforaminal region of fully edentulous mandibles, in non-regenerated sites, with at least 1 mm of peri-implant bone circumferentially.
All products are CE (European Conformity) marked and used within their intended use.
Two-Stage surgery is performed, implants are positioned in healed bone and exposed after 3 months to be connected with the prosthesis.
This is a medium-term follow-up study including evaluations also at 1 and 3 years from the baseline.
Three italian centers participate: Naples (University of Campania "Luigi Vanvitelli"), Naples (AORN "A. Cardarelli"), Catania (Private Office).
The study protocol has been approved by the Institutional Review Board of the University of Campania "Luigi Vanvitelli".
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Edentulous Jaw
Keywords
short dental implants, full-arch prosthesis
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Short implants
Arm Type
Experimental
Arm Description
A full-arch screw-retained mandibular prosthesis with distal cantilevers supported by five interforaminal short implants (ASTRA TECH Implant System, OsseoSpeed™ 4.0 S, length: 6mm)
Arm Title
Long implants
Arm Type
Active Comparator
Arm Description
A full-arch srew-retained mandibular prosthesis with distal cantilevers supported by five interforaminal short implants (ASTRA TECH Implant System, OsseoSpeed™ 4.0 S, length: ≥11mm)
Intervention Type
Device
Intervention Name(s)
ASTRA TECH Implant System, OsseoSpeed™ 4.0 S, length: 6 mm
Intervention Description
Rehabilitation of the edentulous mandible by a full-arch srew-retained prosthesis with distal cantilevers supported by five interforaminal short implants (ASTRA TECH Implant System, OsseoSpeed™ 4.0 S, length: 6 mm)
Intervention Type
Device
Intervention Name(s)
ASTRA TECH Implant System, OsseoSpeed™ 4.0 S, length: ≥11mm
Intervention Description
Rehabilitation of the edentulous mandible by a full-arch srew-retained prosthesis with distal cantilevers supported by five interforaminal long implants (ASTRA TECH Implant System, OsseoSpeed™ 4.0 S, length: ≥11mm)
Primary Outcome Measure Information:
Title
Marginal bone level (MBL) change
Description
Marginal bone level (MBL) is measured as the distance in millimiters calculated on periapical radiographs from the implant neck to the most coronal bone-to-implant contact point at both the mesial and the distal side of each implant. The radiographs will be taken with an X-ray apparatus supplied with a long cone and Rinn's film holders.
Time Frame
1, 3 and 5 years from baseline (prosthetic loading)
Secondary Outcome Measure Information:
Title
Implant survival rate
Description
A surviving implant is defined as an implant in place at the time of the follow-up. Any implant loss shall be assessed as an early loss (implant fails before being osseointegrated) or late loss (after being osseointegrated).
Time Frame
1, 3 and 5 years from baseline (prosthetic loading)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
total edentulous patients in the lower region since at least 8 months,
sufficient amount of native bone (no augmentation procedures) in the recipient sites to allow ≥11 mm long and 4 mm wide implant installation (≥1 mm of peri-implant bone circumferentially)
systemic health
compliance with good oral hygiene
informed consent signed.
Exclusion Criteria:
any disease, medication or drug that could jeopardize healing, osseointegration or treatment outcome,
untreated caries or periodontitis of the remaining teeth,
mucosal and bone tissue lesions,
severe bruxism or other parafunction habits,
unrealistic aesthetic demands,
patient taking part to another study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Luigi Guida, Prof
Organizational Affiliation
University of Campania "Luigi Vanvitelli"
Official's Role
Principal Investigator
12. IPD Sharing Statement
Citations:
PubMed Identifier
3527955
Citation
Albrektsson T, Zarb G, Worthington P, Eriksson AR. The long-term efficacy of currently used dental implants: a review and proposed criteria of success. Int J Oral Maxillofac Implants. 1986 Summer;1(1):11-25. No abstract available.
Results Reference
background
PubMed Identifier
25123762
Citation
Nisand D, Renouard F. Short implant in limited bone volume. Periodontol 2000. 2014 Oct;66(1):72-96. doi: 10.1111/prd.12053.
Results Reference
background
PubMed Identifier
14714838
Citation
Ekelund JA, Lindquist LW, Carlsson GE, Jemt T. Implant treatment in the edentulous mandible: a prospective study on Branemark system implants over more than 20 years. Int J Prosthodont. 2003 Nov-Dec;16(6):602-8.
Results Reference
background
PubMed Identifier
23413956
Citation
Srinivasan M, Vazquez L, Rieder P, Moraguez O, Bernard JP, Belser UC. Survival rates of short (6 mm) micro-rough surface implants: a review of literature and meta-analysis. Clin Oral Implants Res. 2014 May;25(5):539-45. doi: 10.1111/clr.12125. Epub 2013 Feb 18.
Results Reference
background
PubMed Identifier
19681932
Citation
Laurell L, Lundgren D. Marginal bone level changes at dental implants after 5 years in function: a meta-analysis. Clin Implant Dent Relat Res. 2011 Mar;13(1):19-28. doi: 10.1111/j.1708-8208.2009.00182.x.
Results Reference
background
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Short vs Long Dental Implants for the Fixed Rehabilitation of the Fully Edentulous Mandible
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