Survival and Success Rates of 6mm Implants With a Micro-rough Surface After 4.5 - 18.2 Years in Function
1 other identifier
observational
74
1 country
1
Brief Summary
In this retrospective study, approximately 60 patients treated with 6mm short implants (Straumann, SLA (sandblasted, large-grit, acid-etched surface), SLActive (sandblasted, large-grit, acid-etched, hydrophilic surface), 4.1 or 4.8 mm in diameter) will be followed for 4.5-18.2 years. Clinical and radiographic parameters will be assessed in a follow-up examination.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started May 2018
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
May 9, 2018
CompletedFirst Submitted
Initial submission to the registry
April 3, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 8, 2019
CompletedFirst Posted
Study publicly available on registry
July 12, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
June 30, 2020
CompletedSeptember 3, 2020
September 1, 2020
11 months
April 3, 2019
September 2, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Implant survival rates
Survival rates of short dental implants
5-18 years
Secondary Outcomes (10)
Radiographic: Annual bone loss
5-18 years
Clinically: modifying risk factors on implant survival and success
5-18 years
Clinically: modifying risk factors on implant survival and success
5-18 years
Clinically: modifying risk factors on implant survival and success
5-18 years
Clinically: modifying risk factors on implant survival and success
5-18 years
- +5 more secondary outcomes
Study Arms (1)
6 mm implants
Patients were treated with 6mm short implants (Straumann, SLA, SLActive, 4.1 or 4.8 mm in diameter).
Interventions
Eligibility Criteria
All patients treated with a 6mm short implant at the University of Bern were recalled for a clinical and radiographic follow-up examination.
You may qualify if:
- Partially or fully edentulous jaw
- Written informed consent
You may not qualify if:
- Pregnant women/lactating women
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Department for oral surgery of the zmk Bern, University of Bern
Bern, 3010, Switzerland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Vivianne Chappuis, DMD
University of Bern
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 3, 2019
First Posted
July 12, 2019
Study Start
May 9, 2018
Primary Completion
April 8, 2019
Study Completion
June 30, 2020
Last Updated
September 3, 2020
Record last verified: 2020-09