Early and Late Implant Failure
Implant Failure and Risk Indicators
1 other identifier
observational
190
1 country
1
Brief Summary
The aim of this study was to evaluate the early and late implant loss rate in a sample of patients who had received implant-supportive restorative therapy in a university setting. Moreover, the study aimed to identify patient- and implant-related variables for implant failure
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 Oct 2017
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
October 5, 2017
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 14, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
April 24, 2019
CompletedFirst Submitted
Initial submission to the registry
February 12, 2020
CompletedFirst Posted
Study publicly available on registry
February 17, 2020
CompletedFebruary 17, 2020
February 1, 2020
1.4 years
February 12, 2020
February 12, 2020
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Implant survival
Early implant loss and late implant loss
October 2017 to March 2019
Secondary Outcomes (1)
Implant failure
October 2017 to March 2019
Interventions
We procedure to observed clinically the sample size, to be able to determine if the dental implant was present or no. If the implant was absent we recorded if it was early( prior to restoration) or late ( after prosthesis was delivered).
Eligibility Criteria
A sample of men and women over 18 years old, which they had received an implant-supportive restorative therapy in a university setting throughout a period of at least 7 years.
You may qualify if:
- Men and women over 18 years old
- Partially or totally edentulous patients with at least one implant placed at the university and at least 7 years before.
- Cemented, screwed, or mechanically retained prosthesis.
- Single and partial prostheses, as well as complete arch prosthesis (fixed and removable).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Joan
Barcelona, 08025, Spain
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Joan Takamoli
Universitat Internacional de Catalunya
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Target Duration
- 1 Day
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- DDS
Study Record Dates
First Submitted
February 12, 2020
First Posted
February 17, 2020
Study Start
October 5, 2017
Primary Completion
March 14, 2019
Study Completion
April 24, 2019
Last Updated
February 17, 2020
Record last verified: 2020-02