Impact of Buccal Bone Thickness on Pathological Peri-implant Bone Loss: A 3-year Prospective Cohort Study
NCT ID: NCT02939222
Last Updated: 2020-04-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
WITHDRAWN
NA
INTERVENTIONAL
2016-10-01
2023-12-01
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Marginal Bone Loss in Dental Implants
NCT03232372
Bone Dimensional Changes at Different Implant-to-abutment Connections: a 1-year Clinical and Radiological Study
NCT01807416
Dimensional Changes of Peri-implant Facial Bone
NCT01821092
Peri-implant Bone Changes in Post-menopausal Osteoporotic Women
NCT02884401
Influence of the Implant Connection on Facial Tissues Maturation
NCT04160689
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Routine implant placement
No comparison needed
Implant placement
Routine implant placement in the ideal three dimensional implant position
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Implant placement
Routine implant placement in the ideal three dimensional implant position
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Patients requiring oral rehabilitation through supported prosthesis
* Patients with partial edentulism
* No antibiotic in the last 2 months
* No smoking or smoking \<10 cigarettes a day
Exclusion Criteria
* Implants that because prosthetic characteristics can not be registered probing depth or attachment level appropriately
* Smoking\> 10 cigarettes a day
* Pregnant Patients
* Implants that can not be followed in CICOM
* Patients who do not return to regular maintenance therapy every 3-6meses
* Patients who are not controlled periodontal disease
18 Years
80 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Center of Implantology, Oral and Maxillofacial Surgery, Badajoz, Spain
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Centro de Implantologia Cirugia Oral y Maxiofacial
Badajoz, , Spain
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
18002909-2
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.