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.
COMPLETED
190 participants
OBSERVATIONAL
2017-10-05
2019-04-24
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.
Patient's Perception of Complications in Implantology.
NCT04870658
Alveolar Ridge Sequelae Due to Peri-implantitis: a Retrospective Observational Study
NCT04534361
Prediction of Failure of Dental Implants
NCT04129957
Peri-implant Marginal Bone Loss and Implant Failure in Patients With Smoking Habit
NCT05390242
Compliance and Cumulative Interceptive Rate After Therapy of Peri-implantitis
NCT05772078
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.
COHORT
PROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Presence or absence of implant
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
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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).
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Universitat Internacional de Catalunya
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Joan Takamoli
DDS
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Joan Takamoli
Role: PRINCIPAL_INVESTIGATOR
Universitat Internacional de Catalunya
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Joan
Barcelona, , 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.
PER-ECL-2017-04
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.