- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05657223
Factors Associated With the Complexity of Dental Implant Surgery After Alveolar Ridge Preservation: A Retrospective Cross-sectional Study
December 19, 2022 updated by: Kaohsiung Medical University Chung-Ho Memorial Hospital
Attending Physician, Division of Periodontics, Department of Dentistry, Kaohsiung Medical University Hospital, Kaohsiung
Alcohol consumption, tooth position, and periodontitis-related tooth extraction affect the complexity of subsequent implant surgery after alveolar ridge preservation.
Study Overview
Status
Completed
Conditions
Detailed Description
Materials and methods We retrospectively analyzed the dentition of 165 alveolar ridge preservation sites in 116 patients.
The bone width at three different vertical levels was measured on cone beam computed tomography images, and a comparison of bone regeneration requirements for subsequent dental implant surgery was performed for different socket types.
Study Type
Observational
Enrollment (Actual)
165
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
16 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Of 165 sites, dental implant surgery was performed at 156 sites.
A total of 72 damaged sockets and 93 intact sockets were included.
Description
Inclusion Criteria:
- teeth extraction in the premolar and molar regions, who underwent flapless tooth extraction with alveolat ridge preservation (ARP) and filling with freeze-dried bone allograft (FDBA) and platelet-rich fibrin (PRF), who underwent cone beam computed tomography (CBCT) followed by dental implant surgery after tooth extraction, and with adequate oral hygiene
Exclusion Criteria:
- untreated periodontitis, systemic disease, or the of medication that influences bone metabolism
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Crossover
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Alveolar bone width
Time Frame: 4~6 months
|
4~6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2015
Primary Completion (Actual)
December 31, 2019
Study Completion (Actual)
December 31, 2019
Study Registration Dates
First Submitted
December 12, 2022
First Submitted That Met QC Criteria
December 19, 2022
First Posted (Estimate)
December 20, 2022
Study Record Updates
Last Update Posted (Estimate)
December 20, 2022
Last Update Submitted That Met QC Criteria
December 19, 2022
Last Verified
December 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- KMUHIRB-E(I)-20210023
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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