- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03145246
Long-Term Outcome Following Regenerative Periodontal Treatment of Intrabony Defects
May 5, 2017 updated by: Mahidol University
Long-Term Outcome Following Regenerative Periodontal Treatment of Intrabony Defects: A Retrospective Study at Mahidol University
Many years ago, periodontal regenerative treatment has been done in Periodontics and Oral Medicine Clinic, Faculty of Dentistry, Mahidol University, Bangkok, Thailand.
However, there is still lacking of study about long-term result of periodontal regenerative treatment of intrabony defects.
Study Overview
Status
Completed
Conditions
Detailed Description
Beside, in the present, some materials for periodontal regenerative treatment are still expensive.
Periodontists and patients have to plan together based on not only rationale of treatment but also cost and effectiveness.
Thus the long-term result of treatment could be useful for the decision making.
Study Type
Observational
Enrollment (Actual)
89
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
The patients who received regenerative periodontal therapy of the intrabony defects by post-graduate students at the Periodontics and Oral Medicine Clinic, Faculty of Dentistry, Mahidol University, Thailand and were placed in the Recall Patient Bank from 2000 to 2014.
Description
Inclusion Criteria:
- Patients who received regenerative therapy of the intrabony defects
- Patients who had the record of re-evaluation at 1 year post-surgery
Exclusion Criteria:
- Patients who received regenerative therapy involving the furcation area
- Patients who received non-periodontal regenerative therapy
- Patients who received endodontic regeneration
- Patients who had an incomplete periodontal data recording
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
tooth loss
regeneration treated teeth loss
|
number of regeneration treated teeth loss
|
|
clinical attachment loss ≥ 2 mm
regenerated treated teeth with clinical attachment loss ≥ 2 mm
|
regenerated treated teeth with clinical attachment loss ≥ 2 mm
|
|
clinical attachment loss loss < 2 mm
regenerated treated teeth with clinical attachment loss < 2 mm
|
regenerated treated teeth with clinical attachment loss ≥ 2 mm
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Percentage of regenerative-treated tooth loss after periodontal regeneration
Time Frame: 1 year
|
Percentage of regenerative-treated tooth loss since 1 year after periodontal regeneration until last visit of supportive periodontal treatment
|
1 year
|
|
Percentage of regenerative-treated sites with clinical attachment loss ≥ 2 mm
Time Frame: 1 year
|
Percentage of regenerative-treated sites with clinical attachment loss ≥ 2 mm since 1 year after periodontal regeneration until last visit of supportive periodontal treatment
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Variables (patient and tooth characteristics) that associated with tooth loss or clinical attachment loss
Time Frame: 1 year
|
Patient variables and tooth characteristics associated with regenerative-treated tooth loss or sites with clinical attachment loss ≥ 2 mm from any supportive periodontal treatment visits (the last supportive periodontal treatment visit) compared to baseline or 1-year after surgery.
|
1 year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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
January 1, 2015
Primary Completion (Actual)
April 1, 2015
Study Completion (Actual)
April 1, 2015
Study Registration Dates
First Submitted
November 13, 2015
First Submitted That Met QC Criteria
May 5, 2017
First Posted (Actual)
May 9, 2017
Study Record Updates
Last Update Posted (Actual)
May 9, 2017
Last Update Submitted That Met QC Criteria
May 5, 2017
Last Verified
May 1, 2017
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2014/DT105
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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