- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06031896
The Severity of Periodontitis at the Buccal and Palatal Site
September 4, 2023 updated by: The Dental Hospital of Zhejiang University School of Medicine
The Comparison of the Severity of Periodontitis at the Buccal and Palatal Site
To record and compare the periodontal conditions of buccal and palatal sites in patients
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
3000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Zhejiang
-
Hangzhou, Zhejiang, China
- The Affiliated Hospital of Stomatology, Zhejiang University School of Medicine
-
-
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
- Adult
- Older Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Probability Sample
Study Population
As many patients as investigators can collect
Description
Inclusion Criteria:
- patients with diagnosed periodontitis
Exclusion Criteria:
- compromised systematic health (uncontrolled hypertension, diabetes, impaired bone metabolism condition, etc.), uncontrolled periodontal disease, smoking > 20 cigarettes/day or recent chemotherapy/radiotherapy in the oral and maxillofacial regions
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
probing depth
Time Frame: 3 years
|
the probing depth of buccal and palatal sites of teeth in one patient
|
3 years
|
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 (Estimated)
October 1, 2023
Primary Completion (Estimated)
October 1, 2024
Study Completion (Estimated)
December 31, 2025
Study Registration Dates
First Submitted
September 4, 2023
First Submitted That Met QC Criteria
September 4, 2023
First Posted (Actual)
September 11, 2023
Study Record Updates
Last Update Posted (Actual)
September 11, 2023
Last Update Submitted That Met QC Criteria
September 4, 2023
Last Verified
September 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2021-116
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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