A Retrospective Cone Beam Computed Tomography Study of The Lateral Wall Bony Window

March 7, 2024 updated by: The Dental Hospital of Zhejiang University School of Medicine
Three experienced observers were asked to screen all the CBCT images from the Stomatology Hospital,Zhejiang University School of Medicine, between September 1, 2019 and December 31, 2019, and counted 1000 maxillary sinus CBCT images that met the criteria. Later, 1000 CBCT images were further measured and analyzed, and indicators such as maxillary sinus buccal wall thickness, morphology, whether there is blood vessel or not, whether there is bone septa or not were counted. The variation rules and related factors were summarized by SPSS analysis.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

1000

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

  • China
    • Zhejiang
      • Hangzhou, Zhejiang, China, 310000
        • Stomatology Hospital, School 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

Yes

Sampling Method

Non-Probability Sample

Study Population

edentulous ridges in the bilateral posterior maxillary area in Chinese patients

Description

Inclusion Criteria:

  • Images were included if the following criteria were met: (1) patients were 18 years or older, (2) presence of teeth adjacent to or opposing the edentulous area allowing the location of the edentulous ridges corresponding to the tooth site to be identified, (3) presence of maxillary dentition defect in any tooth positon of the second premolar, the first molar or the second molar, (4) the maxillary sinus to be measured was visible from its floor to at least 15 mm high.

Exclusion Criteria:

  • Images were excluded if any of the following criteria were met: (1) images were unclear or incomplete due to scattering or other reasons, (2) pristine maxillary posterior extraction sites after less than 3 months of healing and the tooth extraction sockets could be obviously identified, (3) the maxillary sinus had been grafted for implant-supported prosthesis, (4) implants or other prosthetic devices were present in maxillary posterior edentulous position, (5) orthodontic brackets and wires in images were present; (6) the location of the edentulous sites could not be determined, (7) sinus pathology was present that made the measurement impossible.

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
cross-sectional
To analyze the maxillary sinus anatomy over edentulous ridges in the bilateral posterior maxillary area in Chinese patients using cone-beam computed tomography (CBCT).
Other: No intervention
Just observation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Lateral wall thickness
Time Frame: 2019-09-01~2019-12-31
The thickness of the maxillary sinus lateral wall
2019-09-01~2019-12-31

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

The Dental Hospital of Zhejiang University School of Medicine

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

September 1, 2019

Primary Completion (Actual)

January 1, 2020

Study Completion (Actual)

December 31, 2020

Study Registration Dates

First Submitted

March 7, 2024

First Submitted That Met QC Criteria

March 7, 2024

First Posted (Actual)

March 13, 2024

Study Record Updates

Last Update Posted (Actual)

March 13, 2024

Last Update Submitted That Met QC Criteria

March 7, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • JXHU

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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.

Clinical Trials on Lateral Wall Thickness

Clinical Trials on No intervention

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Qatar

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

Subscribe