- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02822040
An Evaluation of Root Length Measurements Using Intraoral Scan and Panoramic Radiographs
September 19, 2016 updated by: Rodrigo Viecilli, DDS, PhD, Loma Linda University
An Evaluation of Root Length Measurements Using Intraoral Scan and Panoramic
This study will attempt to validate a method of estimating root length on panoramic radiograph by crown measurement on intraoral digital scans.
Study Overview
Detailed Description
Intraoral digital scans will be taken on patients who have completed orthodontic treatment, and measurements will be made on the crown dimensions.
These dimensions will then be applied onto the same teeth as seen on panoramic radiographs and a mathematical relationship will be determined for root length.
Changes in root length will be measured from initial records to treatment complete panoramic radiographs and these estimates will be compared to actual root length changes as measured in CBCT (Cone Beam Computed Tomography) records.
Study Type
Observational
Enrollment (Actual)
21
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
13 years to 55 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients who have undergone orthodontic treatment, and associated tooth movement, and have initial records directly before the initiation of treatment.
Description
Inclusion Criteria:
- Subject has initial records including CBCT scan and panoramic radiograph that are clear. Subject must have no restorations or significant loss in tooth structure in target teeth or teeth adjacent to target.
Exclusion Criteria:
- Subjects who have records that are not clear, and who are missing target teeth.
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 |
---|---|
Experimental group
All patients who have initial and final records qualify in the experimental group.
|
All patients will have an intraoral scan performed for measurements to be taken on.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in root length in mm
Time Frame: Root length will be measured at the initiation of orthodontic treatment and at an average of 24 months later.
|
Changes in root length will be calculated, starting from the initiation of orthodontic treatment to completion of treatment, at an average of 24 months.
|
Root length will be measured at the initiation of orthodontic treatment and at an average of 24 months later.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Rodrigo Viecilli, DDS, PhD, Loma Linda University
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
July 1, 2016
Primary Completion (Actual)
September 1, 2016
Study Completion (Actual)
September 1, 2016
Study Registration Dates
First Submitted
April 18, 2016
First Submitted That Met QC Criteria
June 29, 2016
First Posted (Estimate)
July 4, 2016
Study Record Updates
Last Update Posted (Estimate)
September 20, 2016
Last Update Submitted That Met QC Criteria
September 19, 2016
Last Verified
September 1, 2016
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 5160149
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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