- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06933979
Positional Changes of Mandibular Molar After Orthodontic Treatment
Changes in the Position of Mandibular Third Molar in Orthodontically Treated Patients With First Premolars Extraction
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Fayoum, Egypt, 63514
- Fayoum University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- class I malocclusion cases (0 < ANB < 4) with moderate crowding
Exclusion Criteria:
- Absence of all permanent teeth including mandibular third molars.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Assessment of mandibular third molar positional variation
Time Frame: 2 years
|
measure angles:• LA-ISL: The inward angle (towards the 2nd molar) between long axis of mandibular third molar and the inter-sigmoid line (line connecting the deepest point of the right and left sigmoid notch of the mandible). • LA-IMB: The inward angle between long axis of mandibular third molar and the inferior border of the mandible. |
2 years
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Shereen A Mahlawy, PHD, lecturer of orthodontics, faculty of dentistry, Fayoum university
- Study Director: clinical cT trial, Clinical trials.gov
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- wisdom
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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