- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04244903
Prevalence of MLFA Types and MD in Egyptian Children With Erupted Canines (diastema)
June 1, 2022 updated by: Asmaa Ahmed Saad, Cairo University
Prevalence of Maxillary Labial Frenal Attachments Types and Midline Diastema in Egyptian Children With Fully Erupted Maxillary Permanent Canines
Descriptive observational cross sectional study Outpatient at faculty of dentistry Cairo university pediatric dentistry department clinic with midline diastema and fully erupted canines will be examined and assess type of frenal attachment to see if correlation present or not
Study Overview
Status
Recruiting
Conditions
Study Type
Observational
Enrollment (Anticipated)
275
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: 33,saad ibn aby waqas street, faisal, giza
- Phone Number: 01014007249
- Email: Asmaa_saad@dentistry.cu.edu.eg
Study Contact Backup
- Name: 33,saad ibn aby waqas street, faisal, giza
- Phone Number: 01004541979
- Email: Wael.mustafa@dentistry.cu.edu.eg
Study Locations
-
-
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Giza, Egypt
- Enrolling by invitation
- Asmaa Ahmed saad
-
-
Giza
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Cairo, Giza, Egypt
- Recruiting
- Faculty of dentistry cairo university
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Contact:
- Asmaa Saad, Master
- Phone Number: 01014007249
- Email: asmaa_saad@dentistry.cu.edu.eg
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-
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
9 years to 13 years (Child)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
This study will be conducted among Egyptian children with fully erupted canines, who regularly attend the outpatient clinic of pediatric dentistry department, Cairo University.
Description
Inclusion Criteria:
- Systemically healthy children
- Egyptian children with fully erupted canines
- Patient presented for routine evaluation or treatment
Exclusion Criteria:
- Children who exhibited congenital anomalies or orofacial defects
- Children with previous trauma in frenal area which affect its morphology
- Children have previous surgical intervention in labial frenum or in the maxillary anterior region.
- Children have any syndromes or habits that affect the anterior maxillary region.
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 |
---|---|---|
Incidence of Midline diastema
Time Frame: 1 year
|
measuring diastema in millimeters using calibrated ruler
|
1 year
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Frenal attachment types
Time Frame: 1 year
|
Direct visual method
|
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 (Anticipated)
June 1, 2022
Primary Completion (Anticipated)
June 1, 2022
Study Completion (Anticipated)
August 1, 2022
Study Registration Dates
First Submitted
January 25, 2020
First Submitted That Met QC Criteria
January 25, 2020
First Posted (Actual)
January 28, 2020
Study Record Updates
Last Update Posted (Actual)
June 2, 2022
Last Update Submitted That Met QC Criteria
June 1, 2022
Last Verified
June 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CEBD-CU-2019-12-05
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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