The Prevalence of Variations in Attachment and Morphology of Labial MLF on A Sample of Adult Egyptian Population

October 30, 2022 updated by: Abeer Ali Hussein Al-Fkih, Cairo University

The Prevalence of Variations in Attachment and Morphology of Maxillary Labial Frenum on A Sample of Adult Egyptian Population

The study aims at determining the prevalence of the various types of Maxillary Labial Frenum attachment and morphology among adult Egyptian dental outpatients attending the diagnostic center at Faculty of Dentistry, Cairo University.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Detailed Description

A frenum is a fibrous band of tissue attached to the bone of the maxilla and mandible, it is frequently superficial to the muscle attachments. There are different types of frena in a normal oral cavity, most notably the maxillary labial frenum, the mandibular labial frenum, the buccal frenum and the lingual frenum. The primary function of frenum is to provide stability of the upper and lower lip. Labial frenal attachments are thin folds of mucous membrane with enclosed muscle fibers originating from orbicularis oris muscle of the upper lip that attaches at the lips to the alveolar mucosa and underlying periosteum on the middle part of the upper lip between the upper central incisors. The labial frenum has unpredictable variation in reference to size, shape, and position during different time periods of growth and development. During the growth period, it is of less clinical importance as it has the ability to decrease in size. At a younger age frenum is generally wide and thick, with time it becomes thin and small .

Abnormal frenum attachment can lead to distension of the gingival sulcus because of frenal pull causing severe periodontal pockets as there is increase plaque accumulation and gingival recession may be caused by the frenum when attached too closely to the gingival margin. It may even affect denture fit or retention. Abnormal labial frenum has also been associated with various syndromes like Ehlers-Danlos syndrome. There are different types and variations of the labial frenum, for this the frenum assessment during oral examination is important in order to avoid misdiagnosis of normal variations as abnormal frenum.

Study Type

Observational

Enrollment (Anticipated)

384

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

Study Contact Backup

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Dental patients will be recruited in a consecutive manner from the outpatient Diagnostic center, Faculty of Dentistry, Cairo University.

Description

Inclusion Criteria:

  1. Adult Egyptian patients whose age is above 18 years old.
  2. Patient consulting in the outpatient clinic
  3. Provide informed consent.

Exclusion Criteria:

  1. Patients who have had any orofacial anomalies.
  2. Trauma/injuries in the premaxillary region.
  3. History of prior orthognathic/frenal surgeries.
  4. Missing of one or both central incisors.
  5. Patient under any medication known to affect the gingiva (e.g., phenytoin).
  6. Syndromes associated with different frenal attachments:

    • Ehlers Danlos syndrome.
    • Infantile hypertrophic pyloric stenosis.
    • Holoprosencephaly.
    • Ellis van Creveld syndrome.
    • Oro facial digital syndrome.

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

  • Observational Models: Ecologic or Community
  • Time Perspectives: Cross-Sectional

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Prevalence of variations of maxillary labial frenum attachment
Time Frame: through study completion, an average of 1 year

The primary outcome of the study is the prevalence of variations of maxillary labial frenum attachment. It will be diagnosed by proper history and clinical examination.

The clinical examination will be performed, patients will be examine lying in a supine position using direct visual method on the dental unit. Under adequate light the upper lip will gently lift with the index finger and thumb of both hands. The site of attachment of frenum will be examined through direct visual examination and intraoral photographs will be also taken. The clinical classification of maxillary frenum insertion by (Mirko, Miroslav and Lubor, 1974)

through study completion, an average of 1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Morphological labial frenum variations
Time Frame: through study completion, an average of 1 year
Under adequate light the upper lip will gently lift with the index finger and thumb of both hands. The morphology of frenum will be examined through direct visual examination and intraoral photographs will be also taken. The classification of the frenum variations in morphology are eight different types, simple, persistent tectolabial, simple with appendix, simple with nodule, double frenum, frenum with nichum, bifid frenum and frenum with one or more variation of the above (Sewerin, 1971)
through study completion, an average of 1 year

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Papilla presence
Time Frame: through study completion, an average of 1 year
Assessing the positional relationship among the papilla, cementoenamel junction (CEJ) and adjacent teeth (Cardaropoli, Re and Corrente, 2004)
through study completion, an average of 1 year
Gingival Recession Depth (RD)
Time Frame: through study completion, an average of 1 year
The evaluation will be performed on both frontal and lateral sites using University of North Carolina-15 (UNC 15) probe, and a dental explorer, two variables will be considered: CEJ and cervical discrepancies. Assessment of gingival recession at both buccal and interproximal sites (Cairo et al., 2011)
through study completion, an average of 1 year
Midline diastema
Time Frame: through study completion, an average of 1 year
Visual examination to assess the presence or absence of midline diastema, the "blanch test" use to evaluate the continuity of the tissue fibres of the labial frenum through the diastema to the palatine papilla. The test is accomplished by lifting the upper lip upward and forward until the frenum is tightly stretched. If the procedure produces a blanching or change of contour in this area, the frenum is considered abnormal (Angle, 1907)
through study completion, an average of 1 year
Width of keratinized gingiva
Time Frame: through study completion, an average of 1 year
Measure at the midbuccal aspect of the tooth by University of North Carolina-15 (UNC-15) probe which is color-coded at every millimetre demarcation. The measurement will be from the gingival margin to the mucogingival junction. The mucogingival junction will be identified by the rolling technique, where in the mucosa rolled until the non-movable portion of the attached keratinized tissue is seen (Mazzocco et al., 2011)
through study completion, an average of 1 year
Plaque index
Time Frame: through study completion, an average of 1 year
Teeth in each quadrant will be dried with a blast of air, and presence of visible dental plaque and supragingival calculus will be recorded. Scores 0,1,2,3 (Silness and Löe, 1964), each of the four surfaces of the teeth (buccal, lingual, mesial and distal) is given a score from 0-3. The scores from the four areas of the tooth are added and divided by four in order to give the plaque index for the tooth with the following scores and criteria
through study completion, an average of 1 year
Bleeding on Probing
Time Frame: through study completion, an average of 1 year
Gingival bleeding will be assessed. Gentle probing of the orifice of the gingival crevice. The periodontal probe will be inserted into the gingival sulcus starting at one interproximal area and moving to the other. If bleeding occurs within 10 seconds a positive finding is recorded (Ainamo and Bay, 1975)
through study completion, an average of 1 year

Collaborators and Investigators

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

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.

Helpful Links

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)

November 10, 2022

Primary Completion (Anticipated)

January 1, 2023

Study Completion (Anticipated)

February 1, 2023

Study Registration Dates

First Submitted

October 9, 2022

First Submitted That Met QC Criteria

October 23, 2022

First Posted (Actual)

October 25, 2022

Study Record Updates

Last Update Posted (Actual)

November 1, 2022

Last Update Submitted That Met QC Criteria

October 30, 2022

Last Verified

October 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • variations in MLF

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.

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