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Esthetics, DentalNCT06280027

Effect of Midline Discrepancy and Crown Width Disporportion on Esthetics

An observational study of Esthetics, Dental, run by Marmara University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

In the web-based cross-sectional study 180 participants were included. Half of them (n = 90) were patients (laypeople) of the university clinic and the remaining half were restorative dentists and prosthodontists with similar levels of clinical experience (at least 3 years of academic training). Read more about this study

Who is it for?
Ages 18 to 70 yearsHealthy volunteers can take part
Conditions the study is for
Esthetics, Dental
What is being tested?
survey
How many people
180 participants
Where
1 siteTurkey (Türkiye)
Study dates
5 Jun 2023to 22 Dec 2023
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 70 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Half of them (n = 90) were patients (laypeople) of the university clinic and the remaining half were restorative dentists and prosthodontists with similar levels of clinical experience (at least 3 years of academic training).

Who may be able to join

  • For Group 1: Patients (laypeople) of the university clinic
  • For Group 2:
  • Restorative dentists and prosthodontists with similar levels of clinical experience (at least 3 years of academic training).

Who cannot join

  • people with mental illness

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Marmara University Faculty of Dentistry

    Istanbul, 34854

Other trials in Turkey (Türkiye)

About this study

Official title: Effect of Midline Discrepancy and Crown Width Disproportion on Perception of Smile Esthetics

In the web-based cross-sectional study 180 participants were included. Half of them (n = 90) were patients (laypeople) of the university clinic and the remaining half were restorative dentists and prosthodontists with similar levels of clinical experience (at least 3 years of academic training).

A frontal view full-face portrait image of a 25-year-old female was selected as a model for the study, with a smile exhibiting good dental alignment, a quite good midline position, and tooth size symmetry.

Read more

The original image was digitally modified by a single restorative instructor using Photoshop CC (Adobe, USA) software program. The modifications were divided into three parts. The first part was the generation of midline discrepancy at different levels. The midline was digitally moved to the right side of the patient 1 - 4 millimeters, gradually. The midline movement was performed together with the whole maxillary arch.

The second part was the generation of individual crown width disproportions. Accordingly, the mesiodistal width of the left central, lateral, and canine was digitally decreased one by one, gradually, while the width of the symmetrical teeth on the right side was simultaneously increased.

The third part was the generation of distributed crown width disproportions. Accordingly, the total mesiodistal width of the left central, lateral, and canine was equally decreased, gradually, while the total width of the symmetrical teeth on the right side was simultaneously increased.

In total, 15 images were displayed in random order to the participants including the original image. An online survey was generated to quantitatively evaluate the level of esthetic perception. Subsequently, the participants were asked to evaluate the level of smile esthetics of the presented random images, without being informed about the digital manipulations of the images. The participants were even not informed about the original image. They were expected to answer the question "How esthetic do you consider this smile?" The evaluation of each image was performed via a Visual analog scale VAS, ranging from point 0 (extremely not esthetic) to point 100 (extremely esthetic).

Read the detailed description

The web-based cross-sectional study was designed and conducted in a university clinic between June and December 2023. 180 participants were included in the study. Half of them (n = 90) were patients (laypeople) of the university clinic and the remaining half were restorative dentists and prosthodontists with similar levels of clinical experience (at least 3 years of academic training).

A frontal view full-face portrait image of a 25-year-old female was selected as a model for the study, with a smile exhibiting good dental alignment, a quite good midline position, and tooth size symmetry. A perfectly symmetrical face was not demanded for the model in this study as the human face is considered usually not symmetrical. The frontal smiling image was captured using a DSLR full-frame camera (D750, Nikon, Japan), a macro objective (105 mm VR Nikkor, Nikon), and a dual paraflash/softbox (VL400, Visico, China). The image was saved in RAW data format and named as the original image.

The original image was digitally modified by a single restorative instructor using Photoshop CC (Adobe, USA) software program. The modifications were divided into three parts. The first part was the generation of midline discrepancy at different levels. The midline was digitally moved to the right side of the patient 1 - 4 millimeters, gradually. The midline movement was performed together with the whole maxillary arch. Simultaneously, the maxillary right first molar was gradually darkened to provide a natural-like space at the right buccal corridor.

The second part was the generation of individual crown width disproportions. Accordingly, the mesiodistal width of the left central, lateral, and canine was digitally decreased one by one, gradually, while the width of the symmetrical teeth on the right side was simultaneously increased. Therefore, disproportions of 1 mm and 2 mm were digitally generated for each tooth. For instance, to achieve 1 mm of disproportion on the central incisor, the left central width was decreased by 0.5 mm, while the right central width was increased by 0.5 mm.

The third part was the generation of distributed crown width disproportions. Accordingly, the total mesiodistal width of the left central, lateral, and canine was equally decreased, gradually, while the total width of the symmetrical teeth on the right side was simultaneously increased. Therefore, the distributed disproportions of 1 - 4 mm were digitally generated for the group of teeth. For instance, to achieve 1 mm of distributed disproportion, the total width of the left central, lateral, and canine was decreased by 0.5 mm, and the total width of the anterior teeth on the right side was increased by 0.5 mm. 0.5 mm was shared equally by each tooth. Simultaneously, the maxillary right first molar was gradually darkened to provide a natural-like space at the right buccal corridor.

In total, 15 images were displayed in random order to the participants including the original image. An online survey was generated to quantitatively evaluate the level of esthetic perception. At the beginning of the survey, the participants declared their profession, age, and gender. All the images were presented to the participants on a digitally calibrated monitor (iPad Pro 12.9", Apple Inc., USA) to minimize the standardization limitations. Subsequently, the participants were asked to evaluate the level of smile esthetics of the presented random images, without being informed about the digital manipulations of the images. The participants were even not informed about the original image. They were expected to answer the question "How esthetic do you consider this smile?" The evaluation of each image was performed via a Visual analog scale VAS, ranging from point 0 (extremely not esthetic) to point 100 (extremely esthetic). The participants moved a tab on the visual analog scale to a new position, based on their subjective perception of the presented smile esthetics. The scorings were carried out during midday (10:00 AM-14:00 PM), with standardized artificial lighting conditions and without directly exposing the monitor to the sunlight. The distance between the participant and the screen was consistently 60 cm, which stands for the typical distance between two people during social contact. Each participant could complete the survey once without a time limit and was limited to performing again. A total of 180 participants completed the survey.

Being tested
survey
Keywords
Esthetics, Dental, Midline Discrepancy, Crown Width Disproportion

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • surveyOther

    An online survey was generated to quantitatively evaluate the level of esthetic perception.

Study groups in NCT06280027
Study groupRoleWhat they receive
group1patients (laypeople) of the university clinic. The inclusion criteria were age ≥18 and ≤70 years.
Receives: Other: survey
group2restorative dentists and prosthodontists with similar levels of clinical experience (at least 3 years of academic training). The inclusion criteria were age ≥18 and ≤70 years.
Receives: Other: survey

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. survey on midline discrepancy at different levels

    participants was asked to evaluate each image via a Visual analog scale VAS, ranging from point 0 (extremely not esthetic) to point 100 (extremely esthetic).

    Measured: 10 minutes

  2. survey on individual crown width disproportions

    participants was asked to evaluate each image via a Visual analog scale VAS, ranging from point 0 (extremely not esthetic) to point 100 (extremely esthetic).

    Measured: 10 minutes

  3. survey on distributed crown width disproportions

    participants was asked to evaluate each image via a Visual analog scale VAS, ranging from point 0 (extremely not esthetic) to point 100 (extremely esthetic).

    Measured: 10 minutes

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Feb 2024
  2. Study start5 Jun 2023
  3. Primary completion12 Jun 2023
  4. Study completion22 Dec 2023

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
180 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06280027
Sponsor's protocol ID
MUDHF_BK1
Status last verified
Feb 2024
First submitted
20 Feb 2024
Last updated
28 Feb 2024
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Esthetics, Dental, run by Marmara University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 28 Feb 2024. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

survey on midline discrepancy at different levels (time frame: 10 minutes). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 Feb 2024.

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