AzTrials
AzTrials

Maxillary RetrusionNCT07133503

Radiological Evaluation of Anterior Maxilla For Immediate Implant Placement

An observational study of Maxillary Retrusion, run by TC Erciyes University at 2 sites in Turkey (Türkiye).

Completed

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

Official record
Search all trials

Trial summary

According to the literature age and gender may be associated with differences in skeletal size, anatomy and architecture in humans. However, little is known about the synergistic effects of age and gender on the healing capacity of maxillary bones, since most of the preclinical studies are focused on each variable… Read more about this study

Who is it for?
Ages 20 to 80 yearsHealthy volunteers can take part
Conditions the study is for
Maxillary Retrusion
What is being tested?
radiological evaluation
How many people
278 participants
Where
2 sitesTurkey (Türkiye)
Study dates
1 Jan 2024to 1 May 2025
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 20 to 80 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Cone-beam coemputed tomography (CBCT) images of individuals, obtained for various diagnostic purposes at the Erciyes University Faculty of Dentistry, Oral and Maxillofacial Radiology Clinic between January 2015 and January 2024

Who may be able to join

  • -Between January 2015 and January 2024, undergoing CBCT imaging at the Erciyes University Faculty of Dentistry, Department of Oral and Maxillofacial Radiology

Who cannot join

  • Systemic diseases,
  • Anterior maxillary tooth loss,
  • Having root canal treatments,
  • Periapical lesions,
  • History of or ongoing periodontal disease,
  • Smoking.

Trial locations and contacts

2 sites in 1 country.

Turkey (Türkiye)2 sites
  • Erciyes University Faculty of Dentistry Department of Periodontology

    Kayseri, Kayseri̇, 38000

  • Erciyes University

    Kayseri, Melikgazi, 38000

Other trials in Turkey (Türkiye)

About this study

Official title: Evaluation of Buccal Bone Thickness, Ridge Dimensions, And Root Position In Anterior Maxilla For Immediate Implant Placement

According to the literature age and gender may be associated with differences in skeletal size, anatomy and architecture in humans. However, little is known about the synergistic effects of age and gender on the healing capacity of maxillary bones, since most of the preclinical studies are focused on each variable separately. The present study radiologically evaluated various parameters such as alveolar crest height and width, buccal bone thickness, degree of buccal undercut, and root-crest angle using cone-beam computed tomography (CBCT) in a large patient population, and compared these parameters across different age and gender groups to analyze the effect of aging and gender on the bone morphology in the anterior maxillary region.

Read the detailed description

Aim: The aim of this present study was to radiologically evaluate the socket morphology that may have a clinical impact on the outcomes of immediate implant placement in the anterior maxilla, using cone-beam computed tomography (CBCT) in a large patient population. Moreover, the parameters were compared between different age and gender groups to analyze the effect of aging and gender on the bone morphology around the maxillary anterior teeth.

Material and Methods: This study evaluated a total of 1,668 teeth in the esthetic region, including bilateral central incisors, lateral incisors, and canines in the upper anterior region, using CBCT images from 278 individuals. CBCT images were grouped into age ranges of 20-29, 30-39, 40-49, 50-59, 60-69, and 70-80 years. The morphology of the anterior ridge was assessed by separately measuring alveolar ridge width and height, buccal bone thickness, tooth-crest angle, and buccal undercut for maxillary central incisors.

Being tested
radiological evaluation
Keywords
Immediate implant applications, Cone-beam computed tomography, Anterior maxilla, Alveolar ridge morphology, Aging
Medical subject headings
Retrognathia

What participants receive

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

  • radiological evaluationOther

    Using a line drawn through the midpoints of the teeth, parallel to their long axes, the anterior crest morphology was assessed. For maxillary central, lateral, and canine teeth, alveolar crest width and height, buccal bone thickness, and tooth-crest angle were measured separately. To determine buccal bone thickness, measurements were taken from the buccal crest apex, the midpoint of the root, and the apex of the tooth. The height of the alveolar crest was defined as the length of a line drawn parallel to the crest's long axis between the nasal fossa floor and the alveolar crest. The width of the alveolar crest was calculated by averaging measurements taken from the midpoints of three equal sections of the alveolar crest. The buccal undercut was determined as the point where the crest came closest to the root in the sagittal plane. Additionally, the angle between the tooth roots and the alveolar crest was measured to determine the root position in the radial plane

Study groups in NCT07133503
Study groupRoleWhat they receive
20-29 age groupIn this age group bilateral central incisors, lateral incisors, and canines in the upper anterior region were examined
Receives: Other: radiological evaluation
30-39 age groupIn this age group bilateral central incisors, lateral incisors, and canines in the upper anterior region were examined
Receives: Other: radiological evaluation
40-49 age groupIn this age group bilateral central incisors, lateral incisors, and canines in the upper anterior region were examined
Receives: Other: radiological evaluation
50-59 age groupIn this age group bilateral central incisors, lateral incisors, and canines in the upper anterior region were examined
Receives: Other: radiological evaluation
60-69 age groupIn this age group bilateral central incisors, lateral incisors, and canines in the upper anterior region were examined
Receives: Other: radiological evaluation
70-80 age groupIn this age group bilateral central incisors, lateral incisors, and canines in the upper anterior region were examined
Receives: Other: radiological evaluation

What is being measured

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

  1. Alveolar Crest Height

    The height of the alveolar crest was defined as the length of a line drawn parallel to the crest's long axis between the nasal fossa floor and the alveolar crest.

    Measured: One year

  2. Alveolar Crest Width

    The width of the alveolar crest was calculated by averaging measurements taken from the midpoints of three equal sections of the alveolar crest.

    Measured: One year

  3. Buccal Bone Thickness

    To determine buccal bone thickness, measurements were taken from the buccal crest apex, the midpoint of the root, and the apex of the tooth.

    Measured: One year

  4. Buccal Undercut Depth

    The buccal undercut was determined as the point where the crest came closest to the root in the sagittal plane.

    Measured: One year

  5. Root Position

    the angle between the tooth roots and the alveolar crest was measured to determine the root position in the radial plane

    Measured: One year

Timeline

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

  1. First posted21 Aug 2025
  2. Study start1 Jan 2024
  3. Primary completion1 Jan 2025
  4. Study completion1 May 2025

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
Other
Time perspective
Cross-sectional
Enrolment
278 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07133503
Sponsor's protocol ID
EU2020/470
Status last verified
Aug 2025
First submitted
22 Jul 2025
Last updated
21 Aug 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Maxillary Retrusion, run by TC Erciyes University at 2 sites 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 1 inclusion and 6 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 21 Aug 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites 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?

Alveolar Crest Height (time frame: One year). The study lists 5 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 21 Aug 2025.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in