Occlusal AnalysisNCT07860684
Clinical Assessment of Dynamic and Static Occlusal Contacts in Direct and Indirect Posterior Restorations
An observational study of Occlusal Analysis, run by Marmara University at 1 site in Turkey (Türkiye).
Trial summary
Conventional clinical evaluation of dental occlusion relies predominantly on qualitative indicators such as articulating papers, metallic foils, and silicone-based materials and the accuracy of these indicators may be influenced by material thickness, moisture contamination, and subjective interpretation. Read more about this study
- Who is it for?
- Ages 17 to 45 yearsHealthy volunteers can take part
- Conditions the study is for
- Occlusal Analysis
- Type of treatment
- Injection or infusion
- How many people
- 45 participants
- Where
- 1 siteTurkey (Türkiye)
- Study dates
- 3 Jun 2024to 6 Jun 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 17 to 45 years
- All sexes
- Healthy volunteers accepted
- Child, Adult
Study population: Patients aged between 17 and 45 requiring restoration of maxillary or mandibular first molar teeth were included in the study. The teeth with mesial-occlusal-distal (MOD) cavity preparation encompassing 50% of the intercuspal distance for direct restorations and overlay preparation for indirect restorations were included. The ones having asymptomatic root canal treatments were also included. Those who had caries, crowns, amalgam restorations, fractures, pathological wear, or severe periodontal problems on their maxillary or mandibular first molar teeth were excluded from the study. The patients who had active temporomandibular disorders, missing teeth, primary dentition, posterior disocclusion, posterior crossbite, and anterior openbite were also excluded. Those who were undergoing active orthodontic treatment were excluded from the study. Finally, total of 90 maxillary or mandibular first molars were selected from 45 patients. All the included patients were informed about the study.
Who may be able to join
- Sufficient cognitive ability to understand the consent process
- 17-45 years old
- Clinically healthy gingiva and periodontal tissues
Who cannot join
- Missing teeth except third molars
- Ongoing orthodontic or prosthetic treatments that may affect occlusion
- Bruxism
Trial locations and contacts
1 site in 1 country.
Turkey (Türkiye)1 site
Marmara University Faculty of Dentistry
Istanbul, Maltepe, 34854
About this study
Conventional clinical evaluation of dental occlusion relies predominantly on qualitative indicators such as articulating papers, metallic foils, and silicone-based materials and the accuracy of these indicators may be influenced by material thickness, moisture contamination, and subjective interpretation. Quantitative assessment of occlusal contacts in direct and indirect posterior restorations may help clinicians to establish and maintain harmonious and proper dental occlusion. To assess the level of static and dynamic occlusal contact surfaces in direct and indirect restorations, clinically and quantitatively. Also, to compare outcomes between clinicians with two different levels of clinical experience, immediately and one month after the restorative procedures. Patients requiring restoration for maxillary or mandibular first molars were treated either with direct nanohybrid resin composite (Neo Spectra ST HV A2, Dentsply) restorations or indirect restorations using computer-aided design/computer-aided manufacturing (CAD/CAM) method with hybrid ceramic material (Cerasmart 270 HT A2, GC). The direct (n =30) and indirect (n=30) restorations of postgraduate clinicians and direct restorations (n=30) of undergraduate clinicians (5th grade) were compared immediately (T1) and one month (T2) after the restorative procedures. A single dental technician performed the digital design and the milling of all indirect restorations. Static and dynamic occlusal contact surfaces of the teeth were quantitatively assessed through the collected digital scans by an intraoral scanner (iTero Element 5D, Align), using a computer software program (ChairsideCAD 3.1, Exocad, Align), by setting contact distances to 10, 50, 100, 150, 200, 250, 300, and 350 μm, gradually. The static contacts were assessed by calculating the percentage of the occlusal contact surfaces to the entire occlusal contact surface for each restored tooth, using the ImageJ software program (National Institutes of Health). The dynamic contacts were assessed according to the presence (positive) or absence (negative), regarding 4 lateral movements of the mandibular arch (0.5, 1, 2, and 3 mm on the working side) using a virtual articulator integrated to the ChairsideCAD.
Read the detailed description
The study was conducted on patients who applied to the undergraduate and postgraduate clinics of the Department of Restorative Dentistry, Marmara University Dentistry Faculty. The number of teeth to be included in the study was determined by Statistical Power Analysis (G-Power Analysis). With 90% confidence (1-α), 85% test power (1-β), and an effect size of f =0.276, the total number of teeth to be included in the study for 3 groups was determined to be a minimum of 90. Patients aged between 17 and 45 requiring restoration of maxillary or mandibular first molar teeth were included in the study. The teeth with mesial-occlusal-distal (MOD) cavity preparation encompassing 50% of the intercuspal distance for direct restorations and overlay preparation for indirect restorations were included. The ones having asymptomatic root canal treatments were also included. Those who had caries, crowns, amalgam restorations, fractures, pathological wear, or severe periodontal problems on their maxillary or mandibular first molar teeth were excluded from the study. The patients who had active temporomandibular disorders, missing teeth, primary dentition, posterior disocclusion, posterior crossbite, and anterior openbite were also excluded. Those who were undergoing active orthodontic treatment were excluded from the study. Finally, total of 90 maxillary or mandibular first molars were selected from 45 patients. All the included patients were informed about the study procedures and provided written informed consent before the study.
The restorations were performed using standardized equipment and techniques for the study groups either by a 5th-grade undergraduate clinician or a postgraduate clinician with 5 years of clinical experience. Three application groups were determined according to the type of posterior restoration and clinician. The postgraduate clinician performed 30 direct posterior MOD restorations and 30 indirect overlay restorations, and the undergraduate clinician performed 30 direct posterior MOD restorations.
Intraoral scans of the final direct and indirect restorations were obtained at immediately after and one month recall periods using the Element 5D intraoral scanner. To prevent any unintended change in occlusion, the dental procedures were prohibited for the patients between the first and second intraoral scans. For each patient, full maxillary and mandibular arches and the interocclusal records were scanned and recorded by the postgraduate clinician, and the acquired scan data were exported as polygon file format (.PLY). Then 3D digital models of the jaws were transferred to a specific software program (ChairsideCAD 3.1, Exocad, Align), in which the static and dynamic occlusal contacts with the opposing dentition could be visualized. To evaluate static and dynamic occlusal contacts, two different methods were followed.
For static occlusal contacts, after importing .PLY files into ChairsideCAD software program, the tightness of the occlusal contact surfaces was visualized and evaluated by eight occlusal distance grades: 10, 50, 100, 150, 200, 250, 300, and 350 μm. High resolution .PNG images of upper or lower jaws' 3D models were generated from the occlusal plane when the entire occlusal surface and occlusal contact areas were visible. Therefore, 8 different 2D images representing each grade were recorded in high-resolution of 90 teeth immediately after the restorations and one month after the restorations.
For the dynamic occlusal contact surface evaluation, .PLY files were imported to ChairsideCAD 3.1 software program, then 3D models were mounted on a fully adjustable Arcon type virtual articulator (Artex CR, Amann Girrbach) integrated with the software. For the mounting of the maxillary arch model to the articulator, the mesio-incisal embrasure of the upper central teeth and the mesio-buccal tubercle of the left and right upper first molars were selected respectively. The virtual articulator was adjusted to the average value parameters: Bennett angle was set at 10 degrees, immediate side shift was set at 0.5 mm, condylar angle was set at 30 degrees, and incisal table angle was set at 30 degrees as described in a previous research. In the articulator tool of the software program, the lateral movements of 0.5, 1, 2, and 3 mm were set gradually to the working side. The tightness of the occlusal contact surfaces was defined by the same occlusal distances as in static occlusal contacts (10, 50, 100, 150, 200, 250, 300, and 350 µm). The occlusal surface dynamic contacts were assessed as positive (+) or negative (-) for each lateral movement step, for all occlusal distances, immediately after the restorations and one month after the restorations.
- Conditions
- Occlusal Analysis
- Keywords
- Occlusal contact, Posterior restoration, Direct, Indirect
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
| Study group | Role | What they receive |
|---|---|---|
| Postgraduate indirect restoration group | All indirect restorations were single visit, overlay cad/cam restorations using hybrid ceramic blocks (Cerasmart 270 HT A2, GC). Selected maxillary and mandibular vital teeth or teeth with root canal treatment were restored. Non-retentive overlay preparations were performed by the clinicians. Marginal elevation was performed when necessary, using a highly filled flowable composite (Gaenial Universal Injectable A2 shade, GC) and partial precontoured matrix bands (Tor VM). No periodontal surgery, gingival retraction method, or rubber dam isolation was used before the restorations. The immediate dentin sealing procedure was performed for the vital teeth. | |
| Postgraduate direct restoration group | The direct posterior MOD restorations on maxillary and mandibular vital teeth or teeth with root canal treatment were performed by the postgraduate clinicians using a nanoceramic resin composite (Neo Spectra ST HV A2, Dentsply). MOD cavities were prepared without bevels. Following the successful adaptation of precontoured matrix bands (0.050 mm thickness, Tor VM) and wooden wedges to the mesial and distal margins of the cavities, selective enamel etching was applied. Then a universal adhesive agent (G-Premio Bond, GC) was applied according to the manufacturer's instructions. The composite was layered incrementally by starting to shape both marginal walls and then the rest was performed using the cusp-to-cusp technique. Each layer was cured by a calibrated LED curing unit (Elipar Deepcure S, 3M ESPE) for 10 seconds. | |
| Undergraduate direct restoration group | The direct posterior MOD restorations on maxillary and mandibular vital teeth or teeth with root canal treatment were performed by the undergraduate clinicians using a nanoceramic resin composite (Neo Spectra ST HV A2, Dentsply) with the same clinical protocol. MOD cavities were prepared without bevels. Following the successful adaptation of precontoured matrix bands (0.050 mm thickness, Tor VM) and wooden wedges to the mesial and distal margins of the cavities, selective enamel etching was applied. Then a universal adhesive agent (G-Premio Bond, GC) was applied according to the manufacturer's instructions. The composite was layered incrementally by starting to shape both marginal walls and then the rest was performed using the cusp-to-cusp technique. Each layer was cured by a calibrated LED curing unit (Elipar Deepcure S, 3M ESPE) for 10 seconds. |
What is being measured
The primary outcome is the main question the study is designed to answer.
Assessment of the level of static occlusal area percentage and dynamic occlusal contact presence of direct and indirect restorations, using ChairsideCAD and imageJ softwares.
Measurements of the level of static and dynamic occlusal contacts for differences of direct and indirect restoration types. Static occlusal contact areas were calculated as ratio of tooth contact area to total occlusal area. Dynamic occlusal contacts were calculated as presence.
Measured: Immediately after and 1 month follow-up
Secondary outcomes (1)
Assessment of the clinical experience factor regarding the occlusal contact levels for direct restorations for both static occlusal contact area and dynamic occlusal contact presence, using ChairsideCAD and imageJ softwares.
Measurement of clinical experience factor regarding the occlusal contact level differences of direct postgraduate and direct undergraduate restorations. Static occlusal contact areas were calculated as ratio of tooth contact area to total occlusal area. Dynamic occlusal contacts were calculated as presence.
Measured: Immediately after and 1 month follow-up
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 Oct 2026
- Study start3 Jun 2024
- Primary completion13 Jan 2025
- Study completion6 Jun 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Occlusal AnalysisStudies of the same condition, open and under way.
- More trials run by Marmara UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Case-control
- Time perspective
- Retrospective
- Enrolment
- 45 participants (actual)
Sponsor and investigators
- Lead sponsor
- Marmara University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07860684
- Sponsor's protocol ID
- 09.2024.727
- Status last verified
- Sep 2026
- First submitted
- 30 Sep 2026
- Last updated
- 13 Oct 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: All data obtained without working will be shared if requested.
Study at a glance
From the registry record, last updated by the sponsor on 13 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Clinical Assessment of Dynamic and Static Occlusal Contacts in Direct and Indirect Posterior Restorations
- ClinicalTrials.gov ID
- NCT07860684
- Acronym / sponsor ID
- 09.2024.727
- Conditions
- Occlusal Analysis
- Keywords
- Occlusal contact, Posterior restoration, Direct, Indirect
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 45 participants (actual)
- Lead sponsor
- Marmara UniversityUniversity, hospital or other
- Study start
- 3 Jun 2024 (actual)
- Primary completion
- 13 Jan 2025 (actual)
- Study completion
- 6 Jun 2025 (actual)
- First posted
- 6 Oct 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Conventional clinical evaluation of dental occlusion relies predominantly on qualitative indicators such as articulating papers, metallic foils, and silicone-based materials and the accuracy of these indicators may be influenced by material thickness, moisture contamination, and subjective interpretation. Quantitative assessment of occlusal contacts in direct and indirect posterior restorations may help clinicians to establish and maintain harmonious and proper dental occlusion. To assess the level of static and dynamic occlusal contact surfaces in direct and indirect restorations, clinically and quantitatively. Also, to compare outcomes between clinicians with two different levels of clinical experience, immediately and one month after the restorative procedures. Patients requiring restoration for maxillary or mandibular first molars were treated either with direct nanohybrid resin composite (Neo Spectra ST HV A2, Dentsply) restorations or indirect restorations using computer-aided design/computer-aided manufacturing (CAD/CAM) method with hybrid ceramic material (Cerasmart 270 HT A2, GC). The direct (n =30) and indirect (n=30) restorations of postgraduate clinicians and direct restorations (n=30) of undergraduate clinicians (5th grade) were compared immediately (T1) and one month (T2) after the restorative procedures. A single dental technician performed the digital design and the milling of all indirect restorations. Static and dynamic occlusal contact surfaces of the teeth were quantitatively assessed through the collected digital scans by an intraoral scanner (iTero Element 5D, Align), using a computer software program (ChairsideCAD 3.1, Exocad, Align), by setting contact distances to 10, 50, 100, 150, 200, 250, 300, and 350 μm, gradually. The static contacts were assessed by calculating the percentage of the occlusal contact surfaces to the entire occlusal contact surface for each restored tooth, using the ImageJ software program (National Institutes of Health). The dynamic contacts were assessed according to the presence (positive) or absence (negative), regarding 4 lateral movements of the mandibular arch (0.5, 1, 2, and 3 mm on the working side) using a virtual articulator integrated to the ChairsideCAD.
Detailed description
The study was conducted on patients who applied to the undergraduate and postgraduate clinics of the Department of Restorative Dentistry, Marmara University Dentistry Faculty. The number of teeth to be included in the study was determined by Statistical Power Analysis (G-Power Analysis). With 90% confidence (1-α), 85% test power (1-β), and an effect size of f =0.276, the total number of teeth to be included in the study for 3 groups was determined to be a minimum of 90. Patients aged between 17 and 45 requiring restoration of maxillary or mandibular first molar teeth were included in the study. The teeth with mesial-occlusal-distal (MOD) cavity preparation encompassing 50% of the intercuspal distance for direct restorations and overlay preparation for indirect restorations were included. The ones having asymptomatic root canal treatments were also included. Those who had caries, crowns, amalgam restorations, fractures, pathological wear, or severe periodontal problems on their maxillary or mandibular first molar teeth were excluded from the study. The patients who had active temporomandibular disorders, missing teeth, primary dentition, posterior disocclusion, posterior crossbite, and anterior openbite were also excluded. Those who were undergoing active orthodontic treatment were excluded from the study. Finally, total of 90 maxillary or mandibular first molars were selected from 45 patients. All the included patients were informed about the study procedures and provided written informed consent before the study.
The restorations were performed using standardized equipment and techniques for the study groups either by a 5th-grade undergraduate clinician or a postgraduate clinician with 5 years of clinical experience. Three application groups were determined according to the type of posterior restoration and clinician. The postgraduate clinician performed 30 direct posterior MOD restorations and 30 indirect overlay restorations, and the undergraduate clinician performed 30 direct posterior MOD restorations.
Intraoral scans of the final direct and indirect restorations were obtained at immediately after and one month recall periods using the Element 5D intraoral scanner. To prevent any unintended change in occlusion, the dental procedures were prohibited for the patients between the first and second intraoral scans. For each patient, full maxillary and mandibular arches and the interocclusal records were scanned and recorded by the postgraduate clinician, and the acquired scan data were exported as polygon file format (.PLY). Then 3D digital models of the jaws were transferred to a specific software program (ChairsideCAD 3.1, Exocad, Align), in which the static and dynamic occlusal contacts with the opposing dentition could be visualized. To evaluate static and dynamic occlusal contacts, two different methods were followed.
For static occlusal contacts, after importing .PLY files into ChairsideCAD software program, the tightness of the occlusal contact surfaces was visualized and evaluated by eight occlusal distance grades: 10, 50, 100, 150, 200, 250, 300, and 350 μm. High resolution .PNG images of upper or lower jaws' 3D models were generated from the occlusal plane when the entire occlusal surface and occlusal contact areas were visible. Therefore, 8 different 2D images representing each grade were recorded in high-resolution of 90 teeth immediately after the restorations and one month after the restorations.
For the dynamic occlusal contact surface evaluation, .PLY files were imported to ChairsideCAD 3.1 software program, then 3D models were mounted on a fully adjustable Arcon type virtual articulator (Artex CR, Amann Girrbach) integrated with the software. For the mounting of the maxillary arch model to the articulator, the mesio-incisal embrasure of the upper central teeth and the mesio-buccal tubercle of the left and right upper first molars were selected respectively. The virtual articulator was adjusted to the average value parameters: Bennett angle was set at 10 degrees, immediate side shift was set at 0.5 mm, condylar angle was set at 30 degrees, and incisal table angle was set at 30 degrees as described in a previous research. In the articulator tool of the software program, the lateral movements of 0.5, 1, 2, and 3 mm were set gradually to the working side. The tightness of the occlusal contact surfaces was defined by the same occlusal distances as in static occlusal contacts (10, 50, 100, 150, 200, 250, 300, and 350 µm). The occlusal surface dynamic contacts were assessed as positive (+) or negative (-) for each lateral movement step, for all occlusal distances, immediately after the restorations and one month after the restorations.
Study design
- Observational model
- Case-control
- Time perspective
- Retrospective
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Postgraduate indirect restoration group | – | –All indirect restorations were single visit, overlay cad/cam restorations using hybrid ceramic blocks (Cerasmart 270 HT A2, GC). Selected maxillary and mandibular vital teeth or teeth with root canal treatment were restored. Non-retentive overlay preparations were performed by the clinicians. Marginal elevation was performed when necessary, using a highly filled flowable composite (Gaenial Universal Injectable A2 shade, GC) and partial precontoured matrix bands (Tor VM). No periodontal surgery, gingival retraction method, or rubber dam isolation was used before the restorations. The immediate dentin sealing procedure was performed for the vital teeth. |
| Postgraduate direct restoration group | – | –The direct posterior MOD restorations on maxillary and mandibular vital teeth or teeth with root canal treatment were performed by the postgraduate clinicians using a nanoceramic resin composite (Neo Spectra ST HV A2, Dentsply). MOD cavities were prepared without bevels. Following the successful adaptation of precontoured matrix bands (0.050 mm thickness, Tor VM) and wooden wedges to the mesial and distal margins of the cavities, selective enamel etching was applied. Then a universal adhesive agent (G-Premio Bond, GC) was applied according to the manufacturer's instructions. The composite was layered incrementally by starting to shape both marginal walls and then the rest was performed using the cusp-to-cusp technique. Each layer was cured by a calibrated LED curing unit (Elipar Deepcure S, 3M ESPE) for 10 seconds. |
| Undergraduate direct restoration group | – | –The direct posterior MOD restorations on maxillary and mandibular vital teeth or teeth with root canal treatment were performed by the undergraduate clinicians using a nanoceramic resin composite (Neo Spectra ST HV A2, Dentsply) with the same clinical protocol. MOD cavities were prepared without bevels. Following the successful adaptation of precontoured matrix bands (0.050 mm thickness, Tor VM) and wooden wedges to the mesial and distal margins of the cavities, selective enamel etching was applied. Then a universal adhesive agent (G-Premio Bond, GC) was applied according to the manufacturer's instructions. The composite was layered incrementally by starting to shape both marginal walls and then the rest was performed using the cusp-to-cusp technique. Each layer was cured by a calibrated LED curing unit (Elipar Deepcure S, 3M ESPE) for 10 seconds. |
Who may qualify
- Ages
- 17 to 45 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Child, Adult
- Study population
- Patients aged between 17 and 45 requiring restoration of maxillary or mandibular first molar teeth were included in the study. The teeth with mesial-occlusal-distal (MOD) cavity preparation encompassing 50% of the intercuspal distance for direct restorations and overlay preparation for indirect restorations were included. The ones having asymptomatic root canal treatments were also included. Those who had caries, crowns, amalgam restorations, fractures, pathological wear, or severe periodontal problems on their maxillary or mandibular first molar teeth were excluded from the study. The patients who had active temporomandibular disorders, missing teeth, primary dentition, posterior disocclusion, posterior crossbite, and anterior openbite were also excluded. Those who were undergoing active orthodontic treatment were excluded from the study. Finally, total of 90 maxillary or mandibular first molars were selected from 45 patients. All the included patients were informed about the study.
Key inclusion criteria (3 listed)
- Sufficient cognitive ability to understand the consent process
- 17-45 years old
- Clinically healthy gingiva and periodontal tissues
Key exclusion criteria (3 listed)
- Missing teeth except third molars
- Ongoing orthodontic or prosthetic treatments that may affect occlusion
- Bruxism
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Assessment of the level of static occlusal area percentage and dynamic occlusal contact presence of direct and indirect restorations, using ChairsideCAD and imageJ softwares.
Time frame: Immediately after and 1 month follow-up
Measurements of the level of static and dynamic occlusal contacts for differences of direct and indirect restoration types. Static occlusal contact areas were calculated as ratio of tooth contact area to total occlusal area. Dynamic occlusal contacts were calculated as presence.
1 secondary outcome
Assessment of the clinical experience factor regarding the occlusal contact levels for direct restorations for both static occlusal contact area and dynamic occlusal contact presence, using ChairsideCAD and imageJ softwares.
Time frame: Immediately after and 1 month follow-up
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Oct 2026.
- Individual participant dataSharing planned: Yes. All data obtained without working will be shared if requested.
Related trials for Occlusal Analysis
Not yet recruitingObservational study
A Case-Control Study Revealing Intraocular Microenvironment Characteristics in Patients With Ocular Diseases Based on Multi-Omics Analysis
Age- Related Macular Degeneration, Diabetic Retinopathy
Not yet recruitingObservational study
AI-Based CT Analysis of Coronary Plaque Evolution
Coronary Artery Disease
Not yet recruitingObservational study
AI-ECG Detection of Occlusion Myocardial Infarction at Emergency Department Triage (TRIACS)
Acute Coronary Syndromes, Chest Pain
Enrolling by invitationObservational study
Influencing Factors and Outcomes of DCB Angioplasty
Coronary Artery Disease
Not yet recruitingObservational study
Hemodynamic Characteristics of Peripheral Arterial Disease Using Computational Fluid Dynamics
Peripheral Arterial Disease
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Occlusal Analysis, 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 3 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 13 Oct 2026. 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?
Assessment of the level of static occlusal area percentage and dynamic occlusal contact presence of direct and indirect restorations, using ChairsideCAD and imageJ softwares. (time frame: Immediately after and 1 month follow-up). 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 13 Oct 2026.