Orthodontic Tooth MovementNCT06934161
Comparison of the Effectiveness of Innovative Techniques to Prevent Tissue Overheating During Corticotomy Using Smartphone-Based Thermography: Reticulated Surgical Guide vs Dynamic Navigation.
A study testing dynamic computer-guided Corticotomy, static computer-guided Corticotomy and smartphone-based thermography in people with Orthodontic Tooth Movement and Burn Injury, run by University of Roma La Sapienza at 1 site in Italy.
Trial summary
Objectives: The aim of the present split-mouth randomized clinical trial was to compare the effectiveness of two innovative corticotomy techniques, using reticulated static computer-guided surgery and dynamic computer-guided surgery, in terms of prevention of tissue overheating. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Orthodontic Tooth Movement, Burn Injury
- What is being tested?
- dynamic computer-guided Corticotomy, static computer-guided Corticotomy and smartphone-based thermography
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 4 participants
- Where
- 1 siteItaly
- Study dates
- 1 Oct 2024to 31 Mar 2025
- Phase
- Interventional
- 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 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- age >18 years,
- need for orthodontic treatment and request of short-term orthodontic treatment,
- good oral hygiene,
- absence of systemic and oral cavity acute infection,
- good general health.
Who cannot join
- uncontrolled systemic disease;
- syndromic patients;
- smoking habit;
- periodontal disease.
Trial locations and contacts
1 site in 1 country.
Italy1 site
Department of Oral and Maxillofacial Sciences Sapienza University of Rome
Rome, RM, 00161
About this study
Official title: Comparison of the Effectiveness of Innovative Techniques to Prevent Tissue Overheating During Corticotomy Using Smartphone-Based Thermography: Reticulated Surgical Guide vs Dynamic Navigation. A Split-mouth Randomized Pilot Clinical Trial.
Objectives:
The aim of the present split-mouth randomized clinical trial was to compare the effectiveness of two innovative corticotomy techniques, using reticulated static computer-guided surgery and dynamic computer-guided surgery, in terms of prevention of tissue overheating.
Read more
Material and Methods:
Four adult subjects requiring accelerated orthodontic treatment were enrolled. Each subject received both interventions in different quadrants. Preoperative surgical planning involved cone-beam computed tomography (CBCT) and optical scanning to superimpose DICOM and STL files. The static technique utilized a digitally designed reticulated surgical guide featuring multiple irrigation holes, while the dynamic technique employed a navigation system to provide real-time guidance. Preoperative, intraoperative and immediate postoperative tissue temperatures were recorded using an infrared smartphone camera. Statistical analyses, including Student's t-test, Mann-Whitney, and Welch tests, were performed to assess differences in thermographic measurements.
Read the detailed description
The aim of the present study was to compare the effectiveness of two innovative corticotomy techniques, using reticulated static computer-guided surgery and dynamic computer-guided surgery, in terms of prevention of tissue overheating.
The initial hypothesis was that there were no statistically significant differences between the temperatures generated during the corticotomy between the two techniques used.
The present split-mouth randomized pilot clinical trial was conducted, in accordance with the ethical principles of the Declaration of Helsinki and CONSORT guidelines at the Department of Oral and Maxillofacial Sciences of Sapienza University of Rome, from October 2024 to February 2025. The patients were informed of the content, risks and benefits of the study, and written consent was obtained. The investigation received approval from the Ethics Committee of Lazio Area 1 (no. 7782).
The eligibility criteria were: (1) age >18 years, (2) need for orthodontic treatment and request of short-term orthodontic treatment, (3) good oral hygiene, (4) absence of systemic and oral cavity acute infection, (5) good general health.
The exclusion criteria were as it follows: (1) uncontrolled systemic disease; (2) syndromic patients; (3) smoking habit; (4) periodontal disease.
Based on the inclusion criteria, 4 patients were included and treated. The quadrant of the two corticotomy techniques was randomly decided by a coin toss and carried out by people unrelated to the research. The surgical procedure was performed by a single experienced operator (MC).
In order to achieve a shorter duration of orthodontic therapies and a safe and minimally invasive procedures, computer-assisted corticotomies were planned and performed using, in the same subject but in different quadrants, reticulated static computer-guided surgery and dynamic computer-guided surgery.
Each subject, after an intraoral examination and periodontal health assessment, underwent cone-beam computed tomography (CBCT) examination of the jaws and optical scanning. DICOM (Digital Imaging and COmmunications in Medicine) and STL (Standard Triangulation Language) files were superimposed to determine appropriate sites.
CBCT images were taken using the Scanora 3Dx cone-beam device (Soredex, Tuusul, Finland) and the exposure parameters were: 10 mA, 90 kV, 10 mA, total scanning time of 15.0 seconds, effective radiation time of 4.0 seconds, voxel size of 0.2 mm, field of view limited to upper and lower jaws. The STL files were collected using the Medit i700 intraoral scanner (Medit, Seoul, South Korea).
Once the superposition was performed, the corticotomy cuts were planned for each quadrant according to the randomly assigned technique. Regardless of the assigned technique, the space between the root of each tooth was assessed, and a longitudinal axis, running parallel to each root was established. Further, the surgical cuts were planned at a distance of at least 2 mm from the papilla, penetrating through the thickness of the cortical layer entirely. The cuts were designed on the basis of the use of the OT7A piezoelectric cutting insert (Mectron, Carasco, Genoa, Italy), considering a 0.75 mm dimension of the micro-saw.
The areas treated using static computer-guided technique involved the use of reticulated surgical guides -i.e. surgical guides characterized by slots to guide the piezoelectric saw and several holes to allow irrigation - designed through the use of Implant 3D software (Media Lab Spa, Milan, Italy). The 3D STL model of the reticulated surgical guide was printed using a Zortrax Inkspire 3D printer (Zortrax S.A. w restrukturyzacji, Olsztyn, Poland) and the Raydent surgical guide resin (Zortrax S.A. w restrukturyzacji, Olsztyn, Poland).
On the other hand, areas treated by dynamic computer-guided technique involved the use of the Navident dynamic navigation system (ClaroNav Technology Inc, Toronto, Canada).
The surgical phase began by asking the patient to rinse with 0.2% chlorhexidine mouthwash for 1 minute pre-operatively and then upper and lower plexus anesthesia was performed using mepivacaine with adrenaline 1:100.000 (Molteni Farmaceutici, Scandicci, Florence, Italy). Subsequently, in order to enable the use of the dynamic navigation system, two reference pattern tags - Head tracker and Jaw tracker - were temporarily fixed on the subject, and a calibration phase began selecting, for each jaw, three reference points on the 3D reconstruction of DICOM file generated by the Navident software (ClaroNav Technology Inc, Toronto, Canada). A calibration accuracy check was performed prior to the surgical phase, ensuring acceptable deviation values of ≤0.5 mm.
At this point, a Mini2 Infrared Smartphone Camera (Hangzhou HIKMICRO Sensing Technology Co., China) was initially calibrated with the surrounding ambient temperature. This calibration phase was essential as it enabled the device's algorithm to have a reference point based on the surrounding conditions and eliminate any bias caused by varying environmental temperatures. Then, pre-operative temperatures of attached gingiva and alveolar mucosa surfaces were recorded. The measurements were registered by distinguishing, for both arches, the temperature corresponding to soft tissues from incisor region (from central incisor to homolateral canine), premolar region (first and second premolars), and molar region (first and second molars).
After that, the reticulated surgical guides were positioned, and their stability was checked. Vertical gingival incisions were made interpromiximally below the interdental papilla in the two quadrants treated with static computer-guided surgery using a number 11 scalpel blade, and corticotomy cuts were performed using the Mectron Piezosurgery White (Mectron, Carasco, Genoa, Italy) piezoelectric surgical device and OT7A piezoelectric cutting insert (Mectron, Carasco, Genoa, Italy).
For the remaining quadrants, a vertical full-thickness gingival incision, below the interdental papilla, was performed using a number 11 scalpel blade by using the dynamic system. The OT7A micro-saw was calibrated and a calibration accuracy check was executed also in this phase, and thereafter, corticotomy cuts were performed following the real-time indications of the relative position of the micro-saw as indicated by the software, following the virtual planning made in the planning phase.
During the execution of the corticotomy cuts, for each technique used, the same flow and temperature of the cooling liquid was used, and intra-operative temperatures were recorded through the infrared smartphone camera. In addition, the post-operative tissue temperatures were registered also immediately after the corticotomies were performed.
Each thermographic measurement was performed by a single calibrated operator (A.P.) , at the same distance from subjects' soft tissues (30 centimeters) during the entire surgical time.
Statistical analysis was performed using Excel (Microsoft, Redmond, Washington, USA) and the statistical software package SPSS version 27.0 (IBM Corp., New York, USA).
To reduce the risk of statistical analysis bias, a blinded statistician external to the research performed the statistical analysis.
Results were described using descriptive statistics (including mean, minimum, maximum values and standard deviations).
The Shapiro-Wilk normality test and Brown-Forsythe test were used to assess the distribution of the data and the equality of variances, respectively. Violations of the normality or equal variance assumptions were detected for certain parameters.
The Student T-test was performed for variables without violation of assumptions, while Mann-Whitney test and Welch test were carried out, respectively, for non-normal distributed data and unequal variance variables.
The level of significance was set at P ≤ 0.05.
- Conditions
- Orthodontic Tooth Movement, Burn Injury
- Being tested
- dynamic computer-guided Corticotomy, static computer-guided Corticotomy, smartphone-based thermography
- Medical subject headings
- Burns
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
dynamic computer-guided CorticotomyProcedure or surgery
corticotomy cuts were made guided by a dynamic navigation system, ensuring accuracy and reducing the risk of injuries
static computer-guided CorticotomyProcedure or surgery
corticotomy cuts were made guided by a static system (using reticulated surgical template), ensuring accuracy and reducing the risk of injuries
smartphone-based thermographyDiagnostic test
a Mini2 Infrared Smartphone Camera (Hangzhou HIKMICRO Sensing Technology Co., China) was initially calibrated with the surrounding ambient temperature. The calibration phase was essential as it enabled the device's algorithm to have a reference point based on the surrounding conditions and eliminate any bias caused by varying environmental temperatures. Then, pre-operative temperatures of attached gingiva and alveolar mucosa surfaces were recorded. The measurements were registered by distinguishing, for both arches, the temperature corresponding to soft tissues from incisor region (from central incisor to homolateral canine), premolar region (first and second premolars), and molar region (first and second molars).
| Study group | Role | What they receive |
|---|---|---|
| static computer-guided surgery | Active comparator | Not described Receives: Procedure: static computer-guided Corticotomy; Diagnostic Test: smartphone-based thermography |
| dynamic computer guided-surgery | Experimental | Not described Receives: Procedure: dynamic computer-guided Corticotomy; Diagnostic Test: smartphone-based thermography |
What is being measured
The primary outcome is the main question the study is designed to answer.
Quantitative Surface Temperature Assessment via Smartphone-Based Infrared Thermography.
The measurement, done using smartphone-based thermal camera, involves capturing standardized baseline and follow-up thermal images of defined body regions (in this case attached gingiva and oral mucosa), with temperature values recorded as the mean of three consecutive readings. The data will be further aggregated using mean and standard deviation metrics for comparative analysis over time and between study groups.
Measured: From the start to the end of the surgical treatment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Apr 2025
- Study start1 Oct 2024
- Primary completion1 Dec 2024
- Study completion31 Mar 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Orthodontic Tooth MovementStudies of the same condition, open and under way.
- More trials run by University of Roma La SapienzaThe 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Diagnosis
- Allocation
- Randomised
- Intervention model
- Single group
- Masking
- Single blind
- Who is masked
- Outcomes assessor
- Enrolment
- 4 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Roma La Sapienza
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Michele Cassetta, University of Roma La Sapienza
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06934161
- Sponsor's protocol ID
- URomLS_Thermography
- Status last verified
- Apr 2025
- First submitted
- 31 Mar 2025
- Last updated
- 18 Apr 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 18 Apr 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparison of the Effectiveness of Innovative Techniques to Prevent Tissue Overheating During Corticotomy Using Smartphone-Based Thermography: Reticulated Surgical Guide vs Dynamic Navigation. A Split-mouth Randomized Pilot Clinical Trial.
- ClinicalTrials.gov ID
- NCT06934161
- Acronym / sponsor ID
- URomLS_Thermography
- Conditions
- Orthodontic Tooth Movement, Burn Injury
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 4 participants (actual)
- Lead sponsor
- University of Roma La SapienzaUniversity, hospital or other
- Study start
- 1 Oct 2024 (actual)
- Primary completion
- 1 Dec 2024 (actual)
- Study completion
- 31 Mar 2025 (actual)
- First posted
- 18 Apr 2025 (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.
Objectives:
The aim of the present split-mouth randomized clinical trial was to compare the effectiveness of two innovative corticotomy techniques, using reticulated static computer-guided surgery and dynamic computer-guided surgery, in terms of prevention of tissue overheating.
Material and Methods:
Four adult subjects requiring accelerated orthodontic treatment were enrolled. Each subject received both interventions in different quadrants. Preoperative surgical planning involved cone-beam computed tomography (CBCT) and optical scanning to superimpose DICOM and STL files. The static technique utilized a digitally designed reticulated surgical guide featuring multiple irrigation holes, while the dynamic technique employed a navigation system to provide real-time guidance. Preoperative, intraoperative and immediate postoperative tissue temperatures were recorded using an infrared smartphone camera. Statistical analyses, including Student's t-test, Mann-Whitney, and Welch tests, were performed to assess differences in thermographic measurements.
Detailed description
The aim of the present study was to compare the effectiveness of two innovative corticotomy techniques, using reticulated static computer-guided surgery and dynamic computer-guided surgery, in terms of prevention of tissue overheating.
The initial hypothesis was that there were no statistically significant differences between the temperatures generated during the corticotomy between the two techniques used.
The present split-mouth randomized pilot clinical trial was conducted, in accordance with the ethical principles of the Declaration of Helsinki and CONSORT guidelines at the Department of Oral and Maxillofacial Sciences of Sapienza University of Rome, from October 2024 to February 2025. The patients were informed of the content, risks and benefits of the study, and written consent was obtained. The investigation received approval from the Ethics Committee of Lazio Area 1 (no. 7782).
The eligibility criteria were: (1) age >18 years, (2) need for orthodontic treatment and request of short-term orthodontic treatment, (3) good oral hygiene, (4) absence of systemic and oral cavity acute infection, (5) good general health.
The exclusion criteria were as it follows: (1) uncontrolled systemic disease; (2) syndromic patients; (3) smoking habit; (4) periodontal disease.
Based on the inclusion criteria, 4 patients were included and treated. The quadrant of the two corticotomy techniques was randomly decided by a coin toss and carried out by people unrelated to the research. The surgical procedure was performed by a single experienced operator (MC).
In order to achieve a shorter duration of orthodontic therapies and a safe and minimally invasive procedures, computer-assisted corticotomies were planned and performed using, in the same subject but in different quadrants, reticulated static computer-guided surgery and dynamic computer-guided surgery.
Each subject, after an intraoral examination and periodontal health assessment, underwent cone-beam computed tomography (CBCT) examination of the jaws and optical scanning. DICOM (Digital Imaging and COmmunications in Medicine) and STL (Standard Triangulation Language) files were superimposed to determine appropriate sites.
CBCT images were taken using the Scanora 3Dx cone-beam device (Soredex, Tuusul, Finland) and the exposure parameters were: 10 mA, 90 kV, 10 mA, total scanning time of 15.0 seconds, effective radiation time of 4.0 seconds, voxel size of 0.2 mm, field of view limited to upper and lower jaws. The STL files were collected using the Medit i700 intraoral scanner (Medit, Seoul, South Korea).
Once the superposition was performed, the corticotomy cuts were planned for each quadrant according to the randomly assigned technique. Regardless of the assigned technique, the space between the root of each tooth was assessed, and a longitudinal axis, running parallel to each root was established. Further, the surgical cuts were planned at a distance of at least 2 mm from the papilla, penetrating through the thickness of the cortical layer entirely. The cuts were designed on the basis of the use of the OT7A piezoelectric cutting insert (Mectron, Carasco, Genoa, Italy), considering a 0.75 mm dimension of the micro-saw.
The areas treated using static computer-guided technique involved the use of reticulated surgical guides -i.e. surgical guides characterized by slots to guide the piezoelectric saw and several holes to allow irrigation - designed through the use of Implant 3D software (Media Lab Spa, Milan, Italy). The 3D STL model of the reticulated surgical guide was printed using a Zortrax Inkspire 3D printer (Zortrax S.A. w restrukturyzacji, Olsztyn, Poland) and the Raydent surgical guide resin (Zortrax S.A. w restrukturyzacji, Olsztyn, Poland).
On the other hand, areas treated by dynamic computer-guided technique involved the use of the Navident dynamic navigation system (ClaroNav Technology Inc, Toronto, Canada).
The surgical phase began by asking the patient to rinse with 0.2% chlorhexidine mouthwash for 1 minute pre-operatively and then upper and lower plexus anesthesia was performed using mepivacaine with adrenaline 1:100.000 (Molteni Farmaceutici, Scandicci, Florence, Italy). Subsequently, in order to enable the use of the dynamic navigation system, two reference pattern tags - Head tracker and Jaw tracker - were temporarily fixed on the subject, and a calibration phase began selecting, for each jaw, three reference points on the 3D reconstruction of DICOM file generated by the Navident software (ClaroNav Technology Inc, Toronto, Canada). A calibration accuracy check was performed prior to the surgical phase, ensuring acceptable deviation values of ≤0.5 mm.
At this point, a Mini2 Infrared Smartphone Camera (Hangzhou HIKMICRO Sensing Technology Co., China) was initially calibrated with the surrounding ambient temperature. This calibration phase was essential as it enabled the device's algorithm to have a reference point based on the surrounding conditions and eliminate any bias caused by varying environmental temperatures. Then, pre-operative temperatures of attached gingiva and alveolar mucosa surfaces were recorded. The measurements were registered by distinguishing, for both arches, the temperature corresponding to soft tissues from incisor region (from central incisor to homolateral canine), premolar region (first and second premolars), and molar region (first and second molars).
After that, the reticulated surgical guides were positioned, and their stability was checked. Vertical gingival incisions were made interpromiximally below the interdental papilla in the two quadrants treated with static computer-guided surgery using a number 11 scalpel blade, and corticotomy cuts were performed using the Mectron Piezosurgery White (Mectron, Carasco, Genoa, Italy) piezoelectric surgical device and OT7A piezoelectric cutting insert (Mectron, Carasco, Genoa, Italy).
For the remaining quadrants, a vertical full-thickness gingival incision, below the interdental papilla, was performed using a number 11 scalpel blade by using the dynamic system. The OT7A micro-saw was calibrated and a calibration accuracy check was executed also in this phase, and thereafter, corticotomy cuts were performed following the real-time indications of the relative position of the micro-saw as indicated by the software, following the virtual planning made in the planning phase.
During the execution of the corticotomy cuts, for each technique used, the same flow and temperature of the cooling liquid was used, and intra-operative temperatures were recorded through the infrared smartphone camera. In addition, the post-operative tissue temperatures were registered also immediately after the corticotomies were performed.
Each thermographic measurement was performed by a single calibrated operator (A.P.) , at the same distance from subjects' soft tissues (30 centimeters) during the entire surgical time.
Statistical analysis was performed using Excel (Microsoft, Redmond, Washington, USA) and the statistical software package SPSS version 27.0 (IBM Corp., New York, USA).
To reduce the risk of statistical analysis bias, a blinded statistician external to the research performed the statistical analysis.
Results were described using descriptive statistics (including mean, minimum, maximum values and standard deviations).
The Shapiro-Wilk normality test and Brown-Forsythe test were used to assess the distribution of the data and the equality of variances, respectively. Violations of the normality or equal variance assumptions were detected for certain parameters.
The Student T-test was performed for variables without violation of assumptions, while Mann-Whitney test and Welch test were carried out, respectively, for non-normal distributed data and unequal variance variables.
The level of significance was set at P ≤ 0.05.
Study design
- Primary purpose
- Diagnosis
- Allocation
- Randomised
- Intervention model
- Single group
- Masking
- Single blind (outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| static computer-guided surgery | Active comparator | Procedure: static computer-guided Corticotomy, Diagnostic Test: smartphone-based thermography |
| dynamic computer guided-surgery | Experimental | Procedure: dynamic computer-guided Corticotomy, Diagnostic Test: smartphone-based thermography |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- age >18 years,
- need for orthodontic treatment and request of short-term orthodontic treatment,
- good oral hygiene,
- absence of systemic and oral cavity acute infection,
- good general health.
Key exclusion criteria (4 listed)
- uncontrolled systemic disease;
- syndromic patients;
- smoking habit;
- periodontal disease.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| dynamic computer-guided Corticotomycorticotomy cuts were made guided by a dynamic navigation system, ensuring accuracy and reducing the risk of injuries | Procedure or surgery | dynamic computer guided-surgery |
| static computer-guided Corticotomycorticotomy cuts were made guided by a static system (using reticulated surgical template), ensuring accuracy and reducing the risk of injuries | Procedure or surgery | static computer-guided surgery |
| smartphone-based thermographya Mini2 Infrared Smartphone Camera (Hangzhou HIKMICRO Sensing Technology Co., China) was initially calibrated with the surrounding ambient temperature. The calibration phase was essential as it enabled the device's algorithm to have a reference point based on the surrounding conditions and eliminate any bias caused by varying environmental temperatures. Then, pre-operative temperatures of attached gingiva and alveolar mucosa surfaces were recorded. The measurements were registered by distinguishing, for both arches, the temperature corresponding to soft tissues from incisor region (from central incisor to homolateral canine), premolar region (first and second premolars), and molar region (first and second molars). | Diagnostic test | dynamic computer guided-surgery, static computer-guided surgery |
Primary outcome
Quantitative Surface Temperature Assessment via Smartphone-Based Infrared Thermography.
Time frame: From the start to the end of the surgical treatment
The measurement, done using smartphone-based thermal camera, involves capturing standardized baseline and follow-up thermal images of defined body regions (in this case attached gingiva and oral mucosa), with temperature values recorded as the mean of three consecutive readings. The data will be further aggregated using mean and standard deviation metrics for comparative analysis over time and between study groups.
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 18 Apr 2025.
- Individual participant dataSharing planned: No
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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?
A study testing dynamic computer-guided Corticotomy, static computer-guided Corticotomy and smartphone-based thermography in people with Orthodontic Tooth Movement and Burn Injury, run by University of Roma La Sapienza at 1 site in Italy.
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 5 inclusion and 4 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 18 Apr 2025. 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 Italy. 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?
Quantitative Surface Temperature Assessment via Smartphone-Based Infrared Thermography. (time frame: From the start to the end of the surgical treatment). 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 18 Apr 2025.