Dental CrowdingNCT07821723
Clear Aligners With Two Different Change Schedules vs Traditional Braces for People With Crowded Lower Front Teeth
A study testing Clear aligner, 0.25 mm per step, Clear aligner, 0.35 mm per step and Conventional fixed orthodontic appliance in people with Dental Crowding and Malocclusion, run by Ain Shams University at 1 site in Egypt.
Trial summary
The goal of this clinical trial was to compare two clear aligner treatment plans with traditional braces for treating crowded lower front teeth in adults. Clear aligners were removable plastic trays. Traditional braces were metal brackets and wires. Read more about this study
- Who is it for?
- Ages 18 to 40 years
- Conditions the study is for
- Dental Crowding, Malocclusion
- What is being tested?
- Clear aligner, 0.25 mm per step, Clear aligner, 0.35 mm per step and Conventional fixed orthodontic appliance
- Type of treatment
- Pill or oral medicine, Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 21 participants
- Where
- 1 siteEgypt
- Study dates
- 12 Oct 2022to 20 May 2024
- 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 to 40 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- Age 18 to 40 years
- Non-extraction treatment plan
- Little's Irregularity Index (LII) ≥ 4 mm
- Presence of permanent dentition from first molar to first molar
- Absence of supernumerary teeth or tooth shape anomalies
Who cannot join
- History of prior orthodontic treatment
- Systemic pathologies
- Ongoing use of medications known to influence tooth movement (e.g., prostaglandin inhibitors, bisphosphonates)
- Active periodontal disease
- Belonging to vulnerable populations
Trial locations and contacts
1 site in 1 country.
Egypt1 site
Faculty of Dentistry, Ain Shams University, Cairo University, Cairo, Egypt
Cairo, 0020
About this study
Official title: Comparison Between Two Clear Aligner Activation Increments and Conventional Orthodontic Fixed Appliance in Treatment of Lower Incisors Crowding: A Randomized Clinical Trial
The goal of this clinical trial was to compare two clear aligner treatment plans with traditional braces for treating crowded lower front teeth in adults. Clear aligners were removable plastic trays. Traditional braces were metal brackets and wires.
The main questions the study aimed to answer were:
Read more
How fast did the teeth move?
How long did treatment take?
How much pain did participants feel?
Researchers studied 21 adults aged 18 to 40 years. The adults had mild to moderate crowding of the lower front teeth. They did not have teeth removed for treatment. Researchers assigned participants by chance to one of three groups:
Aligner I: clear aligners that moved teeth 0.25 mm per step.
Aligner II: clear aligners that moved teeth 0.35 mm per step.
Control: traditional braces.
Participants:
Wore clear aligners for 22 hours a day and changed to a new aligner every 2 weeks, or wore traditional braces that were adjusted every month.
Visited the clinic for checkups, tooth scans, and pain checks.
Were treated for up to 20 weeks.
Researchers measured crowding with a score that showed how crooked the lower front teeth were. They recorded how many weeks treatment took. They asked participants to rate pain on a 0 to 10 scale. A score of 0 meant no pain. A score of 10 meant the worst pain.
Researchers found that all three treatments straightened the teeth. Traditional braces worked fastest. The typical participant in the braces group finished in 10 weeks. The typical participant in Aligner II finished in 12 weeks. The typical participant in Aligner I finished in 16 weeks. Pain changed over time in all groups. Clear aligners were not always more comfortable than braces. At weeks 8 and 10, both aligner groups reported more pain than the braces group.
Read the detailed description
This study was a three-arm, parallel-group, randomized clinical trial conducted at the outpatient clinic of the Orthodontics Department, Faculty of Dentistry, Ain Shams University. Twenty-one participants were enrolled and allocated equally to three groups (n = 7 per group) using simple randomization. An allocation sequence was generated with Microsoft Excel by a colleague not involved in the trial. Each participant received a sequential number corresponding to presentation order, and group assignment was determined by matching this number to the pre-generated sequence.
For the aligner groups, intraoral scan datasets were imported into 3Shape software (3Shape Ortho System, 3Shape A/S, Copenhagen, Denmark). Models were spatially oriented using three reference points: the central fossae of the maxillary right and left first molars and the contact point between the central incisors. Model bases were created 4-5 mm apical to the gingival margins. Individual tooth segmentation was performed by identifying mesial and distal contact points, refining tooth splines, and adjusting axial orientation. The diagnostic setup involved adjusting the occlusal plane to reproduce any clinical canting, selecting and refining the arch form, and performing a three-dimensional tooth setup to achieve ideal alignment per American Board of Orthodontics criteria without overcorrection. Incremental staging steps were generated. Extrusive and intrusive movements were set at 0.15 mm per step; rotational, tipping, and torquing movements were set at 1 degree per step. Planar translation increments were the group-specific variable: 0.25 mm per step for Aligner I and 0.35 mm per step for Aligner II. Each staging step was inspected for interproximal or occlusal interferences exceeding 0.2 mm, which were resolved within the software. Attachments were placed according to biomechanical needs: vertical attachments for tip or rotation ≥5 degrees and horizontal attachments for extrusion ≥0.5 mm. Attachments were positioned centrally and as incisally or occlusally as possible without interfering with occlusion. Standard dimensions were 3.5 × 1.5 × 0.8 mm, with adjustments based on tooth morphology or occlusal interferences. Finalized digital models were labeled with the patient's name and exported as STL files.
For aligner fabrication, STL files were sent to a digital lab. Models were printed using Formlabs Grey resin (Formlabs, Somerville, MA, USA) on a Form 2 3D printer (Formlabs Inc., Somerville, MA, USA). Printed samples were washed in a Form Wash tank (Formlabs) for 20 minutes and post-cured in a Form Cure tank (Formlabs). Aligners were thermoformed from 0.8 mm Erkodur-AL material (Erkodent Erich Kopp GmbH, Germany) using a MiniSTAR S machine (Scheu-Dental GmbH, Iserlohn, Germany). Aligners were trimmed in a straight line terminating 2 mm apical to the gingival margins.
Clinically, one week before bonding, patients in the aligner groups received dental prophylaxis. After isolation with cheek retractors, cotton rolls, and suction, enamel surfaces were etched with 37% phosphoric acid for 15 seconds, rinsed, and dried to a frosty appearance. A thin layer of Transbond XT primer (3M Unitek, Monrovia, CA) was applied and light-cured. The attachment template was seated. Flowable composite (Nexcomp Flow, Meta Blomea, Korea) was injected into attachment recesses and light-cured through the template. The template was removed, and excess composite was finished with a carbide bur. Interproximal reduction was performed using metallic abrasive strips as prescribed. Gained space was measured using IPR gauges. Treated surfaces were polished. The first aligner was seated using chewies.
For the control group, conventional fixed appliance therapy was initiated. One week after polishing, teeth were isolated and etched with 37% phosphoric acid for 30 seconds. After rinsing and drying, Transbond XT primer was applied. Stainless steel brackets with a Roth prescription and 0.018-inch slot size, along with bondable molar tubes, were bonded using Transbond XT composite. Each bracket was firmly seated, excess adhesive was removed, and adhesive was light-cured for 20 seconds per tooth. Leveling and aligning were performed using a standardized, progressive sequence of nickel-titanium archwires, advancing to rectangular stainless-steel wires.
Statistical analysis was performed using IBM SPSS Statistics for Windows (Version 23.0, Armonk, NY: IBM Corp). Normality of numerical data was assessed through visual inspection of distributions and confirmed with Kolmogorov-Smirnov and Shapiro-Wilk tests. Because all variables exhibited non-normal distributions, non-parametric methods were used. Data were summarized as median, range, mean, and standard deviation. Intergroup comparisons among the three groups were performed using the Kruskal-Wallis test, followed by the Mann-Whitney U test for pairwise comparisons. Longitudinal changes within each group were evaluated using the Friedman test. When Kruskal-Wallis or Friedman tests yielded statistically significant results, post hoc pairwise comparisons were conducted using Dunn's test. The threshold for statistical significance was set at P ≤ 0.05.
- Conditions
- Dental Crowding, Malocclusion
- Being tested
- Clear aligner, 0.25 mm per step, Clear aligner, 0.35 mm per step, Conventional fixed orthodontic appliance
- Keywords
- Fixed orthodontic appliances, Tooth movement, Pain level, Crowding, Clear aligners
- Medical subject headings
- Crowding, Malocclusion
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Clear aligner, 0.25 mm per stepDevice
Also called Aligner I, 0.25 mm/step planar translation aligner, 0.25 mm clear aligner
Participants in this group received custom removable clear aligners designed to produce 0.25 mm of planar translation per step. Aligners were fabricated from intraoral scans using 0.8 mm Erkodur-AL material. Extrusive and intrusive movements were set at 0.15 mm per step. Rotational, tipping, and torquing movements were set at 1 degree per step. Composite attachments were placed as needed for tooth movement. Participants wore the aligners for 22 hours per day and changed to a new aligner every 2 weeks. Interproximal reduction was performed as prescribed.
Clear aligner, 0.35 mm per stepDevice
Also called Aligner II, 0.35 mm clear aligner, 0.35 mm/step planar translation aligner
Participants in this group received custom removable clear aligners designed to produce 0.35 mm of planar translation per step. Aligners were fabricated from intraoral scans using 0.8 mm Erkodur-AL material. Extrusive and intrusive movements were set at 0.15 mm per step. Rotational, tipping, and torquing movements were set at 1 degree per step. Composite attachments were placed as needed for tooth movement. Participants wore the aligners for 22 hours per day and changed to a new aligner every 2 weeks. Interproximal reduction was performed as prescribed.
Conventional fixed orthodontic applianceDevice
Also called Fixed appliance, Traditional braces, 0.018-inch Roth brackets
Participants in this group received conventional fixed orthodontic appliances. Stainless steel brackets with a Roth prescription and 0.018-inch slot size, along with bondable molar tubes, were bonded using Transbond XT composite. Leveling and aligning were performed using a standardized progressive sequence of nickel-titanium archwires, advancing to rectangular stainless-steel wires. Archwires were changed every 4 weeks based on clinical response. Participants were seen monthly for checkups.
| Study group | Role | What they receive |
|---|---|---|
| Aligner I (0.25 mm/step) | Experimental | Participants received custom removable clear aligners designed to produce 0.25 mm of planar translation per step. Aligners were fabricated from intraoral scans using 0.8 mm Erkodur-AL material. Extrusive and intrusive movements were set at 0.15 mm per step; rotational, tipping, and torquing movements at 1 degree per step. Composite attachments were placed as needed. Participants wore aligners for 22 hours per day and changed to a new aligner every 2 weeks. Interproximal reduction was performed as prescribed. Follow-up visits occurred every 2 weeks. Receives: Device: Clear aligner, 0.25 mm per step |
| Aligner II (0.35 mm/step) | Experimental | Participants received custom removable clear aligners designed to produce 0.35 mm of planar translation per step. Aligners were fabricated from intraoral scans using 0.8 mm Erkodur-AL material. Extrusive and intrusive movements were set at 0.15 mm per step; rotational, tipping, and torquing movements at 1 degree per step. Composite attachments were placed as needed. Participants wore aligners for 22 hours per day and changed to a new aligner every 2 weeks. Interproximal reduction was performed as prescribed. Follow-up visits occurred every 2 weeks. Receives: Device: Clear aligner, 0.35 mm per step |
| Control (Fixed Appliance) | Active comparator | Participants received conventional fixed orthodontic appliances. Stainless steel brackets with a Roth prescription and 0.018-inch slot size, along with bondable molar tubes, were bonded using Transbond XT composite. Leveling and aligning were performed using a standardized progressive sequence of nickel-titanium archwires, advancing to rectangular stainless-steel wires. Archwires were changed every 4 weeks based on clinical response. Participants were seen monthly for checkups. Oral hygiene was reinforced, and appliance complications were addressed. Receives: Device: Conventional fixed orthodontic appliance |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in Little's Irregularity Index (LII)
LII is a quantitative score of mandibular anterior crowding. It was measured from intraoral digital scans at baseline and at each follow-up visit using 3Shape 3D Viewer software. A lower LII indicated less crowding.
Measured: Baseline; every 2 weeks for the aligner groups and monthly for the control group; up to 20 weeks.
Secondary outcomes (2)
Pain intensity
Pain was assessed using a 10-cm Visual Analogue Scale (VAS), with scores ranging from 0 (no pain) to 10 (maximum pain). An Arabic version was administered to ensure accuracy.
Measured: Aligner groups: every 2 weeks. Control group: weekly until crowding resolution. Up to 20 weeks.
treatment duration
Number of weeks required to achieve complete alignment, defined as an LII score of 0 at the final scan.
Measured: Up to 20 weeks.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted16 Sep 2026
- Study start12 Oct 2022
- Primary completion29 Jan 2024
- Study completion20 May 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Dental CrowdingStudies of the same condition, open and under way.
- More trials run by Ain Shams 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
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 21 participants (actual)
Sponsor and investigators
- Lead sponsor
- Ain Shams University
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Sara Abozayed, Ain Shams University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07821723
- Sponsor's protocol ID
- FDASU-Rec-im012257
- Status last verified
- Sep 2026
- First submitted
- 10 Sep 2026
- Last updated
- 17 Sep 2026
- Results posted
- No
- Data monitoring committee
- No
- 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 17 Sep 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparison Between Two Clear Aligner Activation Increments and Conventional Orthodontic Fixed Appliance in Treatment of Lower Incisors Crowding: A Randomized Clinical Trial
- ClinicalTrials.gov ID
- NCT07821723
- Acronym / sponsor ID
- FDASU-Rec-im012257
- Conditions
- Dental Crowding, Malocclusion
- Keywords
- Fixed orthodontic appliances, Tooth movement, Pain level, Crowding, Clear aligners
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 21 participants (actual)
- Lead sponsor
- Ain Shams UniversityUniversity, hospital or other
- Study start
- 12 Oct 2022 (actual)
- Primary completion
- 29 Jan 2024 (actual)
- Study completion
- 20 May 2024 (actual)
- First posted
- 16 Sep 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.
The goal of this clinical trial was to compare two clear aligner treatment plans with traditional braces for treating crowded lower front teeth in adults. Clear aligners were removable plastic trays. Traditional braces were metal brackets and wires.
The main questions the study aimed to answer were:
How fast did the teeth move?
How long did treatment take?
How much pain did participants feel?
Researchers studied 21 adults aged 18 to 40 years. The adults had mild to moderate crowding of the lower front teeth. They did not have teeth removed for treatment. Researchers assigned participants by chance to one of three groups:
Aligner I: clear aligners that moved teeth 0.25 mm per step.
Aligner II: clear aligners that moved teeth 0.35 mm per step.
Control: traditional braces.
Participants:
Wore clear aligners for 22 hours a day and changed to a new aligner every 2 weeks, or wore traditional braces that were adjusted every month.
Visited the clinic for checkups, tooth scans, and pain checks.
Were treated for up to 20 weeks.
Researchers measured crowding with a score that showed how crooked the lower front teeth were. They recorded how many weeks treatment took. They asked participants to rate pain on a 0 to 10 scale. A score of 0 meant no pain. A score of 10 meant the worst pain.
Researchers found that all three treatments straightened the teeth. Traditional braces worked fastest. The typical participant in the braces group finished in 10 weeks. The typical participant in Aligner II finished in 12 weeks. The typical participant in Aligner I finished in 16 weeks. Pain changed over time in all groups. Clear aligners were not always more comfortable than braces. At weeks 8 and 10, both aligner groups reported more pain than the braces group.
Detailed description
This study was a three-arm, parallel-group, randomized clinical trial conducted at the outpatient clinic of the Orthodontics Department, Faculty of Dentistry, Ain Shams University. Twenty-one participants were enrolled and allocated equally to three groups (n = 7 per group) using simple randomization. An allocation sequence was generated with Microsoft Excel by a colleague not involved in the trial. Each participant received a sequential number corresponding to presentation order, and group assignment was determined by matching this number to the pre-generated sequence.
For the aligner groups, intraoral scan datasets were imported into 3Shape software (3Shape Ortho System, 3Shape A/S, Copenhagen, Denmark). Models were spatially oriented using three reference points: the central fossae of the maxillary right and left first molars and the contact point between the central incisors. Model bases were created 4-5 mm apical to the gingival margins. Individual tooth segmentation was performed by identifying mesial and distal contact points, refining tooth splines, and adjusting axial orientation. The diagnostic setup involved adjusting the occlusal plane to reproduce any clinical canting, selecting and refining the arch form, and performing a three-dimensional tooth setup to achieve ideal alignment per American Board of Orthodontics criteria without overcorrection. Incremental staging steps were generated. Extrusive and intrusive movements were set at 0.15 mm per step; rotational, tipping, and torquing movements were set at 1 degree per step. Planar translation increments were the group-specific variable: 0.25 mm per step for Aligner I and 0.35 mm per step for Aligner II. Each staging step was inspected for interproximal or occlusal interferences exceeding 0.2 mm, which were resolved within the software. Attachments were placed according to biomechanical needs: vertical attachments for tip or rotation ≥5 degrees and horizontal attachments for extrusion ≥0.5 mm. Attachments were positioned centrally and as incisally or occlusally as possible without interfering with occlusion. Standard dimensions were 3.5 × 1.5 × 0.8 mm, with adjustments based on tooth morphology or occlusal interferences. Finalized digital models were labeled with the patient's name and exported as STL files.
For aligner fabrication, STL files were sent to a digital lab. Models were printed using Formlabs Grey resin (Formlabs, Somerville, MA, USA) on a Form 2 3D printer (Formlabs Inc., Somerville, MA, USA). Printed samples were washed in a Form Wash tank (Formlabs) for 20 minutes and post-cured in a Form Cure tank (Formlabs). Aligners were thermoformed from 0.8 mm Erkodur-AL material (Erkodent Erich Kopp GmbH, Germany) using a MiniSTAR S machine (Scheu-Dental GmbH, Iserlohn, Germany). Aligners were trimmed in a straight line terminating 2 mm apical to the gingival margins.
Clinically, one week before bonding, patients in the aligner groups received dental prophylaxis. After isolation with cheek retractors, cotton rolls, and suction, enamel surfaces were etched with 37% phosphoric acid for 15 seconds, rinsed, and dried to a frosty appearance. A thin layer of Transbond XT primer (3M Unitek, Monrovia, CA) was applied and light-cured. The attachment template was seated. Flowable composite (Nexcomp Flow, Meta Blomea, Korea) was injected into attachment recesses and light-cured through the template. The template was removed, and excess composite was finished with a carbide bur. Interproximal reduction was performed using metallic abrasive strips as prescribed. Gained space was measured using IPR gauges. Treated surfaces were polished. The first aligner was seated using chewies.
For the control group, conventional fixed appliance therapy was initiated. One week after polishing, teeth were isolated and etched with 37% phosphoric acid for 30 seconds. After rinsing and drying, Transbond XT primer was applied. Stainless steel brackets with a Roth prescription and 0.018-inch slot size, along with bondable molar tubes, were bonded using Transbond XT composite. Each bracket was firmly seated, excess adhesive was removed, and adhesive was light-cured for 20 seconds per tooth. Leveling and aligning were performed using a standardized, progressive sequence of nickel-titanium archwires, advancing to rectangular stainless-steel wires.
Statistical analysis was performed using IBM SPSS Statistics for Windows (Version 23.0, Armonk, NY: IBM Corp). Normality of numerical data was assessed through visual inspection of distributions and confirmed with Kolmogorov-Smirnov and Shapiro-Wilk tests. Because all variables exhibited non-normal distributions, non-parametric methods were used. Data were summarized as median, range, mean, and standard deviation. Intergroup comparisons among the three groups were performed using the Kruskal-Wallis test, followed by the Mann-Whitney U test for pairwise comparisons. Longitudinal changes within each group were evaluated using the Friedman test. When Kruskal-Wallis or Friedman tests yielded statistically significant results, post hoc pairwise comparisons were conducted using Dunn's test. The threshold for statistical significance was set at P ≤ 0.05.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Aligner I (0.25 mm/step) | Experimental | Device: Clear aligner, 0.25 mm per stepParticipants received custom removable clear aligners designed to produce 0.25 mm of planar translation per step. Aligners were fabricated from intraoral scans using 0.8 mm Erkodur-AL material. Extrusive and intrusive movements were set at 0.15 mm per step; rotational, tipping, and torquing movements at 1 degree per step. Composite attachments were placed as needed. Participants wore aligners for 22 hours per day and changed to a new aligner every 2 weeks. Interproximal reduction was performed as prescribed. Follow-up visits occurred every 2 weeks. |
| Aligner II (0.35 mm/step) | Experimental | Device: Clear aligner, 0.35 mm per stepParticipants received custom removable clear aligners designed to produce 0.35 mm of planar translation per step. Aligners were fabricated from intraoral scans using 0.8 mm Erkodur-AL material. Extrusive and intrusive movements were set at 0.15 mm per step; rotational, tipping, and torquing movements at 1 degree per step. Composite attachments were placed as needed. Participants wore aligners for 22 hours per day and changed to a new aligner every 2 weeks. Interproximal reduction was performed as prescribed. Follow-up visits occurred every 2 weeks. |
| Control (Fixed Appliance) | Active comparator | Device: Conventional fixed orthodontic applianceParticipants received conventional fixed orthodontic appliances. Stainless steel brackets with a Roth prescription and 0.018-inch slot size, along with bondable molar tubes, were bonded using Transbond XT composite. Leveling and aligning were performed using a standardized progressive sequence of nickel-titanium archwires, advancing to rectangular stainless-steel wires. Archwires were changed every 4 weeks based on clinical response. Participants were seen monthly for checkups. Oral hygiene was reinforced, and appliance complications were addressed. |
Who may qualify
- Ages
- 18 to 40 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (5 listed)
- Age 18 to 40 years
- Non-extraction treatment plan
- Little's Irregularity Index (LII) ≥ 4 mm
- Presence of permanent dentition from first molar to first molar
- Absence of supernumerary teeth or tooth shape anomalies
Key exclusion criteria (5 listed)
- History of prior orthodontic treatment
- Systemic pathologies
- Ongoing use of medications known to influence tooth movement (e.g., prostaglandin inhibitors, bisphosphonates)
- Active periodontal disease
- Belonging to vulnerable populations
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 |
|---|---|---|
| Clear aligner, 0.25 mm per stepAlso: Aligner I, 0.25 mm/step planar translation aligner, 0.25 mm clear alignerParticipants in this group received custom removable clear aligners designed to produce 0.25 mm of planar translation per step. Aligners were fabricated from intraoral scans using 0.8 mm Erkodur-AL material. Extrusive and intrusive movements were set at 0.15 mm per step. Rotational, tipping, and torquing movements were set at 1 degree per step. Composite attachments were placed as needed for tooth movement. Participants wore the aligners for 22 hours per day and changed to a new aligner every 2 weeks. Interproximal reduction was performed as prescribed. | Device | Aligner I (0.25 mm/step) |
| Clear aligner, 0.35 mm per stepAlso: Aligner II, 0.35 mm clear aligner, 0.35 mm/step planar translation alignerParticipants in this group received custom removable clear aligners designed to produce 0.35 mm of planar translation per step. Aligners were fabricated from intraoral scans using 0.8 mm Erkodur-AL material. Extrusive and intrusive movements were set at 0.15 mm per step. Rotational, tipping, and torquing movements were set at 1 degree per step. Composite attachments were placed as needed for tooth movement. Participants wore the aligners for 22 hours per day and changed to a new aligner every 2 weeks. Interproximal reduction was performed as prescribed. | Device | Aligner II (0.35 mm/step) |
| Conventional fixed orthodontic applianceAlso: Fixed appliance, Traditional braces, 0.018-inch Roth bracketsParticipants in this group received conventional fixed orthodontic appliances. Stainless steel brackets with a Roth prescription and 0.018-inch slot size, along with bondable molar tubes, were bonded using Transbond XT composite. Leveling and aligning were performed using a standardized progressive sequence of nickel-titanium archwires, advancing to rectangular stainless-steel wires. Archwires were changed every 4 weeks based on clinical response. Participants were seen monthly for checkups. | Device | Control (Fixed Appliance) |
Primary outcome
Change in Little's Irregularity Index (LII)
Time frame: Baseline; every 2 weeks for the aligner groups and monthly for the control group; up to 20 weeks.
LII is a quantitative score of mandibular anterior crowding. It was measured from intraoral digital scans at baseline and at each follow-up visit using 3Shape 3D Viewer software. A lower LII indicated less crowding.
2 secondary outcomes
Pain intensity
Time frame: Aligner groups: every 2 weeks. Control group: weekly until crowding resolution. Up to 20 weeks.
treatment duration
Time frame: Up to 20 weeks.
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 17 Sep 2026.
- Individual participant dataSharing planned: No
Related trials for Dental Crowding
Not yet recruiting
Bracketless Orthodontic Treatment (3D-BOT) Versus Conventional Fixed Braces for Mild-to-Moderate Lower Front Tooth Crowding in Adults
Mild-to-Moderate Mandibular Anterior Crowding
Recruiting
Evaluating the Efficacy of Micro-Osteoperforations Technique on the Orthodontic Tooth Movement Acceleration in Moderate Mandibular Anterior Crowding Cases Treated With Clear Aligners
Crowding of Anterior Mandibular Teeth
RecruitingObservational study
Exploration of the Utility of Dental-dedicated MRI for Dentistry
Dental Crowding, Dental Occlusion, Traumatic
Enrolling by invitation
Efficiency, Efficacy, Periodontal & Occlusal Outcomes for Aligners Versus Fixed Orthodontic Appliances in Crowded Incisor Treatment
Crowding of Anterior Mandibular Teeth
Not yet recruiting
Effect of Different Adhesive Systems on White Spot Lesions During Fixed Orthodontic Treatment
Malaligned Teeth, Crowding of Teeth
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 Clear aligner, 0.25 mm per step, Clear aligner, 0.35 mm per step and Conventional fixed orthodontic appliance in people with Dental Crowding and Malocclusion, run by Ain Shams University at 1 site in Egypt.
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 5 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 17 Sep 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 Egypt. 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?
Change in Little's Irregularity Index (LII) (time frame: Baseline; every 2 weeks for the aligner groups and monthly for the control group; up to 20 weeks.). 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 17 Sep 2026.