Class II MalocclusionMACTWinNCT07404696
Comparison of Early Interceptive Orthodontic Appliances (Traditional and Novel) and Later Fixed Appliance Treatment in Class II Malocclusion.
A study testing Head gear activator, Twin Block and Invisalign mandibular advancement in people with Class II Malocclusion and Class II Malocclusion, Division 1, run by Vastra Gotaland Region at 3 sites in Sweden.
Trial summary
Background Approximately 15% of children have a Class II malocclusion, where the maxilla is positioned anterior to the mandible, and around 90% of these children also present with an increased overjet. Read more about this study
- Who is it for?
- Ages 9 to 13 years
- Conditions the study is for
- Class II Malocclusion, Class II Malocclusion, Division 1, Overjet
- What is being tested?
- Head gear activator, Twin Block and Invisalign mandibular advancement
- Type of treatment
- Medical device
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 144 participants
- Where
- 3 sitesSweden
- Study dates
- 15 Jan 2026to 1 Mar 2031
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 9 to 13 years
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Children age 9-13 years at the start of the trial
- Mixed dentition, DS3M1
- Excessive overjet ≥6 mm
- First permanent molars in at least half cusp Cl II relation bilaterally
- Incomplete lip closure
Who cannot join
- Treatment needing extractions due to severe crowding
- Earlier orthodontic treatment
- Mouth breathing
- Ongoing sucking habits
- Syndromic patients
Trial locations and contacts
3 sites in 1 country. Contact the study team or a site near you to ask about taking part.
Sweden3 sites
Sahlgrenska Academy
Gothenburg, 40530
Orthodontic Specialist Clinic
Halmstad, 30246
Orthodontic Specialist Clinic
Kungsbacka, 43441
About this study
Official title: Early Interceptive (Headgear-Activator, Twin Block, Invisalign MA) Versus Later Fixed Appliance Treatment in Class II Malocclusion: A Randomized Clinical Trial
Background Approximately 15% of children have a Class II malocclusion, where the maxilla is positioned anterior to the mandible, and around 90% of these children also present with an increased overjet. Increased overjet is associated with a higher risk of dental trauma and psychosocial consequences such as bullying and reduced oral health-related quality of life (OHRQoL).
Functional orthodontic appliances (e.g., headgear-activator and Twin-block) have long been used to reduce overjet through dentoalveolar effects and by influencing mandibular position and growth. More recently, digital solutions such as Invisalign's mandibular advancement appliance have been introduced, with potential advantages including improved wear time and simultaneous tooth alignment. However, there is currently limited evidence regarding treatment outcomes, patient experience, and cost-effectiveness of these newer appliances compared with established functional appliances.
Read more
Aim The primary aim is to compare treatment outcomes, patient experience, and cost-effectiveness of interceptive orthodontic treatment using three different appliances. The overall aim is to determine whether interceptive treatment of Class II malocclusion with large overjet is effective, and if so, which interceptive modality should be preferred.
Study design and setting
A total of 144 patients aged 9-13 years with Class II malocclusion and large overjet will be randomized into four groups:
- Headgear-activator
- Twin-block
- Aligner Mandibular advancement
- Control
Participants will be treated at four Orthodontic Specialist Clinics within the National Health Service in Region Halland and Västra Götaland, Sweden. Treatments will be provided by two experienced orthodontic specialists.
Follow-up and data collection
Clinical examinations will be performed at:
- Baseline (T0)
- 9 months into treatment (T1)
- End of treatment (T2) Appliance checks will occur every 8 weeks. Digital scans of the occlusion will be collected at T0, T1, and T2. Lateral cephalometric radiographs will be taken at T0 and T2.
Outcomes and planned analyses
The trial will generate three studies with distinct outcomes:
- Treatment outcomes Primary outcome: dental treatment effectiveness measured as overjet reduction. Secondary outcomes: other dental variables, skeletal outcomes, and extraoral outcomes.
- Patient-reported outcomes All treated patients will complete two digital questionnaires:
- Child Perception Questionnaire (CPQ): assesses the child's perception of their teeth before and after treatment.
- Orthodontic Treatment Impact Questionnaire (OTIQ): assesses the child's experience of orthodontic treatment and the appliance. These outcomes will be used to evaluate changes in OHRQoL from pre- to post-treatment and to compare experiences across treatment modalities.
- Cost-effectiveness analysis The economic evaluation will include direct, indirect, and societal costs. Treatment duration, number and length of appointments, and cancellations/no-shows will be recorded.
- Direct costs: premises, staff salaries, materials, and laboratory costs.
- Indirect costs: parental loss of income due to absence from work.
- Societal costs: direct + indirect costs. Costs will be related to treatment outcomes to estimate cost-effectiveness across the treatment arms.
Additional comparison: early vs late treatment Furthermore, after completing 18 months the control group, and half of the functional appliance patients will receive treatment with fixed appliances. This enables an additional comparison of early interceptive treatment versus later treatment using the same outcomes: treatment effectiveness, patient-reported outcomes, and cost-effectiveness.
- Being tested
- Head gear activator, Twin Block, Invisalign mandibular advancement, Fixed appliance
- Medical subject headings
- Overbite, Malocclusion, Angle Class II
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Head gear activatorDevice
Activator with extra orala head gear traction
Twin BlockDevice
Twin Block orthodontic appliance
Invisalign mandibular advancementDevice
Invisalign mandibular advancement featuring occlusal blocks
Fixed applianceDevice
Fixed appliance in upper and lower jaw
| Study group | Role | What they receive |
|---|---|---|
| Head gear activator | Experimental | Treatment with head gear activator orthodontic appliance. Receives: Device: Head gear activator |
| Twin Block | Experimental | Treatment with Twin Block appliance Receives: Device: Twin Block |
| Invisalign Mandibular Advancement | Experimental | Treatment with Invisalign mandibular advancement featuring occlusal blocks. Receives: Device: Invisalign mandibular advancement |
| Fixed appliance | Experimental | Participants will serve as an observation (no treatment) control group during the trial period for 18 months. After completion of the observation phase, they will receive orthodontic treatment with fixed appliances. Outcomes from this delayed intervention will be compared with the three early intervention groups. Receives: Device: Fixed appliance |
What is being measured
The primary outcome is the main question the study is designed to answer.
Part I: Dental treatment result: Overjet reduction
Change in dental overjet compared to baseline. Unit: millimetres (mm). Direction of effect: Lower post-treatment overjet (i.e. greater reduction from baseline) indicates a better outcome; higher overjet values indicate a worse outcome.
Measured: 18 months
Secondary outcomes (1)
Part I: Dental treatment result: Sagittal relation, overbite
Sagittal relationship at the end of treatment, evaluated by both molar and canine relationships. Unit: millimetres (mm).
Direction of effect:
Change towards Class I in molar and canine relation compared with baseline is favorable.
Measured: 18 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Feb 2026
- Study start15 Jan 2026 (estimated)
- Primary completion1 Mar 2031 (estimated)
- Study completion1 Mar 2031 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Class II MalocclusionStudies of the same condition, open and under way.
- More trials run by Vastra Gotaland RegionThe 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
- Model description
- Prospective randomized controlled, investigator-blinded, multicentre clinical trial.
- Masking
- Double blind
- Who is masked
- Investigator, Outcomes assessor
- Enrolment
- 144 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Vastra Gotaland Region
- Sponsor type
- Other government
- Collaborators
- Västra Götalandsregionen, Region Halland, Göteborg University
- Responsible party
- Principal investigator, Anna Westerlund, Göteborg University
- Investigators
- Anna Westerlund, Professor, Principal investigator, Department of Orthodontics, Institution of Odontology, Sahlgrenska Academy, University of Gothenburg
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07404696
- Sponsor's protocol ID
- RCT: Comparing Class II TX
- Acronym
- MACTWin
- Status last verified
- Feb 2026
- First submitted
- 17 Dec 2025
- Last updated
- 11 Feb 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided: Charing individual patient data is not approved in the ethical approval.
Study at a glance
From the registry record, last updated by the sponsor on 11 Feb 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Early Interceptive (Headgear-Activator, Twin Block, Invisalign MA) Versus Later Fixed Appliance Treatment in Class II Malocclusion: A Randomized Clinical Trial
- ClinicalTrials.gov ID
- NCT07404696
- Acronym / sponsor ID
- MACTWin / RCT: Comparing Class II TX
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 144 participants (estimated)
- Lead sponsor
- Vastra Gotaland RegionOther government
- Collaborators
- Västra Götalandsregionen, Region Halland, Göteborg University
- Study start
- 15 Jan 2026 (estimated)
- Primary completion
- 1 Mar 2031 (estimated)
- Study completion
- 1 Mar 2031 (estimated)
- First posted
- 11 Feb 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.
Background Approximately 15% of children have a Class II malocclusion, where the maxilla is positioned anterior to the mandible, and around 90% of these children also present with an increased overjet. Increased overjet is associated with a higher risk of dental trauma and psychosocial consequences such as bullying and reduced oral health-related quality of life (OHRQoL).
Functional orthodontic appliances (e.g., headgear-activator and Twin-block) have long been used to reduce overjet through dentoalveolar effects and by influencing mandibular position and growth. More recently, digital solutions such as Invisalign's mandibular advancement appliance have been introduced, with potential advantages including improved wear time and simultaneous tooth alignment. However, there is currently limited evidence regarding treatment outcomes, patient experience, and cost-effectiveness of these newer appliances compared with established functional appliances.
Aim The primary aim is to compare treatment outcomes, patient experience, and cost-effectiveness of interceptive orthodontic treatment using three different appliances. The overall aim is to determine whether interceptive treatment of Class II malocclusion with large overjet is effective, and if so, which interceptive modality should be preferred.
Study design and setting
A total of 144 patients aged 9-13 years with Class II malocclusion and large overjet will be randomized into four groups:
- Headgear-activator
- Twin-block
- Aligner Mandibular advancement
- Control
Participants will be treated at four Orthodontic Specialist Clinics within the National Health Service in Region Halland and Västra Götaland, Sweden. Treatments will be provided by two experienced orthodontic specialists.
Follow-up and data collection
Clinical examinations will be performed at:
- Baseline (T0)
- 9 months into treatment (T1)
- End of treatment (T2) Appliance checks will occur every 8 weeks. Digital scans of the occlusion will be collected at T0, T1, and T2. Lateral cephalometric radiographs will be taken at T0 and T2.
Outcomes and planned analyses
The trial will generate three studies with distinct outcomes:
- Treatment outcomes Primary outcome: dental treatment effectiveness measured as overjet reduction. Secondary outcomes: other dental variables, skeletal outcomes, and extraoral outcomes.
- Patient-reported outcomes All treated patients will complete two digital questionnaires:
- Child Perception Questionnaire (CPQ): assesses the child's perception of their teeth before and after treatment.
- Orthodontic Treatment Impact Questionnaire (OTIQ): assesses the child's experience of orthodontic treatment and the appliance. These outcomes will be used to evaluate changes in OHRQoL from pre- to post-treatment and to compare experiences across treatment modalities.
- Cost-effectiveness analysis The economic evaluation will include direct, indirect, and societal costs. Treatment duration, number and length of appointments, and cancellations/no-shows will be recorded.
- Direct costs: premises, staff salaries, materials, and laboratory costs.
- Indirect costs: parental loss of income due to absence from work.
- Societal costs: direct + indirect costs. Costs will be related to treatment outcomes to estimate cost-effectiveness across the treatment arms.
Additional comparison: early vs late treatment Furthermore, after completing 18 months the control group, and half of the functional appliance patients will receive treatment with fixed appliances. This enables an additional comparison of early interceptive treatment versus later treatment using the same outcomes: treatment effectiveness, patient-reported outcomes, and cost-effectiveness.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (investigator, outcomes assessor)
- Number of arms
- 4
- Model description
- Prospective randomized controlled, investigator-blinded, multicentre clinical trial.
| Arm | Type | Receives |
|---|---|---|
| Head gear activator | Experimental | Device: Head gear activatorTreatment with head gear activator orthodontic appliance. |
| Twin Block | Experimental | Device: Twin BlockTreatment with Twin Block appliance |
| Invisalign Mandibular Advancement | Experimental | Device: Invisalign mandibular advancementTreatment with Invisalign mandibular advancement featuring occlusal blocks. |
| Fixed appliance | Experimental | Device: Fixed applianceParticipants will serve as an observation (no treatment) control group during the trial period for 18 months. After completion of the observation phase, they will receive orthodontic treatment with fixed appliances. Outcomes from this delayed intervention will be compared with the three early intervention groups. |
Who may qualify
- Ages
- 9 to 13 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (5 listed)
- Children age 9-13 years at the start of the trial
- Mixed dentition, DS3M1
- Excessive overjet ≥6 mm
- First permanent molars in at least half cusp Cl II relation bilaterally
- Incomplete lip closure
Key exclusion criteria (5 listed)
- Treatment needing extractions due to severe crowding
- Earlier orthodontic treatment
- Mouth breathing
- Ongoing sucking habits
- Syndromic patients
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 |
|---|---|---|
| Head gear activatorActivator with extra orala head gear traction | Device | Head gear activator |
| Twin BlockTwin Block orthodontic appliance | Device | Twin Block |
| Invisalign mandibular advancementInvisalign mandibular advancement featuring occlusal blocks | Device | Invisalign Mandibular Advancement |
| Fixed applianceFixed appliance in upper and lower jaw | Device | Fixed appliance |
Primary outcome
Part I: Dental treatment result: Overjet reduction
Time frame: 18 months
Change in dental overjet compared to baseline. Unit: millimetres (mm). Direction of effect: Lower post-treatment overjet (i.e. greater reduction from baseline) indicates a better outcome; higher overjet values indicate a worse outcome.
1 secondary outcome
Part I: Dental treatment result: Sagittal relation, overbite
Time frame: 18 months
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Feb 2026.
- Individual participant dataSharing planned: Undecided. Charing individual patient data is not approved in the ethical approval.
Related trials for Class II Malocclusion
Enrolling by invitation
Discision as Acceleration Method in Canine Retraction in Orthodontics With Aligner and Fixed Appliances in Young Adults a Split Mouth Study
Bimaxillary Protrusion, Class II Div 1 Malocclusion
Recruiting
Maxillary Arch Distalization With Infrazygomatic Crest Miniscrews for Class II Malocclusion
Class II Malocclusion
Recruiting
Comparing 3D-Printed and Milled Titanium Plates in Jaw Surgery (Le Fort I): Accuracy and Operative Time
Malocclusion, Angle Class II, Malocclusion, Angle Class III
Recruiting
Treatment of Mild Class II Malocclusion in Adult Patients With Clear Aligners Versus Fixed Multibracket Therapy
Malocclusion, Class II Malocclusion
Recruiting
Patient-Reported Outcomes for Different Orthodontic Thermoplastics Used in Clear Aligners
Malocclusion of Anterior Teeth, Malocclusion in Children
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.
Anna Westerlund, Professor principal investigator
Department of Orthodontics, Institution of Odontology, Sahlgrenska Academy, University of Gothenburg
3 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Head gear activator, Twin Block and Invisalign mandibular advancement in people with Class II Malocclusion and Class II Malocclusion, Division 1, run by Vastra Gotaland Region at 3 sites in Sweden.
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: opening soon, as of the sponsor's last update on 11 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 3 sites in Sweden. 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Sara Waldenström, PhD student (+46768522129, sara.waldenstrom@regionhalland.se), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Part I: Dental treatment result: Overjet reduction (time frame: 18 months). 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 11 Feb 2026.