The Effectiveness of Early Intervention to Correct the Position of PDC:s

Randomized Clinical Trial Clinical Trial

— PDC  

Official title:

The Effectiveness and Cost-effectiveness of Early Intervention to Correct the Position of a Palatally Displaced Maxillary Permanent Canine: A Multicentre RCT

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06267989
• Other study ID #: Gothenburg University
• Status: Recruiting
• Phase: N/A
• Start date: February 12, 2024
• Est. completion date: December 30, 2027

Study information

• Verified date: February 2024
• Source: Region Örebro County
• Contact: Farhan Bazargani, DDS, PhD
• Phone: +46707546107
• Email: farhan.bazargani[@]gu.se
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Approximately 2-3% of children will have problems with one or both of their permanent or 'adult' canine teeth in the upper jaw. These canine teeth sometimes fail to erupt properly, because they are displaced into the roof of the mouth or palate. These are known as palatally displaced canines, PDC, (Brin et al., 1986, Ericson and Kurol, 1987). In addition to failing to erupt, displaced teeth can cause problems, such as damage to the roots or displacement of the neighbouring teeth (Ericson and Kurol, 1988a, Ericson and Kurol, 2000, Falahat et al., 2008).

It has been suggested that if the primary ('baby' or 'milk') canine is extracted at an appropriate time in a child with a suspected palatally displaced canine, then the displaced tooth might spontaneously correct its position (Ericson and Kurol, 1988b) and the extraction of the baby canine when a clinician suspects that the adult canine is displaced has become accepted clinical practice (Short, 2009). This appears to be on the basis of one report of a series of 35 children who received the intervention and no control group (Ericson and Kurol, 1988b). Two recent systematic reviews have examined the evidence for the effectiveness of removal of the primary canine with the aim of correcting the eruption path of a palatally displaced canine. A recent systematic review published in The Cochrane Library in 2021 (Benson et al., 2021) noted that the evidence for any intervention to correct the eruption path of a displaced permanent canine is weak and further research is required. Numerous problems with the reported studies were identified by both reviews.

Other authors have suggested that using a RME (Rapid Maxillary expansion) or headgrear (EOT) to create sufficient space within the dental arch for the permanent canine tooth will encourage the tooth to erupt (Baccetti et al., 2011). This approach might be less traumatic to a child who may have had no experience of dental treatment, other than routine check-ups. If either or both approaches are shown to be effective then their widespread use would be advantageous to both the child and the healthcare provider, because the need for an operation, under general anaesthetic, to uncover the tooth and extensive brace treatment to straighten the tooth will be avoided.

Description:

Design: A multicentre, parallel 3-group, randomised clinical trial. Setting: Orthodontic Departments in Sweden (5 centres), Germany (5 centres) and the UK (Sheffield).

Target Population: Children, aged 10-12 years. Inclusion criteria: One or both upper permanent canine teeth are not palpable or there is a pronounced difference in the eruption between the left and right side. Dental radiographs will be taken to confirm that the permanent tooth is displaced. Canines in sector 5 are going to be excluded from this trial.

Exclusion criteria: Buccal displacement of the canine(s), missing permanent lateral incisors; severe upper arch dental crowding (>2mm in each affected quadrant) or associated pathology.

Intervention: The trial will examine the effectiveness of early orthodontic intervention, either by removal of the baby canine tooth or opening space for the adult tooth, against no treatment.

Primary outcome

• The proportion of young people who do not require surgery after 18 months from randomisation.

Secondary outcomes

• Cost effectiveness of the interventions

• Prevalence and severity of damage to surrounding teeth either due to the unerupted tooth or orthodontic intervention.

Sample size: A sample size calculation suggests that we will need to recruit 300 children (100 per group), assuming a dropout rate of 20%.

Research questions The study aim is to investigate whether early intervention, in children with one or both palatally displaced permanent maxillary canine, prevents the need for later more invasive, prolonged and costly surgical intervention.

Secondary research questions will include:

• What is the cost of early intervention compared with late intervention (surgery to uncover the tooth)?

• Is there a higher or lower incidence of damage to the surrounding teeth following early intervention?

• Are there any adverse effects of early intervention?

The trial efficacy objective will be to evaluate:

• The proportion of participants who have to undergo a surgical operation to uncover or expose the unerupted permanent canine after 18 months from randomisation (primary outcome).

Methods Population Children, aged 10-12 years with at least one palatally displaced maxillary permanent canine.

Interventions Participants will be randomised, using a centralised web-based system, with allocation stratified according to the position of the unerupted canine. The severity of displacement is important when deciding which treatment might be appropriate. Current practice is to extract the baby tooth in children with moderately displaced permanent teeth, but to retain the baby tooth if the permanent tooth is severely displaced. Canine teeth that are severely displaced towards the midline are thought to be less likely to respond to intervention than those nearer to the ideal position (Bazargani et al. 2014, Naoumova et al., 2015).

Young people with moderately displaced permanent canines (Sectors 2, 3 & 4 (Ericson and Kurol, 1988b), Figure below, will be allocated to one of 3 parallel arms:

• Control: no treatment;

• TrtA: open space between the lateral incisor and primary first molar/permanent premolar, to at least 9 mm, to ensure that there is sufficient space into which the canine can erupt; the space is to open whether with fixed appliance in the upper jaw and push coil or with RME

• TrtB: the primary canine(s) removed.

The allocation ratio within the stratum will be: Control: 1; TrtA: 1; TrtB:1. Data from previous studies suggest that in about 14% of young people with a palatally displaced canine the tooth is severely displaced towards the midline (Sectors 4, see ref above (Ericson and Kurol, 1988b)). For young people with a moderately displaced permanent canine there is some evidence that extracting the primary tooth might improve the position of the permanent tooth, hence the design of a three-arm trial. This will generate preliminary evidence of the relative efficacy between the two active arms. Patients with both upper canine teeth affected, but with different degrees of displacement, will be randomised according to the position of the most severely displaced tooth.

Comparator Those in the comparator group will have no treatment during the observation period of 18 months following diagnosis. Any necessary surgical or orthodontic treatment will be provided after this time if the permanent canine shows no signs of appearing in the mouth.

Outcomes The primary outcome will be the proportion of children who do not require surgery after 18 months from randomisation. This will be determined by the clinician treating the participants who will decide if the canine(s) is (are) in such a position that an orthodontic appliance can be placed without the need for surgical intervention. This will also be assessed, by independent judges, from masked clinical photographs taken at T2.

Secondary outcomes will include patient reported outcomes:

• The cost-effectiveness of the interventions

Other secondary outcomes will be:

• Prevalence and severity of damage to surrounding teeth (eg resorption of roots);

• Other adverse events, such as damage to the tooth enamel by orthodontic appliances.

All outcomes are going to evaluated according to the intention-to-treat (ITT) analysis.

Proposed sample size and analyses The total number of patients required depends on the expected prevalence of the three strata. Assuming an effect size of 0.455 [ Nauomova et al., 2015] and further assuming a 20% drop-out, we will allocate 100 subjects to TrtA, 100 to TrtB and 100 to control (total 300), which gives a 90% power.

The primary outcome will be evaluated using a logistic regression with treatment (control vs TrtA or control vs TrtB) and strata as covariates. The same analysis will be used to evaluate the potential damage to surrounding teeth.

The economic analysis will be used to assess any differences in the cost effectiveness of early versus late intervention (surgical exposure). Costs of surgical exposures is going to be adapted from Björksved et al. [Björksved et al.; 2021].

Recruitment rate The recruitment rate per centre would be one participant every two months; therefore, to achieve a sample size of 300 participants in at least 15 centres would require 24 months.

Procedure Children with uni- or bilateral PDC:s meeting the inclusion criteria and their care givers/parents obtain information about the trial, both verbally and in writing. The children and their parents will be allowed at least one week to decide whether they wish to participate in the trial. After informed consent is obtained, the participants are randomly allocated to 1 of 3 groups. A computer-generated randomization is undertaken to ensure that there are equal numbers allocated to each group. Allocation concealment is held by one individual per centre, not involved with the trial.

In the TrtA group, the space creation will be achieved either through bonding fixed appliances in the upper jaw combined with the use of an open-coil or via RME (band on the first upper molars and arms stretching up to the first primary molars/ first premolars). The RME activation protocol is as follows: a single activation (0.25 mm) daily for a period of 14 days, followed by activation every other day until the point at which the palatal cusps of the maxillary first molars contacted the buccal cusps of the mandibular first molars).

Within Sweden, TrtB group is set to receive a space-maintaining appliance, a lingual arch, after the extraction of the primary canines. This is in order to preserve the arch perimeters throughout the observation period.

Study casts (preferably digital casts) at different timepoints (T0 = baseline, T1= 12 mon follow-up and T2 = 18 mon follow-up, see flowchart) are going to facilitate the monitoring of the space relationships in the dental arch.

Standardized panoramic radiographs at T0, T1 and T2 is going to be used to monitor the PDC:s angulation and potential improvement or worsening during the observations period of 18 months.

CBCT (cone beam computed tomography) at T0 and T2 are going to determine the presence or absence of root resorptions at baseline and T2 and the exact location of the PDC at baseline and at the end of the trial.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 318
• Est. completion date: December 30, 2027
• Est. primary completion date: December 30, 2027
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 10 Years to 12 Years

Eligibility

Inclusion Criteria:

• One or both upper permanent canine teeth are not palpable or there is a pronounced difference in the eruption between the left and right side. Dental radiographs will be taken to confirm that the permanent tooth is displaced. Canines in sector 5 are going to be excluded from this trial.

Exclusion Criteria:

• Buccal displacement of the canine(s), missing permanent lateral incisors; severe upper arch dental crowding (>2mm in each affected quadrant) or associated pathology.

Related Conditions & MeSH terms

• Palatal Expansion Technique
• Randomized Clinical Trial

Intervention

Procedure:
• Extraction of the primary canine teeth
Extraction of the primary teeth has show to be successful in some cases.
• Expansion
Expansion of the maxilla with rapid maxillary expander with no extractions

Locations

Country	Name	City	State
Sweden	Gothenbrug University	Gothenburg

Sponsors (1)

Lead Sponsor	Collaborator
Region Örebro County

Country where clinical trial is conducted

Sweden, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Succeful eruption of the palatally displaced canines into the dental arch	The proportion of young people who do not require surgery after 18 months from randomisation.	18 months after intervention
Secondary	Cost effectiveness of the interventions	The proportion of young people who do not require surgery after 18 months from randomisation.	18 months
Secondary	Prevalence and severity of damage to surrounding teeth either due to the unerupted tooth or orthodontic intervention.	Prevalence of root resorptions to the adjacent teeth measured with computed tomography	18 months