The Effect of Surgical Technique on PDC

Sponsor
University of Oslo (Other)
Overall Status
Recruiting
CT.gov ID
NCT05067712
Collaborator
Jonkoping County Hospital (Other)
80
2
2
84.2
40
0.5

Study Details

Study Description

Brief Summary

Permanent maxillary canines are the second teeth that most commonly assume ectopic positions after the third molars. They are diagnosed as impacted and have an incidence of 1 % to 3%

In their ectopic path of eruption, they can cause damage (resorption) of the adjacent roots, a severe complication that may lead to the loss of anterior teeth. When cone-beam computed tomography (CT) scanning is used for diagnose, root resorption is detected in two-thirds of the lateral incisors adjacent to impacted maxillary canines before treatment.

The treatment of this condition comprises two stages: a surgical intervention to uncover the canine crown followed by orthodontic treatment to move the canine into correct position. The surgical intervention commonly involves two different techniques: the open and the closed technique.

The open technique procedure involves removing the bone and mucosa covering the crown of the canine. The exposed crown is left uncovered and a pack is placed over the area to avoid overgrowth of tissue. When enough spontaneous eruption of the canine has occurred, an orthodontic attachment is bonded to the crown and the tooth is moved above the mucosa with orthodontic appliances into the correct position.

The closed technique procedure involves bonding an orthodontic attachment to the crown with a chain after exposing the canine during the surgery. The palatal flap is sutured back covering the exposed crown and the chain is left through the palatal mucosa free in the oral cavity. Shortly after, the canine is forced to erupt through the palatal mucosa and moved into the correct position with orthodontic appliances.

The purpose of this prospective randomized clinical trial is to compare outcome variables between the Open and Closed surgical exposure techniques regarding the success of treatment, patient's perceptions of pain and discomfort experienced and analgesic consumption, treatment time, and complications. The null hypothesis is that similar outcomes occur when the surgical exposure of palatally impacted canines is performed by using the open or the closed surgical technique.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Open Surgical Exposure Technique
  • Procedure: Closed Surgical Exposure Technique
N/A

Detailed Description

Consecutive patients planned for surgical exposure of uni- or bilateral palatally impacted canines of two centers, are invited to participate in the Trial. The centers are the University Orthodontic Departments of Oslo, Norway, and Jonkoping, Sweden.

Potential participant patients and their parents are given verbal and written information about the Trial and Informed Consent is obtained.

Participants are randomly allocated to one of two interventions by use of Permuted Block Randomization in order to maintain equal allocations across treatment groups. Allocation concealment is held by one individual in each center that is not involved in the study. No stratification is made for age or gender in the two groups.

If the maxillary deciduous canine is present at the time of the surgery, the tooth is removed together with the exposure of the impacted canine.

Before entering the surgery room, participants answer a first questionnaire on whether they are experiencing pain or discomfort (measured in VAS-scales) in the area of the impacted canine and whether they have taken analgesics. The questionnaire is filled in and delivered back before entering the surgery room. After the surgical exposure, verbal and written information and recommendations on chlorhexidine mouth rinse and analgesic consumption are given. A second questionnaire is then handed out for participants to self-report the pain-discomfort they experienced during surgery, and are experiencing in the evening the same day and the following seven days together with the analgesic consumption. The second questionnaire is delivered back to the clinic at the post-surgical control.

At the post-surgical control, participants receive a third questionnaire where they self-report the pain-discomfort they experienced during and after sutures (closed technique) and packing (open technique) are removed.

After the surgical exposure with the open technique, the canine is left to erupt spontaneously. Participants are follow-up by the orthodontist until the canine has erupted enough (approximately ½ - 1/3 of the crown above the level of the palatal mucosa) to bond an attachment to the crown. The canine then starts to be moved into alignment in the dental arch above the mucosa with orthodontic appliances.

After the surgical exposure with the closed technique, the impacted canine starts to be moved with orthodontic appliances within 2 weeks after surgery. The canine is moved into alignment in the dental arch through the mucosa.

From the completion of the surgical exposure phase until the previously impacted canine is orthodontically positioned in the dental arch, similar questionnaires are handed out to the participants in both treatment groups every second/ third orthodontic control.

The participants are followed until the active orthodontic treatment is finished and orthodontic retainers bonded.

Schedule/ registrations:

Before the surgical exposure phase of treatment (T0)

  • Clinical anamnesis

  • Routine dental clinical examination. Assessment of periodontal pocket depth, gingival bleeding on probing, gingival recession in the lateral incisor in the impacted and nonimpacted contralateral side.

  • Study models. Assessment of occlusion traits, presence of maxillary deciduous canine.

  • Panoramic radiograph. Assessment of the position of the impacted canine: mesial position, mesial inclination, and distance to the occlusal line according to Ericson and Kurol.

  • Cephalogram. Assessment of upper incisor sagittal inclination.

  • CBCT (cone beam computed tomography). Assessment of the exact impacted canine position, size of the impacted canine's follicle, crestal bone height in the lateral incisor in the impacted and nonimpacted contra lateral side, root resorption of the impacted canine, lateral incisor, and first premolar in the impacted and nonimpacted contra lateral side

Surgical exposure day (T1)

  • Questionnaires are handed out to the participants for assessment of pain and discomfort (measured on VAS-scale) and analgesic consumption : (1) before surgery same day (2) after surgery same day and following 7 days, (3) post-surgery control same day and following 7 days.

  • Registrations at the surgery: duration of the operation, complications, depth of the impacted canine from the mucosa surface.

The previously palatally impacted canine has erupted (approximately 1/3-1/2 canine crown above palatal mucosa) (T2)

  • Questionnaires are handed out to participants between T1 and T2 for assessment of pain and discomfort (measured on VAS-scale) and analgesic consumption the same day and following 7 days after every second/ third orthodontic control

  • Timespan T1-T2

  • Complications associated with the eruption of the canine since surgery

The previously palatally impacted canine is aligned in the dental arch and ligated to a 0.016 X 0.022 nickel-titanium / standard steel archwire in the 0.018- appliance system or a 0.019 X 0.025 nickel-titanium / standard steed archwire in the 0.022- appliance system (T3)

  • CBCT (cone beam computed tomography). Assessment of the position of the canine root, crestal bone height in the canine, lateral incisor, and first premolar in the impacted and nonimpacted contra lateral side, root resorption of the impacted canine, incisors, and first premolar in the impacted and nonimpacted contra lateral side

  • Questionnaires are handed out to participants between T2 and T3 for assessment of pain and discomfort (measured on VAS-scale) and analgesic consumption the same day and following 7 days after every second/ third orthodontic control

  • Timespan T2-T3

  • Complications associated with the orthodontic alignment of the previously impacted canine into the dental arch.

The active orthodontic treatment is finished and an orthodontic retainer is fitted (T4)

  • Routine clinical examination. Assessment of periodontal pocket depth, gingival bleeding on probing, gingival recession in the canine, incisors and first premolar in the impacted and nonimpacted contra lateral side.

  • Study models. Assessment of occlusion traits.

  • Panoramic radiograph. Assessment of root parallelism, root resorption.

  • Cephalogram. Assessment of upper incisor sagittal inclination.

Except for the CBCT examinations and questionnaires, all the examinations and treatments performed in this trial are the routine examinations and treatments of palatally impacted maxillary canines performed in Norway and Sweeden. All the surgical exposures and orthodontic treatments are performed by or under the supervision of the same specialist in oral surgery and orthodontics, respectively, in each center, with many years of experience.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Treatment of Palatally Displaced Maxillary Canines - a Controlled Randomized Clinical Trial
Actual Study Start Date :
Nov 25, 2017
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Dec 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Open Surgical Exposure Technique

After randomization, the PDC allocated to this arm is surgically exposed with the Open Technique followed by the Orthodontic Treatment phase

Procedure: Open Surgical Exposure Technique
A mucoperiosteal palatal flap is elevated off the bone from the premolar to the midline The bone covering the crown aspect of the canine is removed until the largest diameter of the crown is exposed Follicular tissue is removed from the exposed crown area The flap is repositioned back and sutured The area over the exposed canine crown is excised leaving a window with the crown uncovered. If the tooth is deeply embedded in the bone, a dressing is placed over the uncovered crown and kept in place with sutures. The extraction of the primary canine (if present) is made before or in connection with the surgical exposure. Ten to fifteen days later the dressing and sutures are removed and the tooth is left to erupt autonomously. When the canine has spontaneously erupted above the palatal mucosa an attachment is bonded to the crown and the canine is moved into alignment in the dental arch above the mucosa with orthodontic appliances.

Active Comparator: Closed Surgical Exposure Technique

After randomization, the PDC allocated to this arm is surgically exposure with the Closed technique followed by the Orthodontic Treatment phase.

Procedure: Closed Surgical Exposure Technique
A mucoperiosteal palatal flap is elevated off the bone from the premolar to the midline The bone covering the crown aspect of the canine is removed until the largest diameter of the crown is exposed. Follicular tissue is removed from the exposed crown area. An attachment with a chain is bonded to the exposed canine crown. The flap is repositioned back and sutured to cover the exposed crown leaving the chain through the palatal mucosa free in the oral cavity The extraction of the primary canine (if present) made before or in connection with the surgical exposure Ten to fifteen days later the sutures are removed. Within days, traction is applied to the canine with orthodontic appliances by means of the chain, and the canine is pulled through the palatal mucosa out to the oral cavity and into alignment in the dental arch.

Outcome Measures

Primary Outcome Measures

  1. Success of treatment [Within 3 years from surgery]

    The canine is aligned in the dental arch. "Aligned in the dental arch" meaning the canine being ligated to a 0.016 X .0.22 nickel- titanium/ standard steel in a 0.018-appliance system or to a 0.019 X 0.025 nickel-titanium/ standard steel arch-wire in a 0.022- appliance system

  2. Patient's perceptions of pain-discomfort experience and analgesic consumption [Within 3 years from surgery]

    Perceptions of pain-discomfort experienced and analgesic consumption are self reported on a 100 mm visual analogue scale (VAS) and questionnaires in the first evening and the following 7 evenings, after surgery, after suture and pack removal and after every second/ third orthodontic activation.

Secondary Outcome Measures

  1. Canine eruption time [Within 1,5 years from surgery]

    Time span from the surgery until 1/3 to 1/2 of the canine crown is above the level of the palatal mucosa

Other Outcome Measures

  1. Surgery operation time [1,5 hours]

    Time span (hours, minutes) from the first incision to the last suture

  2. Complications associated with the surgical technique [Within 1,5 years from the surgery]

    Presence, number and type of complications associated with the surgery

  3. Duration of orthodontic treatment [Within 3 years from the surgery]

    Time span from surgery until the canine being ligated to a 0.016 X 0.022 nickel-titanium/

Eligibility Criteria

Criteria

Ages Eligible for Study:
9 Years to 19 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Consecutive patients diagnosed with palatally impacted canine with a sagittal position in Zone 2-4 as documented on panoramic radiographs according to the criteria proposed by Ericson and Kurol,1988, planned to start treatment with surgical exposure of the impacted canine.

  • Patients with uni- or bilateral impacted canines are included. In bilateral impaction cases, the more severely positioned impacted canine according to the Zone (Zone 2 - 4) is included in the trial.

  • No restriction of presenting malocclusion

  • Dental developmental stage: Maxillary DS2M1 and DS3M2 according to Bjork.

  • Age not older than 16 years at surgery

Exclusion Criteria:
  • Agenesis of lateral incisors on the impaction side

  • Peg-shaped lateral incisors on the impaction side

  • Previous orthodontic treatment

  • Subjects with craniofacial deformity/ syndromes

  • Documented learning disability

  • Communication problems related to the language when an interpreter is needed

  • Sagittal position of the impacted canine in Zone 5, according to Ericson and Kurol, documented on panoramic radiographs.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Det Odontologiske Fakultet, avdelingen for kjeveortopedi Oslo Norway 0455
2 Odontologiska Institutionen, avdelingen för ortodonti Jönköping Sweden 551 11

Sponsors and Collaborators

  • University of Oslo
  • Jonkoping County Hospital

Investigators

  • Principal Investigator: Lucete Fe Færøvig, University of Oslo

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Lucete Fernandes faerovig, Principal investigator, University of Oslo
ClinicalTrials.gov Identifier:
NCT05067712
Other Study ID Numbers:
  • 2015715
First Posted:
Oct 5, 2021
Last Update Posted:
Oct 5, 2021
Last Verified:
Sep 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 5, 2021