Overview

This trial is active, not recruiting.

Condition malocclusion, angle class ii, division 1
Treatments ffrd and mini plates group, conventional ffrd
Sponsor Sherif A. Elkordy
Start date January 2015
End date August 2016
Trial size 50 participants
Trial identifier NCT02475785, CU001

Summary

The purpose of this study is to determine if the Forsus Fatigue resistant Device appliance with direct skeletal mini plates anchorage is capable of achievement of skeletal mandibular effects while preventing the excessive proclination of the lower incisors at the end of the treatment when compared to the conventional Forsus Fatigue resistant Device appliance applied to the upper and lower dental arches in female patients with skeletal Class II malocclusion

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation randomized
Endpoint classification safety/efficacy study
Intervention model parallel assignment
Masking single blind (outcomes assessor)
Primary purpose treatment
Arm
(Experimental)
Upper will be bonded, levelled and aligned until reaching 0.019 x 0.025 ss archwires. 2 Y shaped mini plates will be inserted in the mandibular symphysis Insertion of the FFRD with Direct application over the mandibular mini plates
ffrd and mini plates group Mini plates anchored FFRD
FFRD direct loading over mini plates inserted in the mandibular symphysis
(Active Comparator)
Upper and lower arches will be bonded, levelled and aligned until reaching 0.019 x 0.025 ss archwires. Insertion of FFRD with application over the lower archwire
conventional ffrd Dental anchored FFRD
FFRD inserted between maxillary and mandibular arches with the pushrods placed distal to mandibular canines
(No Intervention)
Patients will be observed for an average duration of 6-8 months

Primary Outcomes

Measure
correction of the skeletal Class II profile
time frame: expected average of 10 months

Secondary Outcomes

Measure
Dento-alveolar side effects
time frame: expected average of 10 months
Angle of soft tissue convexity
time frame: expected average of 10 months
Position of lips and Chin
time frame: expected average of 10 months

Eligibility Criteria

Female participants from 10 years up to 13 years old.

Inclusion Criteria: - Skeletal Angle Class II division 1 malocclusion with a deficient mandible. (SNB ≤ 76°) - Horizontal or neutral growth pattern. (MMP ≤ 30°) - Increased overjet (min 5 mm) with Class II canine relationship. (minimum of half unit) - Mandibular arch crowding less than 3 mm. - At the time of insertion of the FFRD, the patients had to be in the "Middle Phalanx of the Middle finger" stage G or H (MP3 G or MP3 H stage) according to Rajagopal. Exclusion Criteria: - Systemic Disease. - Any signs or symptoms or previous history of temporomandibular disorders (TMD) as clicking, crepitus, pain, limitation or deviation. - Extracted or missing upper permanent tooth/teeth (except for third molars). - Facial Asymmetry. - Para-functional habits. - Severe proclination or crowding that requires extractions in the lower arch.

Additional Information

Official title Evaluation of Mini Plates Anchorage in Conjunction With Forsus Fatigue Resistant Device for Correction of Skeletal Class II Malocclusion in Growing Subjects: A Randomized Controlled Trial
Principal investigator Sherif Elkordy, Phd
Description 1. Background: Class II malocclusions are characterized by an incorrect relationship between the maxillary and mandibular arches due to skeletal or dental problems or a combination of both. The prevalence of this malocclusion was recently found to be 20.6% in the Egyptian population in the age between 11 and 14 years with mandibular retrusion as its most common characteristic. It was also mentioned that other populations showed the predominance of the mandibular retrusion (80%) as opposed to only 20% expressing excessive maxillary development. Class II profiles attractiveness was previously investigated in the literature. It was found that patients, their peers, orthodontists and oral surgeons, rated subjects with Class I profiles as more attractive than others with Class II profiles. It was also reported that the profile of normal adolescent patients were more favorably perceived by laypersons than untreated Class II division 1 malocclusion subjects. In growing patients having Class II mandibular retrusion, functional orthopedic appliances are commonly used for mandibular advancement based on the concept of growth modification. However, two main problems appeared to compromise the desired treatment outcomes of these appliances; the need for patient cooperation and the lack of the possibility of combining their use with fixed appliance therapy in order to shorten treatment duration. Many systematic reviews and meta-analyses were recently performed in the literature answering the question of whether removable functional appliances (RFAs) produced skeletal effects for correction the skeletal discrepancy through inducing actual increase in mandibular dimensions. Most recently two systematic reviews concluded that the skeletal effects of RFAs were minimal and could be considered of negligible clinical importance. They mentioned that treatment of Class II malocclusion with RFAs was associated with a minimal stimulation of mandibular growth, a minimal restriction of maxillary growth and more significant dento-alveolar and soft tissue changes. Fixed functional appliances were first introduced by Emil Herbst in 1905. Many types of fixed functional appliances were developed since then; including Jasper jumper and Twin force Bite corrector . The Forsus Fatigue Resistant Device (FFRD) was introduced by Bill Vogt in 2006. It represented a semi-rigid fixed functional alternative that was intended to overcome breakage problems of flexible fixed functional appliances. However, it was proven that dental changes were more significant than skeletal changes in the final occlusal results. These changes included mesial movement of the mandibular molars and proclination of the mandibular incisors. These unwanted tooth movements appeared to compromise the actual skeletal correction and jeopardize the stability of the results. Several attempts were proposed to counteract the unwanted dento-alveolar side effects of fixed functional appliances. Use of lingual arches, increase the dimensions of the archwires, the introduction of negative torque in the archwires and the use of lower incisor brackets with lingual crown torque are some examples. Some studies used the mini implants in an attempt to limit the unwanted dental effects of fixed functional appliances. These studies proved that mini implants anchorage reduced the lower incisors proclination but they in turn increased the upper incisors retroclination and were not able to achieve significant skeletal mandibular effects. Titanium mini plates were introduced for the use for orthodontic anchorage in 1999 as a skeletal anchorage system for open bite correction. They were proven to be well accepted by patients and providers, safe and effective adjunct for complex orthodontic cases. Other uses of mini plates in orthodontics included maxillary and mandibular molars distalization and orthodontic anchorage where it was reported that they were able to provide absolute anchorage. Bone anchored maxillary protraction using mini plates was reported to be successful in producing significant forward maxillary growth in Class III growing subjects. Recently mini plates were used for the direct loading of FFRD for correction of skeletal Class II malocclusion. They reported actual skeletal changes through the increase in the mandibular length with minimal dento-alveolar side effects. However, these results are only preliminary and have to be taken with caution because the study did not include control group. 2. Research Hypothesis: The null hypothesis (H0) of this research is that use of direct mini plate anchorage in conjunction with FFRD will not be able to induce skeletal rather than dental effects for correction of the skeletal Class II malocclusion in comparison with conventional FFRD therapy or with untreated growing Class II control subjects. 3. Objectives: The primary objective of this study is to determine if mini plates use in conjunction with FFRD will induce supplemental growth of the mandible in Class II malocclusion subjects with mandibular retrognathism. Secondary objectives include To determine if mini plates use in conjunction with FFRD will be able to: - Reduce the dento-alveolar side effects produced by fixed functional appliances in treatment of skeletal Class II subjects - Correct the soft tissue convexity in Class II subjects - Correct molar and canines relationships - Develop a patients' well-accepted treatment modality for correction of skeletal Class II malocclusion. 4. Study design According to the norms of the CONSORT STATEMENT, this study will be clinical with intervention, in which the allocation of the subjects will be randomized (block randomization). This study will be parallel with blinding for the outcome assessors. The primary purpose of this study will be treatment. 5. Participants - Settings and locations where the data are collected The treatment will be performed in the outpatient clinics of Department of Orthodontics of Cairo State University. This public university predominantly serves low-income population living in Cairo, Egypt. Data will be collected from April 2015 through August 2016. 6. Interventions Two groups will receive treatment. Group 1 will be treated with the FFRD and mini plates anchorage for 10 months or until the correction of the malocclusion . Group 2 will be treated with conventional FFRD for 10 months or until the correction of the malocclusion. A third untreated control group will be included with an observation period of 6-8 months. 7a. Sample size Our sample size calculation is based on a study which compared the use of Herbst appliance with and without mini implants anchorage and reported a significant increase in the Herbst mini screw group over their control group. The mean change in the mandibular length in the treatment and control groups were 4.6±2.43 mm and 0.9±2.09 mm respectively. Thus the mean difference was 3.7 with the within group standard deviation set at 2.26. Because three groups will be compared, Bonferroni adjustment was used as alpha level/number of comparisons = 0.05/3= 0.0167 to adjust for multiple comparisons. Power and Sample size calculation (PS) software (department of biostatistics Vanderbilt University) was used for sample size calculation. A t test was performed with the power was set as 0.9, allocation ratio of 1:1:1 and the Type I error probability (alpha) associated with this test was set as 0.0167. Results of the test showed that "The Group sample sizes of 11, 11 and 11 achieve 90% power to reject the null hypothesis of equal means with a significance level (alpha) of 0.0167" Therefore, 33 subjects will be needed, with 12 subjects in each group. To account for patient loss to follow up (attrition), a sample size of 45 patients will be selected and divided into three groups, fifteen each. 7b. Interim analysis and stopping guidelines In the group with mini plates anchorage, in case of mobility in the mini-plates in any subject, the load will be removed for about two weeks. After that, the load will be restored. If the mobility persists, surgical exposure of the mini plate will be done and either insertion of longer mini screws ion the same mini plate or a change in the position of the mini plate will be done. Any harms, adverse effects or unintended effects of the study intervention will be documented and reported. Post-surgical swelling and pain are anticipated and will be addressed by antibiotics and pain killers. Other unanticipated surgical harms have to be immediately managed and will be reported. Harms related to the orthodontic appliances will be managed by the principal investigator. 8. Randomization 8a. Sequence generation The randomization of the recruited subjects will be done with a randomized list, using random.org website. This list is made by an individual not involved in the clinical trial (S.B.) 8b. Type The type of randomization will be block randomization. The number of blocks and block sized were be blinded to the investigators. 9. Allocation and concealment mechanism - Each patient will be allocated a number from sequentially numbered opaque sealed envelopes after fulfillment of the inclusion criteria and signing the informed consent to be enrolled in the study. - According to the number, the patients will be then allocated into one of the groups using a randomization table. 10. Implementation Before the beginning of the research, the allocation sequence will be generated by a person not involved in the study (Dr S.B.). The random list will be sealed from the principal investigator who will enroll participants. After the participant takes a sealed number, S.B. will be contacted to implement the allocation. All the study contributors will have no access to the random list. The envelopes will be closed with the type of treatment selected for storage of the information. 11. Blinding Blinding will be carried out only for the data assessment because the researchers, participants and subjects can not be blinded. Therefore, a person who does not know the nature of the trial will analyze the data.
Trial information was received from ClinicalTrials.gov and was last updated in January 2016.
Information provided to ClinicalTrials.gov by Cairo University.