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Oral Health Related Quality of Life and Clinical Outcomes in Patients Undergoing Canine Disimpaction

Oral Health Related Quality of Life and Clinical Outcomes in Patients Undergoing Canine Disimpaction- A Randomized Control Trial.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01917604
Enrollment
40
Registered
2013-08-06
Start date
2022-01-05
Completion date
2025-01-31
Last updated
2023-09-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tooth, Impacted

Keywords

Open versus Closed surgical technique, Palatally impacted maxillary canine, Orthodontic disimpaction, Oral health related Quality of life

Brief summary

To test the null hypothesis that there are no differences in the OHRQOL and clinical outcomes in patients undergoing palatal canine disimpaction using either open or closed surgical method.

Detailed description

The study design will be a unicentric, randomized controlled clinical trial involving 2 parallel groups. The protocol has been approved by local ethics committee of Jamia Millia Islamia and all participants will be provided with an informed consent agreement. The settings will be the orthodontic department of a dental teaching hospital (Faculty of Dentistry, Jamia Millia Islamia). Participants for the trial will be identified from treatment waiting lists and new patient clinics. Proper randomization procedures and reporting include the following steps. 1. Generation of the random allocation sequence, including details of any restrictions. 2. Allocation concealment. 3. Implementation of the random allocation sequence: information on who generated the allocation sequence, who enrolled the participants, and who assigned them to their groups. OPEN SURGICAL EXPOSURE * Surgically uncover the canine tooth followed by bone removal exposing the largest diameter of the ectopic canine crown. The edges need to be substantially trimmed back and dental follicle removed to prevent reclosure of the very thick palatal mucosa. * Surgical excision of the palatal mucosa-standardized using a preformed wire template. * Coe-pack surgical dressing (GC America Inc, Alsip, IL) will be left in place. * The patient will be reviewed 10 days later and the surgical pack removed and the bracket bonded and force application started once the tooth has erupted sufficiently for an orthodontic attachment to be glued onto its surface, orthodontic brace treatment is commenced to bring the tooth into line. CLOSED SURGICAL EXPOSURE • Surgically uncover the canine tooth and Surgical bone removal exposing the largest diameter of the ectopic canine crown. * An multipurpose attachment with ligature wire and e chain will be bonded to the palatal or buccal surface of the ectopic canine crown (whichever was the most accessible). * An orthodontic attachment (button) with ligature wire and bracket with closed coil spring will be bonded to the palatal or buccal surface of the ectopic canine crown (whichever was the most accessible). Outcome Assessment: The following outcomes will be measured before, during and post orthodontic treatment: Primary Outcome Measures: 1. Oral health based Quality of life of patients undergoing canine disimpaction will be accessed by questionnaire pre-treatment and post treatment (one month after debond) -(Annexure 1 - page 1,2) 2. Oral health based Quality of life of patients undergoing canine disimpaction will be accessed by questionnaire 24 hrs and 10 days after surgical caniine exposure (Annexure 1 - page 3,4). 3. Measurement of clinical outcomes 3 months post debond (details mentioned in Annexure 2). 4. Maxillary Canine Aesthetic Index (one month after debond) - Annexure 3

Interventions

PROCEDUREclosed exposure

closed exposure is compared with control

PROCEDUREopen exposure

the open surgical methods of exposing the canine is compared with control

Sponsors

Council of Scientific and Industrial Research, India
CollaboratorOTHER_GOV
Jamia Millia Islamia
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
13 Years to 25 Years
Healthy volunteers
Yes

Inclusion criteria

Patients with palatally ectopic maxillary canines who required surgical exposure and orthodontic alignment * Age 13-25 years Minimal orthodontic problems other than the ectopic canine * Good oral hygiene and motivated to wear fixed appliances for at least 2 years

Exclusion criteria

Compromising medical conditions (patients requiring antibiotic prophylaxis to prevent infective endocarditis) * Periodontal disease (bleeding on probing, pocket probing depths \_3 mm and decreased bone levels as diagnosed from baseline panoramic imaging) * Cases in which the canine is to be brought into the position of the lateral incisor.

Design outcomes

Primary

MeasureTime frameDescription
Oral health based Quality of life (Annexure 1; page 1 and page 2)pre-treatment and 1 month post treatment (average duration of treatment 18 months )to evaluate change in Oral health based Quality of life of patients undergoing canine disimpaction will be accessed by questionnaire and compared for both groups
Post- surgical Oral health based Quality of life (24 hours after surgical exposure) (Annexure 1; page 3)24 hours after surgical exposurePost- surgical Oral health based Quality of life of patients undergoing canine disimpaction will be accessed by questionnaire and compared for both open and closed groups
Post- surgical Oral health based Quality of life (10th day after surgical exposure)(Annexure 1; page 4)10th day after surgical exposurePost- surgical Oral health based Quality of life of patients undergoing canine disimpaction will be accessed by questionnaire and compared for both open and closed groups
Clinical outcomes - periodontal (Annexure 1; page 5)Three month post debondPeriodontal outcomes of disimpacted canines accessed clinically and compared for both open and closed groups; contralateral canine of maxillary arch will be control group.
Maxillary canine aesthetic index (Annexure 1; page 7)one month after debondcomparision to control side with experimental side of both the groups

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026