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Effect of Micro-osteo-perforations on the Rate of Alignment of Mandibular Anterior Teeth.

Effect of Micro-osteo-perforations on the Rate of Alignment of Mandibular Anterior Teeth.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05132764
Enrollment
30
Registered
2021-11-24
Start date
2021-01-01
Completion date
2022-06-30
Last updated
2021-11-24

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

Conditions

Orthodontics

Keywords

Microosteoperforations, Little's index, Rate of tooth movement

Brief summary

Micro osteoperforation is an easy, safe and effective method of accelerating orthodontic tooth movement by 2-3 times.it has been reported to increased the osteoblastic activity and some acceleration of the rate of canine retraction,reducing the treatment duration and associated side effects. The aim of this study is to assess the effect of MOPs on the rate of alignment of mandibular anterior teeth.

Detailed description

MATERIAL AND METHODS: STUDY DESIGN: Two parallel arm randomized controlled clinical trial SETTING: Orthodontics Department, Rehman College of Dentistry. DURATION OF STUDY: one year SAMPLING TECHNIQUE: non-probability consecutive sampling. SAMPLE SELECTION: INCLUSION CRITERIA 1. Malocclusion cases with mandibular anterior segment crowding. 2. Age range 13-30 years. EXCLUSION CRITERIA: 1. Missing lower anterior tooth. 2. Systemic diseases/Medications affecting bone biology. 3. Previous orthodontic treatment. 4. Poor oral hygiene status. 5. Active periodontal disease 6. Syndromes. DATA COLLECTION Written informed consent from the patients will be taken after clarification of the purpose of the intervention and the associated risks and benefits. Orthodontic treatment will be started in all subjects using fixed preadusted edgewise appliance (0.022-in MBT prescription, Ortho Organizers, Inc. USA). After bonding of lower arch the patients will be randomized into control and experimental groups. Patients will be randomly allocated, through computer generated tables in Microsoft Excel Software, into parallel groups with a 1:1 allocation ratio. Allocation will be concealed in opaque envelopes and opened only at the time of intervention. Local anesthesia will be given in lower arch on each side approximately 1cm from labial frenum. Two points for screw insertion will be demarcated on buccal mucosa, in each interdental segment, by bleeding points using a calibrated periodontal probe. Probe tip will be inserted to the level of bone to measure the thickness of gingiva. The measurement will be added to the depth of perforation needed i-e 2 - 3 mm into the bone. First point will be marked at a distance of 3mm from free gingival margin and second point will be marked 3mm from the first one. Orthodontic miniscrew (AbsoAnchor, Korea) of 1.3 mm diameter will be used for MOPs to the depth of 2-3 mm into the buccal cortical bone. An endodontic rubber stopper will be set for required / optimal depth on miniscrew and MOPs will be performed. After the intervention, the patients will be instructed for maintaining good oral hygiene and to take analgesics, such as acetaminophen, only if necessary. The control group will receive no MOPs at the alignment stage. Alignment will be started in both control and experimental groups using 0.012 NiTi (North American Braces, USA). Both the groups will be followed every month for maximum six months. Digital scan of lower arch will be taken on each visit. Each scan will be labelled for identification, date of scan taking and little index score .For reliability 20 randomly selected scan will be rescored for little index by the same examiner as well as another examiner after 2 weeks for intra and inter-examiner reliability.

Interventions

2 inter radicular bone microosteoperforations using temporary anchorage device tip.

Sponsors

Rehman Medical Institute - RMI
Lead SponsorOTHER

Study design

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

Masking description

The assessor and the investigator will have no knowledge of the intervention in the digital models.

Intervention model description

Two parallel arm randomized controlled clinical trial

Eligibility

Sex/Gender
ALL
Age
13 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

1. Malocclusion cases with mandibular anterior segment crowding. 2. Age range 13-30 years.

Exclusion criteria

1. Missing lower anterior tooth. 2. Systemic diseases/Medications affecting bone biology. 3. Previous orthodontic treatment. 4. Poor oral hygiene status. 5. Active periodontal disease 6. Syndromes

Design outcomes

Primary

MeasureTime frameDescription
Rate of alignment of lower anterior teeth6 monthsRate of alignment of lower anterior teeth

Secondary

MeasureTime frameDescription
clinical crown length6 mothsclinical crown length

Countries

Pakistan

Contacts

Primary ContactShahida Jehan, BDS
shahida.jehan@rmi.edu.pk03438901267
Backup ContactSohrab Shaheed, FCPS
sohrab.shaheed@rmi.edu.pk03339327608

Outcome results

None listed

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