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Micro-osteoperforations on the Rate of Canine Retraction

Effect of Micro-osteoperforations on the Rate of Canine Retraction; A Split-mouth Randomized Controlled Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04968327
Enrollment
10
Registered
2021-07-20
Start date
2017-01-01
Completion date
2017-08-30
Last updated
2021-07-20

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

Conditions

Malocclusion

Brief summary

the study aimed to clinically evaluate the effect of micro-osteoperforations on the rate of tooth movement, as evaluated by its effect on the rate of canine retraction.

Detailed description

Ten adult patients requiring maxillary first premolars' extraction were enrolled in this split-mouth randomized controlled clinical trial. Micro-osteoperforations were randomly assigned to one side of the maxillary arch at the canine-premolar region, and the contralateral side served as the control. Mini-screws were used for anchorage reinforcement, and canine retraction was performed using nickel-titanium closed coil springs, delivering a force of 150 grams per side. The primary outcome was the measurement of canine retraction rate throughout the study period from digital dental models obtained every 3 weeks. The secondary outcome was the detection of possible canine tipping during retraction.

Interventions

MOPs included shallow perforations of the buccal cortical plate surrounding the tooth that requires orthodontic tooth movement, with no flap reflection was performed using a surgical bur using the special calibrated device called PROPEL

using nickel-titanium (NiTi) closed coil-springs delivering a force of 150 grams per side

Sponsors

Hams Hamed Abdelrahman
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Intervention model description

split-mouth

Eligibility

Sex/Gender
ALL
Age
15 Years to 20 Years
Healthy volunteers
No

Inclusion criteria

* healthy systemic condition with no chronic diseases * no previous orthodontic treatment * adequate oral hygiene * have a healthy periodontium * signed an informed consent

Exclusion criteria

* have a chronic disease * previous orthodontic treatment * poor oral hygiene or periodontal conidition

Design outcomes

Primary

MeasureTime frameDescription
Rate of canine retraction12 weeksmeasurements were recorded from digital dental models every 3 weeks

Secondary

MeasureTime frameDescription
Measurment of canine tipping12 weeksTipping of the maxillary canine during retraction was also evaluated from digital dental models

Countries

Egypt

Outcome results

None listed

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