The Effect of Combination of Micro-osteoperforation and a Vibration Device on Orthodontic Tooth Movement

The Effect of Combination of Micro-osteoperforation and a Vibration Device on Orthodontic Tooth Movement : A Prospective Randomized Clinical trial

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190108042293N1

Enrollment

Registered

2021-07-31

Start date

2021-07-31

Completion date

Unknown

Last updated

2021-08-30

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

Conditions

Orthodontic Treatment.

Interventions

Intervention 1: The intervention group: receives micro-osteoperforations on both sides (right and left) of the maxilla along with using a C-shaped vibration device (Vpro5, Propel Orthodontics). Interv

Eligibility

Sex/Gender

All

Age

18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Age range : 18 to 45 years Maxillary canine teeth fully erupted Need to extract both first maxillary premolars Existence of 3 mm space after initial alignment Good oral hygiene

Exclusion criteria

Exclusion criteria: Systemic diseases affecting bone metabolism Take any medication Periodontal disease Smoking Pregnancy

Design outcomes

Primary

Measure	Time frame
Rate of orthodontic tooth movement. Timepoint: At the beginning of the study, immediately before canine retraction, and 28 days after the onset of canine retraction. Method of measurement: Digital caliper with an accuracy of 0.01 millimeter and dental casts.	—

Secondary

Measure	Time frame
The level of pain caused by micro-osteoperforation. Timepoint: The day of appliance placement , the day of canine retraction, and subsequently at 24 hours, 7 days, and 28 days after canine retraction. Method of measurement: Numerical rating scale.;The level of patient's drooling caused by micro-osteoperforation and the use of a vibration device. Timepoint: The day of appliance placement , the day of canine retraction, and subsequently at 24 hours, 7 days, and 28 days after canine retraction. Method of measurement: Numerical rating scale.	—

Measure

Time frame

The level of pain caused by micro-osteoperforation. Timepoint: The day of appliance placement , the day of canine retraction, and subsequently at 24 hours, 7 days, and 28 days after canine retraction. Method of measurement: Numerical rating scale.;The level of patient's drooling caused by micro-osteoperforation and the use of a vibration device. Timepoint: The day of appliance placement , the day of canine retraction, and subsequently at 24 hours, 7 days, and 28 days after canine retraction. Method of measurement: Numerical rating scale.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactSarvin Sarmadi

Tehran University of Medical Sciences

sarmadis@sina.tums.ac.ir+98 21 8801 5801

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026