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The Effects of Different Activation Protocols of Hycon Device and Vibration Stimulation on Canine Teeth Distalization

NCT03968263 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 25

Last updated 2019-10-04

No results posted yet for this study

Summary

This study will be performed with 25 patients who applied to Erciyes University Faculty of Dentistry for treatment and who need 2 first premolar extraction and maximum anchorage for treatment. In order to increase anchorage in the patient who will start the distalization of canine, mini screw (1.5 mm diameter, 7 mm length) will be applied to the right and left maxillary dentition of the patient under local anesthesia. The hycon device, which has a screw-shaped design for the application of force to both the right and left sides of the maxillary dentition of the patients, will be adapted to the bands in the 1st molar teeth. Patients will be randomly divided into 4 groups. Vibration will be applied to the two groups with the Acceledent device.

Group 1 = The hycon device in this group will be used in accordance with the manufacturer's instructions.

Group 2 = The activation period of the hycon device in this group will be modified.

Group 3 = The hycon device in this group will be used in accordance with the manufacturer's instructions. In addition, patients in this group twice a day for 10 minutes with acceledent device vibration will be applied.

Group 4 = The activation period of the hycon device in this group will be modified. In addition, patients in this group twice a day for 10 minutes with acceledent device vibration will be applied.

The period of canine distalization of orthodontic treatment is one of the important stages affecting the duration of treatment. Shortening this time in the clinic will shorten the duration of treatment.

If this application changes the tooth movement speed in any direction, it will support the new research.

Conditions

  • Tooth Migration

Interventions

DEVICE

Hycon device(Routine protocol)

Hycon device will be activated half a turn every 3 days.

DEVICE

Hycon device(Modified protocol)

The activation period of the hycon device will be modified.

DEVICE

Hycon device(Routine protocol) and Vibration(Acceledent)

Hycon device will be activated half a turn every 3 days. Vibration will be applied 2 times 10 minutes per day.

DEVICE

Hycon device(Modified protocol) and Vibration(Acceledent)

The activation period of the hycon device will be modified. Vibration will be applied 2 times 10 minutes per day.

Sponsors & Collaborators

  • TC Erciyes University

    lead OTHER

Principal Investigators

  • Osman Yildiz, Research as. · Research as.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
12 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-02-08
Primary Completion
2020-05-01
Completion
2021-02-08

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03968263 on ClinicalTrials.gov