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Investigating the effect of intra-oral LED device and low level laser therapy on the rate of orthodontic maxillary canine movement compared with control group: a randomized clinical trial

Investigating the effect of intra-oral LED device and low level laser therapy on the rate of orthodontic maxillary canine movement compared with control group: a randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20120220009086N4
Enrollment
60
Registered
2019-06-01
Start date
2019-06-10
Completion date
Unknown
Last updated
2019-08-26

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

Conditions

Anomalies of tooth position of fully erupted teeth. Anomalies of tooth position of fully erupted tooth or teeth

Interventions

Intervention 1: Intervention group1: Laser therapy is performed using the China Gigaa laser machine (dental diode laser Gigaa). The laser used is Ga Al As laser with a wavelength of 810 nm and a power

Sponsors

Hamedan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 25 Years

Inclusion criteria

Inclusion criteria: orthodontic treatment plan that needs extraction of maxillary first premolar unilaterally or bilaterally presence of maxillary canine, second premolar and first molar at the side of extraction of first premolar

Exclusion criteria

Exclusion criteria: canine root dilaceration long-term consuming nonsteroidal anti inflammatory drugs a and hormonal supplements parafunctional habits crossbite in canine area poor periodontal health pregnancy and lactating history of previous fixed orthodontic treatment

Design outcomes

Primary

MeasureTime frame
Rate of tooth movement. Timepoint: at start of study, 1,2 and 3 months after intervention. Method of measurement: 3D scanner and software.;Pain. Timepoint: two weeks after intervention. Method of measurement: modified McGill questionair.;Rotation of the canine. Timepoint: at start of study, 1,2 and 3 months after intervention. Method of measurement: 3D scanner and software.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMozhde Borjali

Hamedan University of Medical Sciences

mozhde.borjali@yahoo.com+98 81 3838 1059

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 21, 2026