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Assesment of rotated teeth relapse after orthodontic treatment via fibrotomy with scalpel and diode laser: A Randomized clinical trail

Assesment of rotated teeth relapse after orthodontic treatment via fibrotomy with scalpel and diode laser: A Randomized clinical trail

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210621051653N1
Enrollment
90
Registered
2021-08-04
Start date
2021-07-28
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

The rate of relapse after orthodontic treatment with fibrotomy.

Interventions

Intervention 1: Intervention group: Fibrotomy with a surgical razor. Intervention 2: Intervention group: Low power laser fibrotomy only (by Biolase EPIC X laser diode USA, wavelength 940 nm). Interven

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 30 Years

Inclusion criteria

Inclusion criteria: Patients undergoing fixed orthodontic treatment who were 15 to 30 years old at the beginning of treatment and had rotated teeth and are now at the end of their fixed treatment should have a rotation rate of 20 to 70 degrees. Absence of systemic disease Absence of gingivitis and periodontitis, good oral hygiene, plaque index below 10% Absence of proximal caries and deep caries in the area of ??cementoenamel junction (CEJ), absence of evolutionary and anatomical deformities Do not take drugs that disrupt bone metabolism Lack of conditions in which the use of lasers is prohibited, such as pregnancy

Exclusion criteria

Exclusion criteria: Teeth with periodontitis Tooth rotations greater than 70 degrees and less than 20 degrees Teeth with proximal caries or caries extending to the cementoenamel junction (CEJ) Taking drugs that affect bone metabolism

Design outcomes

Primary

MeasureTime frame
The rate of relapse after orthodontic treatment with fibrotomy. Timepoint: The beginning of the study, one month after starting treatment. Method of measurement: Digimizer image analysis software.

Secondary

MeasureTime frame
Depth of gingival sulcus. Timepoint: The beginning of the study, one month after treatment. Method of measurement: Using a periodontal probe.;Depth of probing around the teeth. Timepoint: The beginning of the study, one month after treatment. Method of measurement: Using a periodontal probe.;The amount of pain. Timepoint: The beginning of the study, one month after treatment. Method of measurement: VAS scale.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactavideh maboudi

Mazandaran University of Medical Sciences

Avideh48188@yahoo.com+98 11 3326 3345

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 8, 2026