Maxillary Canine Retraction Assisted With Micro-osteoperforations Versus Injectable Platelet Rich Fibrin

Al-Azhar University18 enrolled

Overview

The present clinical comparative study will be undertaken for assessment of two different modalities of maxillary canine retraction assisted with microosteoperforations versus injectable platelet rich fibrin.

Group I: will include 9 patients who willreceive MOPs with maxillary canine retraction that will be performed on intervention sides according to a standardized protocol. ▪ Group II: will include 9 patients receive i-PRF that will be performed on intervention sides according to a standardized protocol.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

BASIC_SCIENCE

Masking

NONE

Enrollment

Conditions

Effects of; Movement of Teeth Assiste Wit MOPS and I-prf

Interventions

injectable platelet rich fibrin versus microosteoperforationCOMBINATION_PRODUCT

injectable platelet rich fibrin which is second product of blood versus microosteoperforation which is surgical procedure

Eligibility

Sex: ALLMin age: 15 YearsMax age: 22 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: 1. An age ranges from 15-22 years. 2. Severe crowding or protrusion requiring 1st premolars extractions followed by symmetrical canine retraction. 3. All permanent teeth present, 3rd molars are excluded. 4. Good oral and general health. 5. No systemic disease/medication that could interfere with OTM. 6. No previous orthodontic treatment. Exclusion Criteria: 1. Patient diagnosed to have an indication for non-extraction approach. 2. Poor oral hygiene or periodontally compromised patient. 3. Patient with craniofacial anomalies or previous history of trauma, bruxism or parafunctions. 4. Previous orthodontic treatment.

Locations (1)

AlAzhar university

Cairo, Egypt

Outcomes

Primary Outcomes

Direct clinical assessment of the amount of maxillary canine retraction i.e. amount of extraction space closure before and after four months observation period and on every 28 days observation period according to standardized method

Direct clinical assessment of the amount of maxillary canine retraction i.e. amount of extraction space closure before and after four months observation and every 28 days period and on every 28 days observation period according to standardized method. 2. Study cast assessment: • The amount of maxillary canine retraction on both sides will be measured immediately before starting canine retraction and at each observation interval by using a software for the scanned models according to standardized method

Time frame: 4months

Data from ClinicalTrials.gov

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