Assessment of Two Different Modalities of Maxillary Canine Retraction Assisted With Micro-osteoperforations Versus Injectable Platelet Rich Fibrin: A Comparative Clinical Study
Trial Snapshot
- Phase
- Phase 2
- Status
- Enrolling By Invitation
- Sponsor
- Al-Azhar University
- Enrollment
- 18
- Locations
- 1
- Primary Endpoint
- 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
Study Overview
Brief Summary
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.
Detailed Description
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 Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Factorial
- Primary Purpose
- Basic Science
- Masking
- None
Eligibility Criteria
- Ages
- 15 Years to 22 Years (Child, Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •An age ranges from 15-22 years.
- •Severe crowding or protrusion requiring 1st premolars extractions followed by symmetrical canine retraction.
- •All permanent teeth present, 3rd molars are excluded.
- •Good oral and general health.
- •No systemic disease/medication that could interfere with OTM.
- •No previous orthodontic treatment.
Exclusion Criteria
- •Patient diagnosed to have an indication for non-extraction approach.
- •Poor oral hygiene or periodontally compromised patient.
- •Patient with craniofacial anomalies or previous history of trauma, bruxism or parafunctions.
- •Previous orthodontic treatment.
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
Time Frame: 4months
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
Secondary Outcomes
No secondary outcomes reported
Investigators
farouk ahmed hussein
Principal Investigator
Al-Azhar University