Menu
Enrolling by invitation NCT07239024

Evaluation of Piezocision Versus Injectable Platelet-rich Fibrin During Orthodontic Canine Retraction Orthodontic Canine Retraction: A Comparative Clinical Study

Phase I Interventional Effect of Piezocision and Injectable Platelets Rich Fibrin on Tooth Movement

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Iprf and piezocision.
Who it may be relevant to
Registry conditions: Effect of Piezocision and Injectable Platelets Rich Fibrin on Tooth Movement. Basic parameters: 14 years — 22 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Evaluation of Piezocision Versus Injectable Platelet-rich Fibrin During Orthodontic Canine Retraction: A Comparative Clinical Stud

Overview

Comparison of piezocisin and injectable platelets rich fibrin during canine retraction

Detailed description

Evaluation of piezocision versus injectable platelet-rich fibrin during orthodontic canine retraction: A comparative clinical study

Interventions

  • Procedure Iprf and piezocision
    Injection of iprf and piezocisin

Primary outcome measures

  • Rate of canine retraction [Time frame: 4 months]

Eligibility criteria

Inclusion Criteria:. An age ranges from 14-22 years. 2. Crowding or protrusion that require 1st premolars extraction, followed by symmetrical canine retractions.

3\. All permanent teeth present, 3rd molars aren't considered. 4. Good oral hygiene. 5. No systemic disease and/or medication that could interfere with orthodontic tooth movement. 6. No previous orthodontic treatment. 7. No evidence of craniofacial anomalies, such as cleft lip and palate or previous history of trauma, bruxism, or parafunction. 8. No tooth size, shape, or root abnormalities visible on patient's radiographic records.

\-

Exclusion Criteria:Patients diagnosed to have an indication for non-extraction approach.

2\. Poor oral hygiene or periodontally compromised patient.

  • 3\. Previous orthodontic treatment. 4. Any implanted assistive (e.g., pacemakers, cochlear implants, etc.). 5. Any skeletal dysplasia or craniofacial malformation. 6. Patients with root resorption, impacted canine or dental anomalies. 7. Any systemic diseases or medications that could interfere with orthodontic tooth movement.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Factorial
Masking
Open label
Primary purpose
Basic science

Study locations

Egypt · 1 center
  • AlAzhar university — Cairo

Identifiers

NCT: NCT07239024 · 1250/5544

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗