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The Effect of Multiple Injections of (PRF) on The Rate of Canine Retraction

Cairo University (CU) logo

Cairo University (CU)

Status and phase

Enrolling
Phase 3

Conditions

Platelet-Rich Fibrin
Orthodontics
Acceleration

Treatments

Procedure: Injectable platelet rich fibrin (i-PRF): in acceleration of orthodontic tooth movement

Study type

Interventional

Funder types

Other

Identifiers

NCT05766618
I-PRF in orthodontics

Details and patient eligibility

About

this clinical trial aims to prove that multiple injections will produce a steady rate of acceleration of orthodontic tooth movement.

Full description

Platelet-rich fibrin injection is a second-generation platelet concentrate, prepared from centrifuged blood which is a rich source of platelets, stem cells, and growth factors seven times greater than that released by platelet-rich plasma. It is a simplified procedure with no biochemical manipulation of blood, free from anticoagulants which are known to inhibit wound healing or any gelling agent, and easily usable with a low rate of mistakes during the preparation procedure.

A variety of growth factors are released by PRF such as platelet-derived growth factor (PDGF), transforming growth factor β (TGF-β), and vascular endothelial growth factor (VEGF), which play a crucial role in angiogenesis, collagen synthesis, and bone regeneration.

Treatment with extraction especially in adult patients may take a longer time due to reported increase in bone density and lower bone regenerative rate. Also, the retraction process to close extraction spaces most of the time is accompanied by bone loss and root resorption as reported in the previous studies. i-PRF can accelerate tooth movement, in addition, prevent tooth retraction undesirable side effects.

Enrollment

22 estimated patients

Sex

All

Ages

16 to 24 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • adult patient
  • Full set of permanent dentition (excluding third molars).
  • Good oral hygiene
  • protrusion cases that require extraction of premolars (Bimaxillary protrusion or class II div 1)

Exclusion criteria

  • History of previous orthodontic treatment.
  • Systemic disease or drugs affecting tooth movement.
  • Smokers
  • Poor oral health that precludes orthodontic treatment (presence of caries, active white spots, or periodontal diseases)
  • Severe crowding cases with ectopic erupted canines

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

22 participants in 2 patient groups

injection site
Experimental group
Description:
it is the arm where the patients will receive the PRF injection intraligamentally in distobuccal, and distopalatal areas of the distal surface of the canine also submucosal injection will be given buccally and palatially (0.25mm) for each side in either the right or left side of the arch.
Treatment:
Procedure: Injectable platelet rich fibrin (i-PRF): in acceleration of orthodontic tooth movement
control site
No Intervention group
Description:
it is the arm where the patients will not receive any injection with the same method of retraction as the intervention side.

Trial contacts and locations

1

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Central trial contact

Mohamed M Alkhawaga, BDS

Data sourced from clinicaltrials.gov

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