NCT06520761

Brief Summary

The purpose of the present study is to compare the effect of injectable platelet fibrin and Low Level LASER therapy on the rate of upper canine retraction, and on root resorption of the canine

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Nov 2022

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

November 1, 2022

Completed
1.7 years until next milestone

First Submitted

Initial submission to the registry

July 20, 2024

Completed
5 days until next milestone

First Posted

Study publicly available on registry

July 25, 2024

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2024

Completed
Last Updated

July 25, 2024

Status Verified

October 1, 2023

Enrollment Period

2.1 years

First QC Date

July 20, 2024

Last Update Submit

July 20, 2024

Conditions

Outcome Measures

Primary Outcomes (1)

  • Rate of canine retraction

    measure the rate of distal movement of the upper canine

    4 month

Secondary Outcomes (1)

  • Root resorption of upper canine

    4 month

Study Arms (2)

injectable platelet rich fibrin

EXPERIMENTAL

blood sample is collected from the patient, centrifuged at 700rpm for 3 minutes then the resulted injectable platelet rich fibrin is injected around the upper right canine while the upper left canine act as a control

Procedure: Injectable platelet rich fibrin

Low Level LASER

EXPERIMENTAL

low level laser from diode laser machine is applied around the upper right canine and the upper left canine acts as a control

Device: Low Level LASER

Interventions

blood sample obtained from the participant, centrifuged at 700 rpm to produce injectable platelet rich fibrin, this will be injected around the upper canine

injectable platelet rich fibrin

Diode LASER device is used to apply Low Level LASER around the upper canine

Low Level LASER

Eligibility Criteria

Age18 Years - 25 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Patients with age 18 years or older.
  • Presence of all permanent teeth except for the third molar.
  • Presence of malocclusion requiring maxillary first premolar extraction such as (class II division 1 or bimaxillary dentoalveolar protrusion).

You may not qualify if:

  • Patient with a history of previous orthodontic treatment.
  • Medical problems may interfere with orthodontic treatment.
  • Bad oral hygiene.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Dental Medicine for Girls Al Azhar university

Cairo, Naser City, 02, Egypt

Location

Related Publications (1)

  • Zeitounlouian TS, Zeno KG, Brad BA, Haddad RA. Effect of injectable platelet-rich fibrin (i-PRF) in accelerating orthodontic tooth movement : A randomized split-mouth-controlled trial. J Orofac Orthop. 2021 Jul;82(4):268-277. doi: 10.1007/s00056-020-00275-x. Epub 2021 Jan 22.

    PMID: 33481053BACKGROUND

Related Links

MeSH Terms

Conditions

Root Resorption

Interventions

Low-Level Light Therapy

Condition Hierarchy (Ancestors)

Tooth ResorptionTooth DiseasesStomatognathic Diseases

Intervention Hierarchy (Ancestors)

Laser TherapyTherapeuticsPhototherapy

Study Officials

  • Samir A Ebrahim, Professor

    Head of orthodontic department at faculty of Dental Medicine for Girls Al-Azhar university

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER GOV
Responsible Party
SPONSOR

Study Record Dates

First Submitted

July 20, 2024

First Posted

July 25, 2024

Study Start

November 1, 2022

Primary Completion

December 1, 2024

Study Completion

December 1, 2024

Last Updated

July 25, 2024

Record last verified: 2023-10

Data Sharing

IPD Sharing
Will not share

Locations