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Effect of Platelet Rich Fibrin Tooth MovementPhase 1NCT05429437

Assesment of Two Different Modalities of Maxillary Canine Retraction Assisted With Injectable Platelet Rich Fibrin

A Phase 1 study testing Injectable platelet rich fibrin . in people with Effect of Platelet Rich Fibrin Tooth Movement, run by Al-Azhar University at 1 site in Egypt.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The present prospective clinical study will be undertaken for assessment of two different modalities of maxillary canine retraction assisted with injectable platelet rich fibrin. Read more about this study

Who is it for?
Ages 15 to 22 yearsHealthy volunteers can take part
What is being tested?
Injectable platelet rich fibrin .
Type of treatment
Injection or infusion
Could I receive a placebo?
No, everyone receives an active treatment
How many people
18 participants
Where
1 siteEgypt
Study dates
1 Nov 2022to 1 Aug 2023
Phase
Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 15 to 22 years
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult

Who may be able to join

  • An age range 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.

Who cannot join

  • 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.

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • AlAzhar university

    Cairo

Other trials in Egypt

About this study

Official title: Assesment of Two Different Modalities of Maxillary Canine Retraction Assisted With Injectable Platelet Rich Fibrin: A Prospective Clinical Study

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

Being tested
Injectable platelet rich fibrin .

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Injectable platelet rich fibrin .Biological

    i-PRF with maxillary canine retraction that will be performed two times on intervention sides according to a standardized protocol.

  • Injectable platelet rich fibrin .Biological

    i-PRF that will be performed four times on intervention sides according to a standardized protocol.

Study groups in NCT05429437
Study groupRoleWhat they receive
Group IActive comparatorwill include 9 patients
Receives: Biological: Injectable platelet rich fibrin .
Group IIActive comparatorwill include 9 patients.
Receives: Biological: Injectable platelet rich fibrin .

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. assessment of acceleration of canine retraction

    rate of canine retraction

    Measured: post interventional at 4 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted23 Jun 2022
  2. Study start1 Nov 2022 (estimated)
  3. Primary completion1 Mar 2023 (estimated)
  4. Study completion1 Aug 2023 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Factorial
Masking
None (open label)
Enrolment
18 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05429437
Sponsor's protocol ID
785/274
Status last verified
Nov 2022
First submitted
19 Jun 2022
Last updated
14 Nov 2022
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • 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.

    PubMed 33481053
  • Erdur EA, Karakasli K, Oncu E, Ozturk B, Hakki S. Effect of injectable platelet-rich fibrin (i-PRF) on the rate of tooth movement. Angle Orthod. 2021 May 1;91(3):285-292. doi: 10.2319/060320-508.1.

    PubMed 33459765

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing Injectable platelet rich fibrin . in people with Effect of Platelet Rich Fibrin Tooth Movement, run by Al-Azhar University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 14 Nov 2022. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

assessment of acceleration of canine retraction (time frame: post interventional at 4 months). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT05429437, which also lists 2 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Nov 2022.

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