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Variation in Rate of Orthodontic Tooth Movement in Response to Platelet Rich Plasma Therapy

Variation in Rate of Orthodontic Tooth Movement in Response to Platelet Rich Plasma Therapy

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04016727
Enrollment
10
Registered
2019-07-11
Start date
2018-07-02
Completion date
2020-02-02
Last updated
2020-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tooth Movement

Keywords

tooth movement, platelet rich plasma

Brief summary

PRP from 5 ml blood was prepared and 60 units were injected into the buccal vestibule of patient before initiating canine retraction using NiTi coil spring. Pre and post cervical, incisal and mid distances were measured using Vernier calliper.

Detailed description

Platelet rich plasma was prepared using patients own blood. The production of PRP began with a 6-mL homologous blood sample that was withdrawn from the donor via venupuncture. One milliliter of the blood sample was set apart to determine the concentration of platelets and leukocytes in whole blood. The remaining 5 mL was mixed with an anticoagulant (3.8%, 1-mL sodium citrate) to prevent clotting. The blood sample was centrifuged at 113 g for 5 minutes to separate the plasma containing the platelets from the red cells. The plasma was drawn off the top and centrifuged for an additional 2 minutes at 3772 g to separate the platelets. Suitable platelet concentrations were achieved by the resuspension of PRP with plasma (high platelet concentration, 5 times the concentration in whole blood).

Interventions

BIOLOGICALplatelet rich plasma

Platelet rich plasma was prepared using patients own blood. 60 units of PRP was injected on one side of the arch using insulin syringe. Each patient served as his/her own control (the side with PRP injected) and experimental group (the side without PRP injected). Whether the right or left side served as control or experimental was determined by lottery method. Patients were recalled after 4 weeks and the measurements were repeated again between lateral incisors and canines at mid, cervical and incisal of the teeth and their mean was recorded.

Sponsors

Armed Forces Institute of Dentistry, Pakistan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
11 Years to 20 Years
Healthy volunteers
Yes

Inclusion criteria

* patients requiring first premolar extractions

Exclusion criteria

* patients taking any drugs, steroids, NSAIDs and antibiotics * patients with any co morbid conditions

Design outcomes

Primary

MeasureTime frameDescription
canine movement in mili meters1 monthdistance was measured using vernier caliper at mid cervical and incisal region

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026