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

A

Armed Forces Institute of Dentistry, Pakistan

Status and phase

Unknown
Phase 4

Conditions

Tooth Movement

Treatments

Biological: platelet rich plasma

Study type

Interventional

Funder types

Other

Identifiers

NCT04016727
platelet rich plasma

Details and patient eligibility

About

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.

Full 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 The production of PRP began with a 6-mL homologous blood sample that was withdrawn from the donor via venupuncture.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).

Enrollment

10 patients

Sex

All

Ages

11 to 20 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • patients requiring first premolar extractions

Exclusion criteria

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

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

10 participants in 2 patient groups

PRP group
Experimental group
Description:
patients in which 60 units of prp was injected
Treatment:
Biological: platelet rich plasma
Control group
No Intervention group
Description:
patients not given any intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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