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Efficacy of PRF Application on Clinical Parameters and GCF Platelet-derived Growth Factor-BB and Periostin Levels

U

University of Baghdad

Status

Completed

Conditions

Periodontitis

Treatments

Other: Platelet rich fibrin

Study type

Interventional

Funder types

Other

Identifiers

NCT05178771
PRF effect on perio-parameters

Details and patient eligibility

About

Determine the efficacy of the non-invasive application of PRF on periodontal clinical parameters(pocket reduction) and the levels of PDGF-BB and Periostin in the gingival crevicular fluid.

Full description

The adjunctive use of PRF with conventional ScRp may improve clinical healing, decrease tissue morbidities such as pain and discomfort, increase patient acceptance, reduce treatment time. Since PRF can be utilized as a safe, natural method to repair tissues at a low cost. Our aim is to evaluate the effectiveness of the non-invasive application of PRF as an adjunct to ScRp in patients with stage III grade B periodontitis through measurements of gingival crevicular fluid levels of PDGF-BB and Periostin before and after treatment and compare it with ScRp alone. A split-mouth procedure will be performed to reduce confounders as possible.

Enrollment

14 patients

Sex

All

Ages

15 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Systemically healthy patients.
  • Patients with periodontitis.

Exclusion criteria

  1. Medical history of systemic disease: diabetes, pregnancy, or lactation.
  2. Previous periodontal treatment for the last 6 months
  3. Grade II mobility
  4. Smoker or alcoholic patient.
  5. Teeth with untreated caries, endodontic lesions
  6. Symptoms of recent acute illness e.g., COVID-19 will be excluded as well

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

14 participants in 2 patient groups

test site
Experimental group
Description:
The test site will receive ScRp in addition to PRF
Treatment:
Other: Platelet rich fibrin
control sites
No Intervention group
Description:
The control site will be treated by ScRp only

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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