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Treatment Of Shallow Periodontal Pockets Using PRF As an Adjunct To Scaling And Root Planing In Periodontitis Patients

U

University of Baghdad

Status

Not yet enrolling

Conditions

Periodontitis

Treatments

Other: PRF

Study type

Interventional

Funder types

Other

Identifiers

NCT05890157
PRF as adjunct to ScRp

Details and patient eligibility

About

Platelet rich fibrin (PRF) has been widely used in regenerative dentistry since it provides plenty amount of growth factors that enhance wound healing and tissue regeneration. Platelet derived growth factor-BB (PDGF-BB) is a growth factor with essential functions such as regulation of cell migration, proliferation, and differentiation. This study aims to evaluate the efficacy of PRF in improving the clinical periodontal parameters and GCF level of PDGF-BB.

Full description

Split mouth randomized clinical trial is the design of the study. 12 periodontitis patients with 24 opposite shallow periodontal pockets (4-6 mm in depth) will be selected. Randomization in this study will be achieved using toss of coin method in which periodontal pockets will be designated either control site or test site. PRF will be used as an adjunct to scaling and root planing to treat the test sites. While control sites were treated by scaling and root planing only. Clinal periodontal parameters were recorded and GCF level of PDGF-BB will be measured at baseline and1- and 3- month follow-up visits to evaluate the healing response to the treatment.

Enrollment

12 estimated patients

Sex

All

Ages

20 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

•periodontitis

Exclusion criteria

  • Periodontal therapy for the last 3 months
  • Medical history of systemic diseases such as diabetes.
  • Patients wearing dental prosthesis
  • Alcoholic patients
  • Teeth with grade II mobility, endodontic lesions, and teeth with untreated caries

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

12 participants in 2 patient groups

Test ScRp+PRF
Experimental group
Description:
This site will treated by ScRp+PRF
Treatment:
Other: PRF
Control ScRp
No Intervention group
Description:
This site will treated by ScRp only

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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