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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05178771
Other study ID # PRF effect on perio-parameters
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 1, 2022
Est. completion date September 25, 2022

Study information

Verified date September 2022
Source University of Baghdad
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


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.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date September 25, 2022
Est. primary completion date August 5, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 15 Years to 70 Years
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Platelet rich fibrin
Intravenous blood (obtained by venipuncture of the antecubital vein) will be collected in two 10-mL sterile tubes without any anticoagulants and will be immediately centrifuged at 3,000 revolutions (400 × g) per minute for 10 minutes. A structured fibrin clot in the middle of the tube, just between the red corpuscles (RBCs) at the bottom and the acellular plasma at the top, will be separated from the RBCs using sterile tweezers and scissors and transferred on a sterile PRF box. The PRF will be then brought to a thickness of 1 mm by gently compressing in PRF box. Standardized PRF pieces will be obtained by measuring by a periodontal probe and cutting into 3 × 5 mm dimensions. The PRF pieces will be inserted into the periodontal pockets by filling the pockets from the base up to the gingival margin. A modified gingivectomy knife, of which the tip is made blunt, will be used. The PRF volume will be calculated by recording how many pieces will be inserted.

Locations

Country Name City State
Iraq Babylon University Hilla Babel

Sponsors (1)

Lead Sponsor Collaborator
University of Baghdad

Country where clinical trial is conducted

Iraq, 

Outcome

Type Measure Description Time frame Safety issue
Primary clinical parameters measurements of pocket depth in millimeter at baseline and at the end of study 4 weeks and 3 months
Secondary PDGF-BB and periostin level in GCF Measurement of PDGF-BB and periostin level in GCF in baseline data and at the end of study 4 weeks and 3 months
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