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Platelet Rich Fibrin on Root Coverage of Gingival Recessions

Clinical Evaluation of Coronal Advanced Flap and Platelet Rich Fibrin on Root Coverage of Gingival Recessions Over a Period of 24 Month.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04248049
Enrollment
15
Registered
2020-01-30
Start date
2018-01-01
Completion date
2019-11-30
Last updated
2020-01-30

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

Conditions

Gingival Recession

Keywords

platelet-rich fibrin, platelet concentrates, periodontal diseases

Brief summary

Several surgical techniques and various adjunctive agents have been used to covered Gingival Recession (GR) and promote clinical outcomes. The treatment of the GR more used (gold standard) is the root coverage with surgical procedures and connective tissue graft, but it has limitations due to the conditions of the donor graft. Is necessary develop other biomaterials for these cases. The platelet rich fibrin is a autologous biomaterial that has gained tremendous momentum having been utilized for a variety of dental and medical procedures including periodontal surgeries. However, results remain contradictory and mainly focus on the hard and soft tissue healing, aesthetics and postoperative discomfort. The objective of this study was to evaluate the clinical effects of coronal advanced flap (CAF) and CAF + Platelet Rich Fibrin (PRF) on Root coverage (RC) over a period of 24 month.

Interventions

OTHERPlatelet rich fibrin

The roots of patients with diagnosis of gingival recessions will be covered with coronally advanced flap (CAF) and platelet rich fibrin (PRF) (CAF+PRF)

Sponsors

Universidad Antonio Nariño
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Split mouth design allowing to evaluate two conditions in the same patients

Intervention model description

Randomized clinical trial (RCT) (Interventional)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Participant is willing and able to give informed consent for participation in the study * Healthy males and females of age 18-60 years old * Multiple bilateral (maxillary or mandibular) gingival recessions (Miller class І or II) * Good oral hygiene (O´Leary index ≤ 15%)

Exclusion criteria

* Active periodontal disease * Periodontal surgeries in the last three years * Pregnancy or lactation * Smokers or alcoholics * Platelet dysfunction syndrome or thrombocytopenia * Coagulation defects * Uncontrolled diabetes * Medical contraindications to elective oral surgery procedures * Severe immunodeficiencies * Oncological history * Prosthetic restorations adjacent to gingival recessions * Mobility II or III * Occlusal contacts excessive * Root caries * Buccal restaurations Class V

Design outcomes

Primary

MeasureTime frameDescription
Change of percentage of root coverage (PRC) from baseline at 12 and 24 monthsbaseline, 1, 3 , 6, 9, 12 and 24 monthsComplete root coverage after surgical correction measured in percentage by using periodontal probe. PRC= Preoperative recession depth - Postoperative recession depth X 100 % Preoperative recession depth

Secondary

MeasureTime frameDescription
Horizontal gingival recession (HGR)baseline, 1, 3 , 6, 9, 12 and 24 monthsMeasured horizontally between two borders of the recession. (measured using a periodontal probe in millimeters).
Probing depth (PD)baseline, 1, 3 , 6, 9, 12 and 24 monthsIt is measuring the distance from the gingival margin to the base of the pocket using periodontal probe. The probe will be inserted parallel to the long axis of the tooth using light force. (measured using a periodontal probe in millimeters).
Clinical attachment level(CAL)baseline, 1, 3 , 6, 9, 12 and 24 monthsTwo measurements will be used to calculate the CAL: the probing depth and the distance from the gingival margin to the CEJ.
Gingival tissue thicknessbaseline, 1, 3 , 6, 9, 12 and 24 monthsThe gingiva mid-buccally in the attached gingiva will be penetrated with an endodontic reamer with a silicon disc stop. The measure of penetration will be measured with dentimeter (mm).
Vertical gingival recession (VGR)baseline, 1, 3 , 6, 9, 12 and 24 monthsIt is measuring the distance from the cemento-enamel junction (CEJ) to the margin of the gingiva at the midbuccal point of the teeth (measured using a periodontal probe in millimeters).
Gingival bleeding index (IS)baseline, 1, 3 , 6, 9, 12 and 24 monthsEvaluation of the presence and absence of bleeding in the gingival margin through the gingival sulcus. The index is calculated after penetration of the sulcus by the periodontal probe, bleeding surfaces are noted and then counted. The index is calculated by dividing the number of surfaces that bleed by the total number of teeth and then multiplying by 100 to reach the percentage of bleeding index.
Visual analog scale (VAS)baseline, 1, 3 , 6, 9, 12 and 24 monthsVisual analog scale
Evaluation of oral health impact on quality of life, using the Oral Health Impact Profile (OHIP-14) questionnaire.baseline, 1, 3 , 6, 9, 12 and 24 monthsEvaluate the impact of oral health on patient's quality of life before and 1 year after implant installation. This evaluation will be carried out through the application of a questionnaire with 14 questions (Oral Health Impact Profile: OHIP-14) that assess the patient's perception regarding the impact of oral conditions on their well-being
Keratinized tissue height (KTH)baseline, 1, 3 , 6, 9, 12 and 24 monthsTo measure the tissue thickness, a guiding device will be made to standardize the region to be measured and then, at a specific point, the mucosa will be punctured with an endodontic spacer and the thickness marked with a rubber marker. Then, using a digital caliper, the thickness will be measured.

Countries

Colombia

Outcome results

None listed

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