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Using Platelet Rich Fibrin in treating Gingival Recession

Evaluation of Platelet Rich Fibrin in the Management of Gingival Recession Type I/II by Miller

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190614043892N2
Enrollment
22
Registered
2019-09-01
Start date
2017-06-05
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

Gingival Recession. Gingival Recession

Interventions

Intervention 1: Intervention group: gingival recession will be treated by using Platelt rich fibrin (which will be prepared from patient's blood) with coronally advanced flap to cover the graft and th

Sponsors

Damascus University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: Patient age range from 20-45 years old with the ability to demonstrate a good oral hygiene Subjects be periodontally and systemically healthy Subjects presented gingival recessions type I or II of Miller.

Exclusion criteria

Exclusion criteria: Patients who were smokers (more than 20 cigarettes a day) patients suffering from systemic diseases or periodontal diseases patients under orthodontic treatment patients who can’t maintain a good oral hygiene patients who had previous surgical treatments to cover the recession in the chosen area pregnancy or lactating presence of restorative materials in the chosen area

Design outcomes

Primary

MeasureTime frame
Gingival recession depth. Timepoint: Before intervention and 6, 12 months after intervention. Method of measurement: It was recorded by measuring the distance between cemento-enamel junction and gingival margin using calibrated UNC-15 probes (PCP UNC-15, Hu Friedy, Chicago IL).

Secondary

MeasureTime frame
Probing Depth. Timepoint: Before intervention and 6, 12 months after intervention. Method of measurement: The probing depth was recorded using calibrated UNC-15 probes (PCP UNC-15, Hu Friedy, Chicago IL).;Clinical Attachment Level. Timepoint: Before intervention and 6, 12 months after intervention. Method of measurement: It is calculated by adding the probing depth to the gingival recession depth.;Width of Keratinized Gingiva. Timepoint: Before intervention and 6, 12 months after intervention. Method of measurement: It was recorded by measuring the distance between gingival margin and muco-gingival junction using calibrated UNC-15 probes (PCP UNC-15, Hu Friedy, Chicago IL).;Root Coverage. Timepoint: After 6, 12 months of intervention. Method of measurement: Root Coverage (RC, in percentage) was calculated by the following formula:(Gingival recession depth at baseline - gingival recession depth at 6/12 months) ×100 ÷ Gingival recession depth at baseline.;Complete Root Coverage. Timepoint: After 6, 12 months of intervention. Method of measurement: It was recorded by calculating the sites in which complete root coverage was achieved.

Countries

Syrian Arab Republic

Contacts

Public ContactMueataz Al-Qershi

Damascus University

mutazalqrashi@yahoo.com+963 11 211 2623

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026