Mode
Text Size
Log in / Sign up
N/A N=28 Randomized Single-blind Treatment

Use of Platelet Rich Fibrin in Addition to CAF and SCTG for Treatment of Gingival Recession

Gingival Recession

Enrolled (actual)
28
Serious AEs
0.0%
Results posted
Mar 2021
Primary outcome: Primary: Recession Depth — 2; 2; 0; 0 length in millimeters

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
CAF +SCTG (Procedure); platelet rich fibrin (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Cairo University
Primary completion
Dec 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Recession Depth
2; 2; 0; 0; 0; 0
SECONDARY
Recession Width
1.5; 2; 0; 0; 0; 0
SECONDARY
Root Coverage Gain
92.9; 91.6
SECONDARY
Probing Depth
1.71; 1.5; 1.07; 1.07; 1.07; 1.21
SECONDARY
Clinical Attachment Level
3.79; 4; 2.14; 2.29; 2; 2.07
SECONDARY
Gingival Biotype
1; 1; 3; 2.5; 3; 3
SECONDARY
Width of Keratinized Gingiva
2.36; 2.64; 3.64; 3.71; 3.86; 4.14
SECONDARY
Patient Satisfaction
71.4; 64.3
SECONDARY
Root Coverage Esthetic Score (RES)
9.43; 9.29
SECONDARY
Post Operative Pain
9; 8.5

Summary

This research will be conducted in an attempt to achieve complete root coverage with physiologic probing depth and a harmonious view with the adjacent tissues using Platelet rich fibrin in conjunction with Coronally advanced flap and subepithelial connective tissue graft.

Eligibility Criteria

Inclusion Criteria

  • 1) Patients 18 years and older 2) Buccal recession defects classified as either Miller class I or II gingival recession.
  • Clinical indication and/or patient request for recession coverage 4) Good oral hygiene

Exclusion Criteria

  • 1) Miller Class III and IV gingival recession. 2) Any systemic diseases or any medication. 3) Pregnancy. 4) Patients undergoing radiotherapy. 5) Handicapped and mentally retarded patients. 6) Current and former smokers as smoking is a contra-indication for plastic periodontal surgery .
  • Teeth with cervical restorations, abrasion
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03199118). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search