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

Primary Purpose

Gingival Recession

Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
CAF +SCTG
platelet rich fibrin
Sponsored by
Cairo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Gingival Recession focused on measuring root coverage

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

- 1) Patients 18 years and older 2) Buccal recession defects classified as either Miller class I or II gingival recession.

3) 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 .

7) Teeth with cervical restorations, abrasion

Sites / Locations

  • Faculty of dentistry

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

CAF+SCTG+PRF

CAF+SCTG

Arm Description

The patients suffering from class I or II gingival recession in the intervention group will receive a subepithelial connective tissue graft (SCTG) covered by platelet rich fibrin membrane (PRF) followed by a coronally advanced flap (CAF)

Control group patients with class I or II gingival recession will receive treatment that consists of CAF+SCTG only

Outcomes

Primary Outcome Measures

Recession Depth
measured from the cemento-enamel junction to the margin of the gingiva at the mid-buccal point of the teeth at basline, 3 months and 6 months. It is recorded in millimeters (mm) with lower values mean better outcome.

Secondary Outcome Measures

Recession Width
It was measured as the distance from mesial and distal papillae along the CEJ. It is recorded in millimeters (mm) where lower values means a better outcome.
Root Coverage Gain
(preoperative vertical recession - postoperative vertical recession/preoperative vertical recession) x 100.
Probing Depth
measured from the gingival margin to the base of the pocket probe at the midbuccal point of the teeth. Its is recorded in millimeters (mm) where lower values mean better outcome.
Clinical Attachment Level
measured from the CEJ to the base of the sulcus at the midbuccal point of the teeth. Its is recorded in millimeters (mm).
Gingival Biotype
under local anesthesia from 3 mm below the gingival margin trans-gingivally piercing tissues horizontally, perpendicular to the long axis of the tooth until it contacts bone. Its is recorded in millimeters (mm) where higher values mean better outcome.
Width of Keratinized Gingiva
from the margin of the gingiva to the mucogingival junction at the midbuccal point of the teeth. Its is reported in millimeters where higher values mean better outcome.
Patient Satisfaction
printed yes/ no questionnaire with 3 questions: would you do this surgery again? would you recommend this treatment to others? are you satisfied with the results?
Root Coverage Esthetic Score (RES)
The RES system evaluates 5 variables 6 months after surgery: Zero, 3, or 6 points are used for the evaluation of the position of the gingival margin (GM). A score of 0 or 1 point is used for each of the following variables: marginal tissue contour (MTC), soft tissue texture (STT), mucogingival junction (MGJ) alignment, and gingival color (GC). the points are then summed up to obtain one figure representing the RES. minimum value:0 maximum value: 10 which means better outcome for RES
Post Operative Pain
Numerical Rating Scale (NRS) with numbers from 0 to 10 ('no pain' to 'worstpain imaginable') for the first 2 weeks postoperatively

Full Information

First Posted
June 21, 2017
Last Updated
February 22, 2021
Sponsor
Cairo University
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1. Study Identification

Unique Protocol Identification Number
NCT03199118
Brief Title
Use of Platelet Rich Fibrin in Addition to CAF and SCTG for Treatment of Gingival Recession
Official Title
The Use of Coronally Advanced Flap and Subepithelial Connective Tissue Graft With or Without Platelet Rich Fibrin in the Treatment of Miller Class I or II Gingival Recession: a Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
January 1, 2018 (Actual)
Primary Completion Date
December 31, 2019 (Actual)
Study Completion Date
December 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief 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.
Detailed Description
The study population will be divided into 2 groups: Group 1: Patients suffering from Miller class I or II gingival recession will be treated with a coronally advanced flap in conjunction with a sub-epithelial connective tissue graft. The patients should be non-smoker, medically free and above 18 years Group 2: Patients suffering from Miller class I or II gingival recession will be treated with a coronally advanced flap in conjunction with a sub-epithelial connective tissue graft and platelet rich fibrin. the patients should meet the same inclusion criteria mentionned above.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gingival Recession
Keywords
root coverage

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
28 (Actual)

8. Arms, Groups, and Interventions

Arm Title
CAF+SCTG+PRF
Arm Type
Experimental
Arm Description
The patients suffering from class I or II gingival recession in the intervention group will receive a subepithelial connective tissue graft (SCTG) covered by platelet rich fibrin membrane (PRF) followed by a coronally advanced flap (CAF)
Arm Title
CAF+SCTG
Arm Type
Active Comparator
Arm Description
Control group patients with class I or II gingival recession will receive treatment that consists of CAF+SCTG only
Intervention Type
Procedure
Intervention Name(s)
CAF +SCTG
Other Intervention Name(s)
CTG
Intervention Description
the use of coronally advanced flap (CAF) with sub-epithelial connective tissue graft (SCTG) from the palate to cover gingival recession
Intervention Type
Other
Intervention Name(s)
platelet rich fibrin
Other Intervention Name(s)
PRF
Intervention Description
in addition to coronally advanced flap and sub-epithelial connective tissue graft, PRF is also used in the surgical procedure to cover gingival recession
Primary Outcome Measure Information:
Title
Recession Depth
Description
measured from the cemento-enamel junction to the margin of the gingiva at the mid-buccal point of the teeth at basline, 3 months and 6 months. It is recorded in millimeters (mm) with lower values mean better outcome.
Time Frame
baseline-3 months-6 months
Secondary Outcome Measure Information:
Title
Recession Width
Description
It was measured as the distance from mesial and distal papillae along the CEJ. It is recorded in millimeters (mm) where lower values means a better outcome.
Time Frame
baseline-3 months-6 months
Title
Root Coverage Gain
Description
(preoperative vertical recession - postoperative vertical recession/preoperative vertical recession) x 100.
Time Frame
at 6 months
Title
Probing Depth
Description
measured from the gingival margin to the base of the pocket probe at the midbuccal point of the teeth. Its is recorded in millimeters (mm) where lower values mean better outcome.
Time Frame
baseline-3 months-6 months
Title
Clinical Attachment Level
Description
measured from the CEJ to the base of the sulcus at the midbuccal point of the teeth. Its is recorded in millimeters (mm).
Time Frame
baseline-3 months-6 months
Title
Gingival Biotype
Description
under local anesthesia from 3 mm below the gingival margin trans-gingivally piercing tissues horizontally, perpendicular to the long axis of the tooth until it contacts bone. Its is recorded in millimeters (mm) where higher values mean better outcome.
Time Frame
baseline-3 months-6 months
Title
Width of Keratinized Gingiva
Description
from the margin of the gingiva to the mucogingival junction at the midbuccal point of the teeth. Its is reported in millimeters where higher values mean better outcome.
Time Frame
baseline-3 months-6 months
Title
Patient Satisfaction
Description
printed yes/ no questionnaire with 3 questions: would you do this surgery again? would you recommend this treatment to others? are you satisfied with the results?
Time Frame
questionnaire given to the patient 6 months after the surgery
Title
Root Coverage Esthetic Score (RES)
Description
The RES system evaluates 5 variables 6 months after surgery: Zero, 3, or 6 points are used for the evaluation of the position of the gingival margin (GM). A score of 0 or 1 point is used for each of the following variables: marginal tissue contour (MTC), soft tissue texture (STT), mucogingival junction (MGJ) alignment, and gingival color (GC). the points are then summed up to obtain one figure representing the RES. minimum value:0 maximum value: 10 which means better outcome for RES
Time Frame
6 months
Title
Post Operative Pain
Description
Numerical Rating Scale (NRS) with numbers from 0 to 10 ('no pain' to 'worstpain imaginable') for the first 2 weeks postoperatively
Time Frame
after 2 weeks from surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: - 1) Patients 18 years and older 2) Buccal recession defects classified as either Miller class I or II gingival recession. 3) 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 . 7) Teeth with cervical restorations, abrasion
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Azza Ezzelarab
Organizational Affiliation
Professor of periodontics, Faculty of dentistry, Cairo university
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Noha Ghallab
Organizational Affiliation
Professor of periodontics, Faculty of dentistry, Cairo university
Official's Role
Study Director
Facility Information:
Facility Name
Faculty of dentistry
City
Cairo
ZIP/Postal Code
12345
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
12516830
Citation
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Citation
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Use of Platelet Rich Fibrin in Addition to CAF and SCTG for Treatment of Gingival Recession

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