Comparative Evaluation of Buccal Fat Pad and Subepithelial Connective Tissue Graft (RCT)
Primary Purpose
Gingival Recession
Status
Completed
Phase
Early Phase 1
Locations
Egypt
Study Type
Interventional
Intervention
free fat graft
subepithelial graft
Sponsored by
About this trial
This is an interventional treatment trial for Gingival Recession
Eligibility Criteria
Inclusion Criteria:
- Patients should be above 18 years.
- Patient included in the study will be with Miller class II recession defect.
- Patient having at least 1 mm of residual keratinized tissue.
Exclusion Criteria:
- Patient with Systemic Problem affecting the results of periodontal Therapy.
- Patients having allergy to drugs.
- Pregnant women.
- Patients with any smoking habits.
- Patients having bleeding problems or on anticoagulant therapy.
- Patients having caries or restorations in relation to the treated site.
Sites / Locations
- Ain shams university
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
study group
control group
Arm Description
Use of free fat graft to cover exposed root
use of sub epithelial connective tissue graft to cover exposed root
Outcomes
Primary Outcome Measures
evaluation of root coverage esthetic score
evaluation of root gingival coverage after modified Coronally advanced flap the scale is from 1-4 ... based on degree of coverage the score will be given 1=1005, 2=75%, 3=50%, 4=25%
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04849663
Brief Title
Comparative Evaluation of Buccal Fat Pad and Subepithelial Connective Tissue Graft
Acronym
RCT
Official Title
Comparative Evaluation of Buccal Fat Pad and Subepithelial Connective Tissue Graft in the Treatment of Localized Recession (Randomized Clinical Trial)
Study Type
Interventional
2. Study Status
Record Verification Date
January 2022
Overall Recruitment Status
Completed
Study Start Date
June 24, 2018 (Actual)
Primary Completion Date
January 24, 2021 (Actual)
Study Completion Date
January 24, 2021 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ain Shams University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Compare between Buccal fat pad and subepithelial connective tissue graft in treatment of localized recession.
Primary objective: to evaluate root coverage in terms of gingival thickness and esthetic.
Secondary objective: to evaluate patient satisfaction and postoperative pain.
Detailed Description
Material and Methods
16 patients from outpatient Oral Diagnosis dental clinic will participate in this study.
Patient selection and hospitalization
Prospective randomized clinical trial will be conducted on patients requiring correction of gingival recession. The research will be reviewed by the ethical committee of Faculty of Dentistry Ain Shams University.
Patient Grouping
Patient will be randomly allocated into one of the two groups:
control group (8 patients): will be treated with coronally advanced flap combined with subepithelial Connective tissue graft (SCTG).
Study group(8 patients): will be treated with coronally advanced flap combined with buccal fat pad (BFP).
Preoperative Assessment
For all patients routine radiographic investigations are required. The first phase of therapy formed of oral hygiene measures, scaling, subgingival debridement and correction of any disturbance in occlusion needed. A periodontal evaluation should be done two weeks after phase I therapy.
A stent will be made for each defect with vertical groove located at the mid-labial region to standardize the placement and angulation of probe while taking measurement. All measurements will be taken with a standardized Williams graduated periodontal probe (Hu-Friedy).
Surgical procedure:
Oral antiseptic mouthwash will be used before anaesthetizing the surgical area. A field block anesthesia at the surgical area is given with a lidocaine and epinephrine-containing solution.
a) Recipient site preparation
A split-thickness flap will be reflected by a horizontal incision made at the papilla base, mesial and distal to the recession defects. Two slightly divergent incisions will be released from the end of the previous horizontal incisions with a full-thickness flap starting from margin of the gingiva reaching 3-4 mm after the exposed bone then continue with a split-thickness extending to the alveolar mucosa .
After flap elevation scaling, planing of the exposed root followed by root conditioning with a tetracycline solution (125 mg tetracycline/ml of saline). In the study group sites, previously prepared BFP or a subepihelial CT graft in control group will be applied over the exposed root a single sling suture will fix the flap just coronal to the Cemento-enamel junction (CEJ). Flaps will also be coronally positioned.
b) Donor site:
In study group the buccal vestibule is anesthetized in vicinity of the first and second maxillary molar. The cheek will be retracted laterally and a mucosal incision will be made while leaving a cuff of non- attached mucosa for closure. The incision will be done throughout the mucosa and muscle meanwhile an external pressure will be applied on the skin in the area of the buccal fat pad. After the buccal fat pad exposure, the fascia is pierced with scissors. With a continuous external pressure on the cheeck a long hemostat is used to spread and manipulate the fat. With minimal delicate traction, the protruding portion of the fat pad is gently grasped and pulled outside of the incision then the fat is clamped at the base and the required amount is harvested and excised to be used in donor site. The incision is closed with suture .
The control group will receive SCTG from the palate with a single incision technique .
Postoperatively patients will be covered by Augmentine 1 gm tablets every 12 hours and flagyl 500 mg every eight hours. Analgesics are given in a combined protocol; where ibuprofen 600mg and paracetamol 1gm are alternating. The patient is instructed to use 0.12% chlorhexidine mouthwash three times daily for two weeks.
Methods of assessment
The parameters which should be measured at baseline, 3 and 6 months after surgery:
Plaque index (PI) will be recorded according to Silness and Loe .
Gingival index (GI) will be recorded according to Loe and Silness .
Probing depth (PD).
Clinical attachment level (CAL).
Recession depth (RD).
Recession width (RW).
Percentage of mean root coverage (MRC %) will be calculated as ([RD preoperative - RD postoperative]/RD preoperative) × 100%.
Width of keratinized tissue (WKT).
Gingival thickness (GTH).
Root coverage esthetic score (RES).
Pain level will be assessed by verbal, numeric scale and by recording amount of analgesic intake postoperatively.
Result presentation and statistics
Results will be tabulated and statistically analyzed.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gingival Recession
7. Study Design
Primary Purpose
Treatment
Study Phase
Early Phase 1
Interventional Study Model
Parallel Assignment
Masking
Investigator
Masking Description
single blinded
Allocation
Randomized
Enrollment
16 (Actual)
8. Arms, Groups, and Interventions
Arm Title
study group
Arm Type
Experimental
Arm Description
Use of free fat graft to cover exposed root
Arm Title
control group
Arm Type
Active Comparator
Arm Description
use of sub epithelial connective tissue graft to cover exposed root
Intervention Type
Biological
Intervention Name(s)
free fat graft
Intervention Description
fat harvested from patient will be used to cover exposed root
Intervention Type
Biological
Intervention Name(s)
subepithelial graft
Intervention Description
subepitheial graft harvested from palate
Primary Outcome Measure Information:
Title
evaluation of root coverage esthetic score
Description
evaluation of root gingival coverage after modified Coronally advanced flap the scale is from 1-4 ... based on degree of coverage the score will be given 1=1005, 2=75%, 3=50%, 4=25%
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Patients should be above 18 years.
Patient included in the study will be with Miller class II recession defect.
Patient having at least 1 mm of residual keratinized tissue.
Exclusion Criteria:
Patient with Systemic Problem affecting the results of periodontal Therapy.
Patients having allergy to drugs.
Pregnant women.
Patients with any smoking habits.
Patients having bleeding problems or on anticoagulant therapy.
Patients having caries or restorations in relation to the treated site.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
shehad wael
Organizational Affiliation
Ain Shams University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ain shams university
City
Cairo
ZIP/Postal Code
11757
Country
Egypt
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Comparative Evaluation of Buccal Fat Pad and Subepithelial Connective Tissue Graft
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