Gingival Recession Clinical Trial
Official title:
Comparative Evaluation of rhPDGF- BB With Modified Coronally Advanced Tunnel and CTG Versus Modified Coronally Advanced Tunnel With CTG Alone for Root Coverage in Multiple Mandibular Gingival Recession Defects- A RCT
NCT number | NCT03676088 |
Other study ID # | 02_D012_71663 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | November 2016 |
Est. completion date | July 2018 |
Verified date | September 2018 |
Source | Krishnadevaraya College of Dental Sciences & Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The present study is a human, prospective, single centre, single blind, comparative controlled randomized clinical trial for the treatment of Miller's Class I, II or combination of class I and II mandibular recession and comparing the clinical outcomes prior to and 6 months after treatment. The trial is in accordance to the Consolidated Standards of Reporting Trials (CONSORT) criteria, 2010.
Status | Completed |
Enrollment | 6 |
Est. completion date | July 2018 |
Est. primary completion date | July 2018 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 21 Years to 58 Years |
Eligibility |
Inclusion Criteria: - Patients fulfilling the following criteria were included in the study:- - Two or more teeth with Miller's class I and II or combined class I and II recession defects in mandibular anteriors. - Age group 21-58 years. - Patients with healthy or treated periodontal conditions. - Patients willing to participate in the study. - Absence of uncontrolled medical conditions. - Patients with full mouth plaque score </= 10%(O'Leary 1972) - Patients with esthetic concerns. - Patients with thick gingival biotype >0.8mm Exclusion Criteria: - Pregnant or lactating females. - Tobacco smoking. - Uncontrolled medical conditions. - Untreated periodontal conditions. - Use of systemic antibiotics in the past 3 months. - Patients treated with any medication known to cause gingival hyperplasia. - Drug and alcohol abuse - No occlusal interferences. - Patient with a known hypersensitivity to rhPDGF-BB. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Krishnadevaraya College of Dental Sciences & Hospital |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Gingival recession depth (GRD) | measured as the distance from the Cemento Enamel Junction to the gingival margin | 6 months | |
Primary | 2. Gingival Recession Width (GRW) | measured as the distance between the mesial gingival margin and distal gingival margin | 6 months | |
Primary | Mean root coverage(MRC) | (Baseline recession depth - 6 month recession depth/Baseline recession depth)*100 | 6 months | |
Primary | Complete root coverage(CRC) | root coverage regarded as complete with gingival margin located at the level of Cemento Enamel Junction | 6 months | |
Primary | coverage esthetic score(RCES) | The Aesthetic evaluation was performed according to the root coverage aesthetic score system (RES) Five Variables evaluated which are as follows: Level of Gingival margin (GM) Marginal Tissue Contour (MTC) Soft Tissue Texture (STT) Mucogingival Junction(MJ) alignment Gingival Colour (GC) |
6 months | |
Secondary | probing pocket depth (PD) | measured as the distance from the gingival margin to the base of gingival sulcus | 6 months | |
Secondary | clinical attachment level (CAL) | measured as Gingival Recession Depth + Probing Depth | 6 months | |
Secondary | width of keratinized tissue (KTW) | measured as the distance from the mucogingival junction to the gingival margin , with the mucogingival junction location determined using a visual method (Schiller's Potassium Iodide Solution). | 6 months |
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