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Clinical Trial Details — Status: Completed

Administrative data

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

Study information

Verified date September 2018
Source Krishnadevaraya College of Dental Sciences & Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

24 recession defects were selected in patients who were systemically and periodontally healthy, satisfying the determined inclusion criteria. Patients with at least two or more teeth having Miller's class I , II or combination of class I and II mandibular recession defects were included in the study. A detailed, thorough medical and dental history was obtained and each patient was subjected to comprehensive clinical and radiological examination. All patients were informed about the nature of the study, surgical procedure involved, potential benefits and risks associated with the surgical procedure and a written informed consent was obtained from all patients.

The patients were assigned into two treatment groups (test and control). The test group was treated with recombinant human Platelet Derived Growth Factor-BB and Modified Coronally Advanced Tunnel +Connective Tissue Graft whereas the control group was treated by Modified Coronally Advanced Tunnel +Connective Tissue Graft alone.


Recruitment information / eligibility

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.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
root coverage
recession coverage is treated with modified coronally advanced tunnel with connective tissue graft with recombinant human platelet derived growth factor- BB for Experimental: Test group and without recombinant human platelet derived growth factor- BB for Active Comparator: Control group

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Krishnadevaraya College of Dental Sciences & Hospital

Outcome

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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