- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05449938
Periodontal Phenotype and Scaling and Root Planing
Clinical Evaluation of Impact of Periodontal Phenotype on the Outcome of Scaling and Root Planing in Patients With Periodontitis: A Comparative Interventional Study
Periodontal phenotype has been recognized as one of the key factors that may potentially impact the outcome of a variety of periodontal surgical and non-surgical procedures. Taking into consideration the inconsistent findings of the studies done in this regard,outcomes of scaling and root planing with respect to periodontal phenotype.
With this aim, the present study would be conducted to assess the influence of periodontal phenotype on outcome of scaling and root planing in periodontitis patients.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
AIM: To evaluate the influence of periodontal phenotype on the outcomes of scaling and root planing in periodontitis patients.
OBJECTIVES:
To assess the improvement in pocket probing depth (PPD), clinical attachment level (CAL), bleeding in pocket probing (BOPP), bleeding on marginal probing (BOMP), gingival marginal position (GMP), gingival recession (GR), plaque index (PI), and gingival index (GI) after scaling and root planing (SRP) in periodontitis patients with thin or thick periodontal phenotype.
SETTING: Department of periodontics and oral implantology, PGIDS, Rohtak, Haryana.
STUDY DESIGN: Comparative Interventional study.
TIME FRAME: 12 months (september 2021- August 2022)
POPULATION:
Systemically healthy patients with periodontitis (periodontitis stage II and stage III) and thin/thick periodontal phenotype in maxillary and mandibular incisors will be included.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: RAJINDER KR SHARMA, MDS
- Phone Number: 9416358222
- Email: rksharmamds@yahoo.in
Study Locations
-
-
Haryana
-
Rohtak, Haryana, India, 124001
- Recruiting
- Post Graduate Institute of Dental Science
-
Contact:
- Ambika Gupta, MDS
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Systemically healthy patients with periodontitis (periodontitis stage 2 and stage 3) and thin/thick periodontal phenotype in maxillary and mandibular incisors will be included.
Exclusion Criteria:
- Systemic condition known to affect the course of periodontal disease like diabetes mellitus or immunogenic disorders.
- Patient on anti-inflammatory drugs or antibiotics or history of treatment with medication known to influence periodontal status or healing within last 2 years.
- Current or former smoker or use of tobacco in any form
- History of periodontal treatment in last 2 years
- Crowding in anterior teeth.
- Pregnant or lactating females.
- Individuals with restorations on anterior teeth.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Thick periodontal phenotype
Stage II and stage III periodontitis Patient with thick periodontal phenotype will be enrolled using probe transparency method .
|
Scaling and root planing involves removal of plaque and calculus on tooth surface.
|
Active Comparator: Thin periodontal phenotype
Stage II and stage III periodontitis Patient with thin periodontal phenotype will be enrolled using probe transparency method.
|
Scaling and root planing involves removal of plaque and calculus on tooth surface.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Probing pocket depth
Time Frame: 6 months
|
Change in pocket probing depth from baseline to 6 months
|
6 months
|
BLEEDING ON POCKET PROBING (BOPP)
Time Frame: 6 months
|
Change in bleeding on pocket probing depth from baseline to 6 months
|
6 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Krishan Kant, BDS, Post graduate institute of Dental Sciences ROHTAK
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Krishan kant perio
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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