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Clinical Trials/NCT05449938
NCT05449938
Unknown
Not Applicable

Clinical Evaluation of Impact of Periodontal Phenotype on the Outcome of Scaling and Root Planing in Patients With Periodontitis: A Comparative Interventional Study

Postgraduate Institute of Dental Sciences Rohtak1 site in 1 country60 target enrollmentSeptember 1, 2021
ConditionsPeriodontitis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Periodontitis
Sponsor
Postgraduate Institute of Dental Sciences Rohtak
Enrollment
60
Locations
1
Primary Endpoint
Probing pocket depth
Last Updated
3 years ago

Overview

Brief Summary

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.

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.

Registry
clinicaltrials.gov
Start Date
September 1, 2021
End Date
August 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Eligibility Criteria

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.

Outcomes

Primary Outcomes

Probing pocket depth

Time Frame: 6 months

Change in pocket probing depth from baseline to 6 months

BLEEDING ON POCKET PROBING (BOPP)

Time Frame: 6 months

Change in bleeding on pocket probing depth from baseline to 6 months

Study Sites (1)

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