Effectiveness of Scaling and Root Planing in Deeper Pockets

NCT ID: NCT06890689

Last Updated: 2025-12-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ACTIVE_NOT_RECRUITING

Total Enrollment

110 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-01-01

Study Completion Date

2026-08-01

Brief Summary

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This study will retrospectively evaluate the outcomes of scaling and root planing over a two year time period. The study will focus specifically on the effectiveness of SRP in pockets with an initial pre-treatment pocket probing depth of ≥ 5 mm and ≤ 8 mm. The study will also examine the response to SRP of all initial pocket depths, i.e., those PPD that fall below or above those in the indicated range, to verify the findings of previous studies.

Detailed Description

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Conditions

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Periodontal Disease Periodontitis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Patients received SRP at predoctoral clinic

Scaling and root planing

Intervention Type PROCEDURE

Retrospective study to evaluate the outcome of scaling and root planing

Interventions

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Scaling and root planing

Retrospective study to evaluate the outcome of scaling and root planing

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* All patients treated by dental students who have the required data
* 14 or more permanent teeth
* Have at least 2 molars (excluding third molars)

Exclusion Criteria

* All third molars and second molars next to a partially impacted third molar
* Smokers
* Diabetes
* Immunocompromised patients (HIV/AIDS; chemotherapy; systemic steroid therapy, etc.)
* Pregnancy during treatment or during the follow-up periods
* Diagnosis of Alzheimer's or dementia
* Diagnosis of oral mucous membrane disease (BMMP, Lupus, erosive lichen planus, etc.)
* Patients that have received periodontal surgery following SRP
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Texas A&M University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Texas A&M University Collage of Dentistry,

Dallas, Texas, United States

Site Status

Countries

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United States

Other Identifiers

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Effectiveness of SRP

Identifier Type: -

Identifier Source: org_study_id

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