NCT06890689

Brief Summary

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.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
110

participants targeted

Target at P50-P75 for all trials

Timeline
3mo left

Started Jan 2025

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress85%
Jan 2025Aug 2026

Study Start

First participant enrolled

January 1, 2025

Completed
3 months until next milestone

First Submitted

Initial submission to the registry

March 17, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

March 24, 2025

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2026

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Last Updated

December 9, 2025

Status Verified

October 1, 2025

Enrollment Period

1.4 years

First QC Date

March 17, 2025

Last Update Submit

December 5, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Effectiveness of SRP (scaling and root planing) in pockets with an initial (baseline) pre-treatment pocket probing depth of ≥ 5 mm and ≤ 8 mm

    From January 2020 to January 2025

Study Arms (1)

Patients received SRP at predoctoral clinic

Procedure: Scaling and root planing

Interventions

Retrospective study to evaluate the outcome of scaling and root planing

Patients received SRP at predoctoral clinic

Eligibility Criteria

Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients treated by dental students at TAMU Collage of Dentistry Predoctoral Clinic

You may qualify if:

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

You may not qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Texas A&M University Collage of Dentistry,

Dallas, Texas, 75246, United States

Location

MeSH Terms

Conditions

Periodontal DiseasesPeriodontitis

Interventions

Tooth ExfoliationRoot Planing

Condition Hierarchy (Ancestors)

Mouth DiseasesStomatognathic Diseases

Intervention Hierarchy (Ancestors)

Dental Physiological PhenomenaDigestive System and Oral Physiological PhenomenaDental ScalingDental ProphylaxisPeriodonticsDentistrySubgingival CurettagePreventive Dentistry

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 17, 2025

First Posted

March 24, 2025

Study Start

January 1, 2025

Primary Completion (Estimated)

June 1, 2026

Study Completion (Estimated)

August 1, 2026

Last Updated

December 9, 2025

Record last verified: 2025-10

Data Sharing

IPD Sharing
Will not share

Locations