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Full-Mouth vs. Quadrant-Wise Scaling and Root Planing: Clinical Effectiveness, Environmental Sustainability, and Patient-Reported Outcomes

COMPARISON OF FULL-MOUTH AND QUADRANT-WISE SCALING AND ROOT PLANING IN TERMS OF CLINICAL EFFECTIVENESS, ENVIRONMENTAL SUSTAINABILITY, AND PATIENT-REPORTED OUTCOMES

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07785115
Enrollment
52
Registered
2026-08-25
Start date
2025-09-15
Completion date
2026-09-01
Last updated
2026-08-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stage III Periodontitis

Keywords

Periodontitis, scaling and root planing, life cycle assessment, patient-reported outcomes, environmental sustainability

Brief summary

This randomized clinical trial compares full-mouth and quadrant-wise scaling and root planing in patients with Stage III periodontitis. In addition to evaluating clinical effectiveness and patient-reported outcomes, the study investigates the environmental sustainability of both treatment protocols using life cycle assessment. The findings are expected to contribute to more sustainable and patient-centered periodontal treatment planning.

Interventions

PROCEDUREFull-Mouth Scaling and Root Planing

Full-mouth scaling and root planing was completed in a single treatment session using ultrasonic scalers and Gracey curettes. Standardized oral hygiene instructions were provided before treatment. Participants were re-evaluated at 1-, 3-, and 6-month follow-up visits, and additional non-surgical periodontal treatment was provided for sites requiring further therapy when clinically indicated.Clinical outcomes, patient-reported outcomes, and the environmental impact of the treatment protocol were assessed throughout the study.

PROCEDUREQuadrant-Wise Scaling and Root Planing

Quadrant-wise scaling and root planing was performed over four treatment sessions scheduled at one-week intervals using ultrasonic scalers and Gracey curettes. Standardized oral hygiene instructions were provided before treatment. Participants were re-evaluated at 1-, 3-, and 6-month follow-up visits, and additional non-surgical periodontal treatment was provided for sites requiring further therapy when clinically indicated. Clinical outcomes, patient-reported outcomes, and the environmental impact of the treatment protocol were assessed throughout the study.

Sponsors

Selcuk University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

Age ≥18 years. Diagnosis of Stage III periodontitis according to the 2017 World Workshop -Classification of Periodontal and Peri-Implant Diseases and Conditions. Presence of at least four teeth in each quadrant, including at least one molar, excluding third molars. Absence of any systemic disease. No regular use of systemic medications. No history of periodontal treatment within the previous 6 months. No use of antibiotics, anti-inflammatory agents, or any other medications that could affect periodontal tissues within the previous 6 months. Non-smokers or individuals who had ceased smoking for at least 1 year prior to enrollment. Not pregnant or breastfeeding.

Exclusion criteria

Age \<18 years. Presence of any systemic disease. Regular use of systemic medications. History of periodontal treatment within the previous 6 months. Failure to complete the treatment protocol or attend scheduled follow-up visits. Current smoking. Use of antibiotics, anti-inflammatory agents, or any other medications that could affect the periodontal tissues within the previous 6 months. Requirement for antibiotic prophylaxis prior to dental treatment.

Design outcomes

Primary

MeasureTime frameDescription
Probing Pocket Depth (PPD)Baseline, 1 month, 3 months, and 6 monthsMean probing pocket depth (PPD) was measured at six sites per tooth using a manual periodontal probe and recorded in millimeters (mm). Lower PPD values indicate improved periodontal status.

Secondary

MeasureTime frameDescription
Clinical Attachment Level (CAL)Baseline, 1 month, 3 months, and 6 monthsMean clinical attachment level (CAL) was measured at six sites per tooth using a manual periodontal probe and recorded in millimeters (mm). Lower CAL values indicate improved periodontal attachment.
Bleeding on Probing (BOP)Baseline, 1 month, 3 months, and 6 monthsBleeding on probing (BOP) was assessed by recording the presence or absence of bleeding within 30 seconds after gentle periodontal probing at the buccal, lingual/palatal, mesial, and distal surfaces of each tooth. Results were expressed as the percentage (%) of bleeding sites, with lower values indicating reduced gingival inflammation.
Plaque Index (PI)Baseline, 1 month, 3 months, and 6 monthsPlaque Index (PI) was assessed on all teeth according to the Silness and Löe index and recorded as a mean index score. Lower PI scores indicate better plaque control.
Gingival Index (GI)Baseline, 1 month, 3 months, and 6 monthsGingival Index (GI) was assessed on all teeth according to the Löe and Silness index and recorded as a mean index score. Lower GI scores indicate reduced gingival inflammation.
Periodontal Inflamed Surface Area (PISA)Baseline, 1 month, 3 months, and 6 monthsPeriodontal Inflamed Surface Area (PISA) was calculated using a validated method based on clinical attachment level, gingival recession, and bleeding on probing measurements and recorded in square millimeters (mm²). Lower PISA values indicate a reduced periodontal inflammatory burden.
Periodontal Epithelial Surface Area (PESA)Baseline, 1 month, 3 months, and 6 monthsPeriodontal Epithelial Surface Area (PESA) was calculated from clinical attachment level and gingival recession measurements and recorded in square millimeters (mm²). Lower PESA values indicate a smaller periodontal epithelial surface area.
Pain Intensity (Visual Analog Scale, VAS)At the 1-month follow-up visitPain intensity following periodontal treatment was assessed using a 10-cm Visual Analog Scale (VAS), where 0 represented no pain and 10 represented the worst imaginable pain. Lower VAS scores indicate lower perceived pain intensity.
Oral Health-Related Quality of Life (OHIP-14)At the 1-month follow-up visitOral health-related quality of life was assessed using the Oral Health Impact Profile-14 (OHIP-14) questionnaire.
Analgesic UseAt the 1-month follow-up visitThe number of participants who reported using or not using analgesic medication following periodontal treatment was recorded for each treatment group.
Preference for Future Periodontal TreatmentAt the 6-month follow-up visitAt the 6-month follow-up visit, participants were asked whether, based on their experience with the assigned treatment approach, they would prefer the alternative periodontal treatment approach if future periodontal treatment were needed. Responses were recorded for analysis.
Environmental Impact of Periodontal Treatment ApproachesDuring the 6-month study periodThe environmental impacts of the periodontal treatment approaches were assessed using Life Cycle Assessment (LCA).

Countries

Turkey (Türkiye)

Contacts

PRINCIPAL_INVESTIGATORSefa Aydındoğan

Department of Periodontology, Faculty of Dentistry, Selcuk University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 26, 2026