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Effect of Periodontal Treatment on the Biomechanical Properties of the Periodontium.

The Effect of Non-surgical Periodontal Treatment on the Biomechanical Properties of the Periodontal Tissues, a Prospective Comparative Clinical Trial.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04646265
Enrollment
30
Registered
2020-11-27
Start date
2017-10-01
Completion date
2022-09-01
Last updated
2023-03-28

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

Conditions

Periodontal Diseases

Keywords

Biomechanics, non-surgical periodontal treatment

Brief summary

Investigation of the biomechanical properties of the periodontal tissues in patients with periodontal disease. Non-surgical periodontal therapy will be assessed between baseline and 30 post-op by general clinical measurements (KT, PPD, CAL, BOP) as well as by biomechanical analysis and compared.

Detailed description

The study is designed as a prospective single center comparative clinical trial to investigate the biomechanical properties of the periodontal tissues in 30 patients with periodontal disease. Success of non-surgical periodontal therapy between baseline and 30 post-op will be assessed by general clinical measurements (KT, PD, CAL, BOP) as well as by biomechanical analysis. Besides assessment for regular treatment effectiveness, safety parameter such as wound healing and adverse events will be assessed. Additionally 10 periodontally healthy persons without local inflammation and bone loss shall be monitored and used a control group for reference to the test teeth.

Interventions

OTHERperiodontal treatment

non-surgical root debridement

Sponsors

University of Bonn
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

prospective single center comparative clinical trial to investigate the biomechanical properties of periodontal tissues

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Moderate/advanced/severe periodontitis * Intact anterior dentition upper yaw. * Expected performance of adequate oral hygiene * Subjects must have voluntarily signed the informed consent form before any study related procedures * Males and females with at least 18 years of age * Subjects must be committed to the study and the required follow-up visits * Subject must be judged in good general health as assessed by the investigator at time of non-surgical therapy

Exclusion criteria

* Any contraindications for subgingival instrumentation * Uncontrolled diabetes or other uncontrolled systemic diseases * Disorders or treatments that compromise wound healing * Medical conditions requiring chronic high dose steroid therapy * Bone metabolic diseases * Radiation or other immuno-oppressive therapy * Chronic anti-inflammatory treatment (≥3 times per week) within 4 weeks prior to treatment * Presence of oral lesions (such as ulceration, malignancy) * Mucosal diseases (e.g., lichen planus, mouth ulcer) * History of malignant disease in the oral cavity or previous radiotherapy to the head or neck * Treatment with an investigational drug or device within the 30 day period immediately prior to therapy on study day 0 * Female subjects who are nursing, pregnant, or plan to become pregnant * Antibiotic treatment

Design outcomes

Primary

MeasureTime frameDescription
Probing depth (PPD) at test tooth3 monthsmean PPD (mm)
Bleeding on Probing (BoP)3 monthsmean BoP (%)
Clinical attachment level (CAL)3 monthsmean attachment level (mm)
Biomechanical analysis3 monthsTooth displacement (mm)

Secondary

MeasureTime frameDescription
4.General Oral Health Assessments Indices (GOHAI)3 monthsProblems to speak clearly - Questionaire by visual analogue scale (VAS)
5.General Oral Health Assessments Indices (GOHAI)3 monthsDiscomfort when eating any kind of food - Questionaire by visual analogue scale (VAS)
6.General Oral Health Assessments Indices (GOHAI)3 monthsLimit contact with people - Questionaire by visual analogue scale (VAS)
7.General Oral Health Assessments Indices (GOHAI)3 monthsPleased with look of teeth- Questionaire by visual analogue scale (VAS)
3.General Oral Health Assessments Indices (GOHAI)3 monthsProblems to swallow comfortably - Questionaire by visual analogue scale (VAS)
9.General Oral Health Assessments Indices (GOHAI)3 monthsWorried about teeth, gums or dentures - Questionaire by visual analogue scale (VAS)
10.General Oral Health Assessments Indices (GOHAI)3 monthsSelf-conscious of teeth, gums or dentures - Questionaire by visual analogue scale (VAS)
11.General Oral Health Assessments Indices (GOHAI)3 monthsUncomfortable eating in front of others - Questionaire by visual analogue scale (VAS)
12.General Oral Health Assessments Indices (GOHAI)3 monthsSensitive to hot, cold or sweet foods - Questionaire by visual analogue scale (VAS)
8.General Oral Health Assessments Indices (GOHAI)3 monthsUsed medication to relieve pain- Questionaire by visual analogue scale (VAS)
Biotype/keratinized tissue width (KT)3 monthsmean - keratinized tissue width (KT)
1.General Oral Health Assessments Indices (GOHAI)3 monthsLimit the kinds of food - Questionaire by visual analogue scale (VAS)
2.General Oral Health Assessments Indices (GOHAI)3 monthsTrouble biting or chewing - Questionaire by visual analogue scale (VAS)

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026