Evaluation of Effect of Non-surgical Periodontal Treatment on Patient's Self Perception of Esthetics
NCT ID: NCT06477510
Last Updated: 2024-06-27
Study Results
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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NOT_YET_RECRUITING
NA
48 participants
INTERVENTIONAL
2024-07-01
2025-12-01
Brief Summary
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Focusing only on physical periodontal measurements, leaves the true impact of periodontitis as well as its treatment on patient's well-being largely under recognized. With the development of the periodontal aesthetics perception scale (PAPS), it is possible to assess the results in a standardized manner.Therefore, the goal of this study (prospective-interventional ) is to to assess the patient's self-perception of aesthetics using a standardized tool after non surgical periodontal treatment and how much of changes in aesthetics are perceived by the patient. This would be helpful in understanding and managing patient expectations. Also, utilizing a standardized tool would reduce heterogeneity bias by providing comparable data between studies for future research on understanding patient preferences.
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Detailed Description
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Until recently, clinical research has been focused mainly on the course of periodontal disease, its diagnosis, development of appropriate treatments, as well as its clinical response. In this context, a real full impact study, which refers to perceptions and satisfaction of patients in relation to the treatment, has historically not been an object of interest in most investigations. However, in recent years, patients' own assessments of dentofacial aesthetics have become an increasingly popular topic, gradually emphasizing on esthetic conditions as perceived by patients.
Therefore, the present study has been designed to evaluate the change in patients' perception of aesthetics post non-surgical periodontal treatment using the PAPS scale, the Numeric rating scale and global rating scale with the aim to explore the effect of non-surgical periodontal treatment in stage I/II/III periodontitis and assess the psychometric properties of PAPS in Indian population, assess the ability of Periodontal aesthetic perception scale to detect difference in patient's perception of aesthetics after non-surgical periodontal therapy and correlate self-reported perception of aesthetics with clinical periodontal parameters (CAL,BOP, PPD, gingival phenotype, gingival recession, interdental papillary height, gingival pigmentation and gingival display).
The present longitudinal study will be conducted in the Department of Periodontics, Post Graduate Institute of Dental Sciences, Rohtak.Translation, adaptation and validation of PAPS (Periodontal aesthetic perception scale) will be done in Indian population by using the questionnaire on patients reporting to department of Periodontics, PGIDS, Rohtak. Following this, systemically healthy patients with Stage I/II/III Periodontitis will be recruited on basis of inclusion and exclusion criteria. For each participant, demographic data like age, sex, level of education, marital status, socio-economic status and area of residence (urban/rural) will be recorded. Assessment of self-perception aesthetics using PAPS score, NRS and Global Transition Scale will be done at baseline. For all patients, periodontal charting will be done from second premolar to second premolar in both maxillary and mandibular arch.
Oral hygiene instructions and mechanical supragingival scaling followed by subgingival instrumentation as needed on case-to-case basis with both ultrasonic scalers as well as hand instruments. No adjunctive chemical oral hygiene aids or antibiotics will be used.
Re- evaluation of patient's perception of esthetics will be done at 4 weeks. Both patients' perception of esthetics and clinical periodontal parameters (clinical attachment level (CAL), probing pocket depth (PPD), bleeding on probing (BOP), plaque index (PI), gingival phenotype, gingival recession, interdental papillary height, gingival pigmentation and gingival display will be re-evaluated at 3 month follow up appointment post non surgical periodontal treatment with ultrasonic scaler or hand instruments as required.
Conditions
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Study Design
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NA
SINGLE_GROUP
After validation of the PAPS scale, patients with Stage I/II/III Periodontitis will be selected, and PAPS score recorded at baseline, then at 4 weeks and 3 month post non-surgical periodontal treatment and clinical parameters recorded at baseline and 3 month post non-surgical periodontal treatment with ultrasonic scaler or hand instruments as required.
TREATMENT
NONE
Study Groups
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Test group
self perception of esthetics and clinical periodontal parameters will be evaluated in patients with stage I/II/III periodontitis at baseline and post non surgical periodontal therapy.
non-surgical periodontal therapy
change in self perception of esthetics and clinical periodontal parameters will be assessed after non-surgical periodontal therapy.
Interventions
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non-surgical periodontal therapy
change in self perception of esthetics and clinical periodontal parameters will be assessed after non-surgical periodontal therapy.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Presence of ≥ 18 natural teeth
* Ability and willingness to give written informed consent
* Patients belonging to Stage I/II/III periodontitis.
* Systemically healthy individuals.
Exclusion Criteria
* Patients who have received periodontal treatment within 6 months or taken antibacterial drugs within last 3 months.
* Patient with psychological or systemic disease that can influence the outcome of non-surgical periodontal therapy.
* Presence of tooth loss or caries or prosthesis of any type in anterior teeth.
* Pregnant females or on oral contraceptive pills or hormone replacement therapy.
* Physically and cognitively impaired patients.
* Teeth with need for endodontic treatment.
* Teeth with Endo-perio lesion.
* Patients with no aesthetic concerns.
18 Years
60 Years
ALL
No
Sponsors
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Postgraduate Institute of Dental Sciences Rohtak
OTHER
Responsible Party
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Principal Investigators
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Ayesha Ahmed
Role: PRINCIPAL_INVESTIGATOR
PGIDS, Rohtak
Locations
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Post Graduate Institute of Dental Sciences
Rohtak, Haryana, India
Countries
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Central Contacts
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Other Identifiers
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Ayeshaperio_12
Identifier Type: -
Identifier Source: org_study_id
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