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

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

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

48 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-07-01

Study Completion Date

2025-12-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Non-surgical periodontal treatment is a fundamental part of periodontal therapy,including supportive therapy. It has been proven to be efficacious in reducing inflammation, probing pocket depth and number of diseased sites in patients affected by periodontitis, often limiting the need for additional treatment approaches. However,despite being such a widely administered treatment, the effect of non-surgical periodontal treatment on patient reported outcomes has remained restricted to parameters such as pain and sensitivity only, with patient's perception of aesthetics remaining largely unexplored.

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.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Periodontal disease refers to inflammation of the periodontal tissues resulting in clinical attachment loss, alveolar bone loss and periodontal pocket formation. Periodontal disease is amongst one of the most common diseases affecting majority of the population around the world. Patients with periodontal diseases may present with bleeding, redness, swelling or edema in the gingiva, gingival recession, gingival enlargement, loss of the supporting periodontal tissues and tooth mobility. All these conditions affecting the periodontium are detrimental for individual's quality of life and may also disrupt their esthetic appearance. A number of factors are substantial for dental esthetics such as color and shape of the teeth and shape of the dental arch. However, gingival health and appearance is also crucial for an esthetically pleasant smile and patients with periodontal problems may face aesthetic problems. Gingival recessions in the anterior teeth can often be a topic of concern, and this non-aesthetic appearance can be observed within the patient's smile, speech or chewing. Localized or generalized gingival enlargement may also result in both aesthetic and functional problems for affected patients. Additionally, the color of gingiva as well excess gingival display can pose esthetic concerns.

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

See the medical conditions and disease areas that this research is targeting or investigating.

Periodontitis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NA

Intervention Model

SINGLE_GROUP

The study population will include consecutive subjects referred to the Department of Periodontics, PGIDS, Rohtak for clinical evaluation. The patients will be screened according to the inclusion and exclusion criteria for eligibility to participate in the study. All participants will be informed about the purpose of the study and only individuals who provide written informed consent prior to the start of the study will be included.

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.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

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.

Group Type EXPERIMENTAL

non-surgical periodontal therapy

Intervention Type PROCEDURE

change in self perception of esthetics and clinical periodontal parameters will be assessed after non-surgical periodontal therapy.

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

non-surgical periodontal therapy

change in self perception of esthetics and clinical periodontal parameters will be assessed after non-surgical periodontal therapy.

Intervention Type PROCEDURE

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

scaling and root planing

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Patients in the age group of (18-60 years).
* 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

* Smokers.
* 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.
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Postgraduate Institute of Dental Sciences Rohtak

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Ayesha Ahmed

Role: PRINCIPAL_INVESTIGATOR

PGIDS, Rohtak

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Post Graduate Institute of Dental Sciences

Rohtak, Haryana, India

Site Status

Countries

Review the countries where the study has at least one active or historical site.

India

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Dr.Aditi Sangwan

Role: CONTACT

9996002408

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

Ayeshaperio_12

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.