Impact of Subgingival Instrumentation on Masticatory Performance &

Status Recruiting

Clinical Trial Summary

Patients of Stage III and Stage IV Periodontitis will be assessed for masticatory dysfunction and psychological distress. Subgingival Instrumentation will be done for treating periodontitis. Patients will be re-evaluated after 2 and 3 months in order to assess any change in masticatory dysfunction and psychological distress by improved periodontal health.

Clinical Trial Description

Literature reveals that there occurs masticatory dysfunction in patients with Stage III and IV Periodontitis. It has been hypothesized that masticatory dysfunction along with halitosis and aesthetics of the patient can have an effect on the psychological distress in a chronic state. Patients of Stage III and Stage IV Periodontitis with the following criteria will be included : 1. Adult patients with age group 30-50 years diagnosed with stage III/IV generalized periodontitis. 2. Presence of minimum 20 teeth (Eichner group A1, A2, A3) excluding third molars. Exclusion Criteria: Patients with 1. Systemic diseases that may affect periodontal disease progression or outcome of treatment (diabetes, autoimmune diseases) 2. Systemic diseases that may affect masticatory ability of the patient (sarcopenia, TMJ disorders, Xerostomia, Acute Pulpitis) 3. History of periodontal treatment within the 6 months 4. Patients wearing orthodontic appliances 5. Diagnosed psychiatric disorder 6. History of antibiotic use within the previous 3 months 7. History of use of Steroid, immunosuppressive and psychiatric drugs 8. Pregnant and lactating women 9. Smoking or substance abuse 10. History of Menopause Periodontal clinical parameters: Plaque Index, Gingival Index, Bleeding on Probing, Probing Pocket Depth, Clinical Attachment Level, Mobility Psychological Parameters: Hospital Anxiety and Depression Scale -14 and Depression Anxiety and Stress Scale -21 Quality of Masticatory Dysfunction Questionnaire and Objective evaluation of Masticatory Performance by mixing ability of Hubba Bubba chewing gum. The sample of 84 patients consisting of 42 cases and 42 controls. The patients will be re-evaluated at 2 and 3 months follow up for clinical periodontal parameters, masticatory performance and psychological distress. ;

Study Design

Related Conditions & MeSH terms

Periodontitis

Clinical Trial Details

NCT number	NCT06024447
Study type	Interventional
Source	Postgraduate Institute of Dental Sciences Rohtak
Contact	Sanjay Tewari, MDS
Phone	91-1262-283876
Email	principalpgids@yahoo.in
Status	Recruiting
Phase	N/A
Start date	September 15, 2023
Completion date	October 15, 2024

View Details

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

Impact of Subgingival Instrumentation on Masticatory Performance and Psychological Distress

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms