Impact of MINST With & Without Splinting in Periodontitis Patients With

Status Not yet recruiting

Clinical Trial Summary

The goal of this clinical trial is to evaluate impact of Minimally Invasive Non-Surgical Therapy (MINST) with and without splinting on clinical periodontal parameters and Oral Health Related Quality of Life (OHRQoL) in periodontitis patients with mobile anterior teeth. The main questions it aims to answer are: - Does splinting provide additional benefit to MINST alone for improving the clinical periodontal parameters ? - Does splinting provide additional benefit to MINST alone for improving OHRQoL ?

Clinical Trial Description

The increased mobility of a periodontally affected tooth can be caused by a shift of centre of rotation of the tooth apically due to clinical attachment loss (CAL) and alveolar bone loss (ABL) and/or due to secondary occlusal trauma. Tooth splinting continues to be a topic of controversy. It remains one of the most poorly understood and controversial areas of dental therapy. Minimally invasive non-surgical periodontal therapy (MINST) has been introduced for minimizing tissue trauma and enhancing clinical outcomes by the adjunctive use of magnification devices . This study aims to compare clinical periodontal parameters and Oral Health Related Quality of Life (OHRQoL) following Minimally Invasive Non-Surgical Therapy (MINST), both with and without splinting, in patients with Stage III and Stage IV periodontitis who have mobile anterior teeth. Patients will be screened and enrolled based on specific eligibility criteria. Baseline measurements of outcome parameters will be taken, followed by supragingival scaling, and patients will be recalled after one week. During the subsequent visit, patients will be randomized into either the test group or the control group. The test group will receive MINST along with splinting of the mobile anterior teeth, while the control group will receive MINST alone. Patients will be recalled after 8 weeks and 6 months to assess changes in the outcome measurements. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06436729
Study type	Interventional
Source	Postgraduate Institute of Dental Sciences Rohtak
Contact	Ritika Arora, MDS
Phone	9810734445
Email	drritika44@gmail.com
Status	Not yet recruiting
Phase	N/A
Start date	June 1, 2024
Completion date	December 31, 2025

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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 MINST With and Without Splinting in Periodontitis Patients With Mobile Anterior Teeth

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms