Comparing two methods for treating gingival recession
Comparative Evaluation Of the Restorative Capacity Of Marginal Gingiva Using MINST and Conventional Subgingival Instrumentation Involving RT1 Gingival Recession: A Randomized Controlled Clinical Trial
This study is testing whether a gentle, non-surgical treatment for gum recession works better than the traditional method for people with localized and shallow gum issues.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 54 (estimated) |
| Ages | 20 Years to 50 Years |
| Sex | All |
| Sponsor | Postgraduate Institute of Dental Sciences Rohtak Academic / other |
| Locations | 1 site (Rohtak, Haryana) |
| Trial ID | NCT06044727 on ClinicalTrials.gov |
What this trial studies
This clinical trial aims to compare the effectiveness of minimally invasive non-surgical periodontal therapy (MINST) against conventional subgingival instrumentation in treating Type 1 gingival recession. The study focuses on patients with localized and shallow gingival recession, assessing how each method impacts the restorative capacity of the marginal gingiva. By utilizing delicate instruments and magnifying loupes, MINST seeks to enhance calculus and biofilm removal while minimizing soft tissue trauma. The trial will evaluate clinical outcomes to determine which approach yields better results for patients.
Who should consider this trial
Good fit: Ideal candidates for this study are systemically healthy individuals aged 20 to 50 with Type 1 gingival recession of 3mm or less.
Not a fit: Patients with systemic diseases, pregnant women, smokers, or those with a history of periodontal surgery in the affected area may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could lead to improved treatment options for patients with gingival recession, enhancing healing and clinical outcomes.
How similar studies have performed: While there is limited research directly comparing MINST to conventional methods, studies have shown success with non-surgical periodontal therapies in managing gingival recession.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: 1. Gingival Recession Type 1(RT1) by Cairo et al 2011in esthetic zone including maxillary and mandibular anteriors and premolars, otherwise systemically healthy 2. Gingival Recession ≤3mm associated with plaque induced inflammation and identifiable CEJ 3. Age 20 years to 50 years 4. Providing a written and verbal informed consent. Exclusion Criteria: 1. Patient with systemic disease that can influence the outcome of therapy. 2. Pregnant females or on oral contraceptive pills or hormone replacement therapy. 3. Smokers and patients undergoing orthodontic therapy 4. Physically and mentally impaired patients. 5. Non vital, mal-positioned tooth 6. Presence of cervical abrasions or restorations in the area 7. Previous history of periodontal surgery on the involved sites.
Where this trial is running
Rohtak, Haryana
- Post Graduate Institute of Dental Sciences — Rohtak, Haryana, India (Recruiting)
Study contacts
- Principal investigator: Anjali Yadav, BDS — Postgraduate Institute of Dental Sciences Rohtak
- Study coordinator: Dr. Nishi Tanwar, MDS
- Email: nsh_tanwar@yahoo.com
- Phone: 8368126310
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.