Comparison of minimal access non-surgical with minimal access surgical procedure to treat gum disease having bone loss around tooth: A clinical study

Comparative clinical and radiographic evaluation of Minimally invasive non-surgical and Minimally invasive surgical therapy in treatment of periodontal intra-bony defect: A randomized clinical trial - Nil

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2025/07/091516

Enrollment

Registered

2025-07-23

Start date

Unknown

Completion date

Unknown

Last updated

2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K053- Chronic periodontitis

Interventions

Intervention1: Minimally invasive non-surgical therapy: Procedure will be performed under local anesthesia without adrenalin. Extensive debridement of the root surface down to the bottom of the period

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patient diagnosed with periodontitis stage 3. 2.Probing pocket depth more than or equal to 6mm with Radiographic intrabony defect depth more than or equal to 3mm at minimum 1 site. 3.Intrabony Defects not associated with furcation involvement. 4.Patient should have 20 teeth along with adjacent teeth to the defect site. 5.Patient with adequate width of attached gingiva.

Exclusion criteria

Exclusion criteria: 1.Smokers (current or in past 5years), alcohol, drug abuse. 2.Medical history including diabetes, hepatic, renal disease, other serious medical conditions or transmittable diseases. 3.Patient on anti-inflammatory or anticoagulant therapy. 4.Systemic antibiotic therapy during the 3 months preceding the baseline exam 5.Pregnant or lactating women 6.Periodontal treatment at the study site within the last 12 months 7.Root canal treated tooth, prosthesis and class 2 restoration containing tooth at defect site and active orthodontic treatment. 8.Osseous lesion other than intrabony defect at defect site.

Design outcomes

Primary

Measure	Time frame
clinical parameters (probing pocket depth and clinical attachment level), radiographic parameters (defect depth and defect width) in periodontal intrabony defects treated with minimally invasive non-surgical and minimally invasive surgical therapy.Timepoint: Base line, 3 months, 6 months	—

Secondary

Measure	Time frame
Plaque index, gingival index, and gingival marginal level in treatment of periodontal intrabony defects with minimally invasive non-surgical therapy and minimally invasive surgical therapy. Timepoint: Base line, 3 months, 6 months;pain perception in periodontitis patients with intrabony defects treated with minimally invasive non-surgical and minimally invasive surgical therapyTimepoint: 1st day and 7th day post surgery.;correlation clinical and radiographic parameters in periodontal intrabony defects when treated with minimally invasive non-surgical and minimally invasive surgical therapy.Timepoint: base line, 3 months, 6 months	—

Measure

Time frame

Plaque index, gingival index, and gingival marginal level in treatment of periodontal intrabony defects with minimally invasive non-surgical therapy and minimally invasive surgical therapy. Timepoint: Base line, 3 months, 6 months;pain perception in periodontitis patients with intrabony defects treated with minimally invasive non-surgical and minimally invasive surgical therapyTimepoint: 1st day and 7th day post surgery.;correlation clinical and radiographic parameters in periodontal intrabony defects when treated with minimally invasive non-surgical and minimally invasive surgical therapy.Timepoint: base line, 3 months, 6 months

—

Countries

India

Contacts

Public ContactDr Sawal Kala

Maharashtra institute of dental sciences and research dental college Latur

sawalkala@gmail.com9422906216

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026