MedPath

To find out the effectiveness of sodium alendronate gel in flap surgery with laser therapy

Phase 2
Conditions
Health Condition 1: K053- Chronic periodontitis
Registration Number
CTRI/2024/07/071279
Lead Sponsor
ITS Dental College Hospital and Research Centre Greater Noida
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Patients aged from 25 to 50 year both gender

2.Patients afflicted with Chronic Periodontitis as per (AAP classification 2017) with Probing depth- = to 4mm and = 7mm

3.Radiographic evidence of bone loss(horizontal/vertical).

4.No usage of antibiotics in the preceding 6 months of the study

Exclusion Criteria

1.Allergic to Alendronate/Bisphosphonate group of drugs

2.Systemic Alendronate / Bisphosphonate group of drugs therapy.

3.Smokers and tobacco chewers.

4.Immunocompromised patients.

5.Pregnant and lactating women

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.To evaluate the clinical efficacy of 1% topical application of Sodium Alendronate gel in open flap debridement of surgical management in Chronic Periodontitis. <br/ ><br> <br/ ><br>2.To evaluate the effect of 1% topical sodium alendronate gel in open flap debridement with laser bio stimulation. <br/ ><br>Timepoint: Base line, 7days, 1month, 6 month
Secondary Outcome Measures
NameTimeMethod
1.To compare and evaluate the effect of laser bio stimulation in open flap debridement. <br/ ><br> <br/ ><br>2. To assess and compare the effect of diode laser therapy on gingival clinical parameters. <br/ ><br> <br/ ><br>Timepoint: Base line, 7days, 1month, 6 month
© Copyright 2025. All Rights Reserved by MedPath