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A clinical trial to study the effects of propolis gel in the management of gum disease.

Phase 3
Conditions
Health Condition 1: K053- Chronic periodontitis
Registration Number
CTRI/2022/03/041407
Lead Sponsor
Dr Lekshmi R
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1)Patients diagnosed with chronic periodontitis.

2)Patients willing to take part in the study.

3)Patients in the age group 30 to 65 years without systemic disease.

4)Patients with atleast 20 natural teeth.

5)Patients with periodontal pocket depth of >4mm to 8mm with radiological evidence of bone loss.

6)No history of allergy.

7)Patients willing to take part in the study, and willing to turn up after 21 days and signed on the informed consent.

Exclusion Criteria

1)Pregnant and lactating women.

2)Teeth with endo-perio lesions.

3)Patients used tobacco or tobacco related products.

4)Patients under antibiotic therapy within 3 months of time period from the study.

5)Patients with h/o systemic diseases that can affect the periodontal status

6)Patients who have undergone periodontal surgery.

7)Patients using mouthwash regularly

8)Patients diagnosed with aggressive periodontitis

9)Patients allergic to propolis

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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