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Effect of pulpal medicine on periodontal healing

Phase 3
Conditions
Health Condition 1: null- Pulpo periodontal lesions
Registration Number
CTRI/2017/05/008660
Lead Sponsor
Shanmugapriya
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
60
Inclusion Criteria

1.Clinical and radiographic diagnosis of a combined endodontic periodontal lesion

2.Probing pocket depth [PPD] >= 6 mm

3.Wide base pocket

4.Pulpal necrosis as confirmed by negative response to cold and electric pulp test

5.Radiographic alveolar bone destruction without apical communication

Exclusion Criteria

1.Younger than 18 years

2.Pregnant, diabetic, or immunocomprimised

3.Smokers and tobacco chewers

4.Grade 3 mobile teeth

5.Unrestorable tooth

6.Patients with aggressive periodontitis

7.History of recent periodontal therapy within the previous 6 months

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1. Probing pocket depth <br/ ><br>2. Clinical attachment level <br/ ><br>3. Bleeding on probing <br/ ><br>Timepoint: Time Frame 6 months <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
Subjective assessment of pain (Dichotomized as yes or no) will be assessed at baseline and during monthly visits. Further assessment of clinical signs of progression of disease like development of abscess, mobility etc will also be assessed.Timepoint: Time Frame : 6 months
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