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Evaluation of the levels of immune response in teeth that have undergone cell death after placing simvastatin as an root canal medicine.

Phase 4
Completed
Conditions
Health Condition 1: K041- Necrosis of pulp
Registration Number
CTRI/2022/08/044749
Lead Sponsor
SRM Dental College
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
34
Inclusion Criteria

ASA score 1

Healthy patients aged 16-60 years

patients diagnosed with pulpal necrosis and symptomatic apical periodontitis (PAI =2)

Single rooted teeth with single canal and closed apex

Exclusion Criteria

Patients under ASA 2-5 category.

Patients under any medication for a week.

Patients with periapical pathology (PAI score >2)

Teeth with cracks, vertical root fracture, internal & external resorption.

Multirooted teeth, Single rooted teeth with multiple canals.

Teeth with immature apex.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Quantification and comparison of <br/ ><br>Interleukin-6 before and after <br/ ><br>placement of simvastatin will show <br/ ><br>decrease in its concentrationTimepoint: Samples will be taken before and after biomechanics preparation and after 7 days of intracanal medication placement.
Secondary Outcome Measures
NameTimeMethod
Quantification and comparison of <br/ ><br>Interleukin-6 before and after <br/ ><br>placement of Calcium hydroxide will <br/ ><br>show decrease in its concentration.Timepoint: Samples will be taken before and after biomechanics preparation and after 7 days of intracanal medication placement.
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