MedPath

PAIN AFTER ROOT CANALAFTER USING 2 DIFFERENT FILLING MATERIA

Phase 2
Conditions
Health Condition 1: K040- Pulpitis
Registration Number
CTRI/2022/11/047184
Lead Sponsor
SHREYA SIVASAILAM
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Subjects having a mandibular molar tooth with Chronic irreversible pulpitis with no signs of apical periodontitis needing primary endodontic treatment.

Cooperative health subjects who are willing to participate in the study and sign the consent form.

Exclusion Criteria

-Subjects with uncontrolled systemic diseases or allergies.

-History of previous root canal treatment.

-Presence of swelling or sinus tracts.

-Presence of severe periodontal disease.

-Periapical radiolucency.

-Subjects whoâ??ve taken analgesics within the last 3 days.

-Subjects allergic to local anesthesia.

-Subjects unwilling to sign the consent form.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
POST OPERATIVE PAIN MEASUREMENT USING VISUAL ANALOG SCALETimepoint: 7 DAYS
Secondary Outcome Measures
NameTimeMethod
ANALGESICS TAKEN IF ANYTimepoint: 7 DAYS
© Copyright 2025. All Rights Reserved by MedPath