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A post-operative pain evaluation with Ultrasonic activation and laser irradiation using continuous chelation irrigant solution in symptomatic irreversible pulpitis teeth A Randomized Clinical Study

Phase 4
Conditions
Health Condition 1: 8- Other Procedures
Registration Number
CTRI/2024/05/067190
Lead Sponsor
Dr Vinaya Pisal
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Healthy patients (Category: American Society of Anaesthesiologists class 1) (ASA House of Delegates 2014) aged between 18 – 60 years of age will be included.

2.maxillary or mandibular teeth diagnosed with Symptomatic irreversible pulpitis with or without periapical pathology or radiographic rarefaction.

3.Only those patients ready to sign the consent form will be included in the study.

Exclusion Criteria

1.Teeth with open apex, root resorption and calcified pulp chamber and canals will be excluded from the study.

2.Teeth with curvature more than 20 degree will be excluded from the study

3.patients taking analgesics 12 hours before the intervention.

4.Teeth which had received previous endodontic treatment will be excluded from the study.

5.Cases showing periodontal pockets deeper than 4mm will be excluded from the study.

6.Teeth with pre-op swelling, draining sinus and Flare ups during root canal treatment will be excluded from the study.

7.Any other iatrogenically affected root canal treatments will be excluded from the study.

8.Medically compromised patients will be excluded from the study.

Study & Design

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