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Evaluating efficiency of combination of analgesics and cryotherapy in pain reduction for root canal therapy.

Phase 4
Conditions
Health Condition 1: K044- Acute apical periodontitis of pulpal origin
Registration Number
CTRI/2023/09/057346
Lead Sponsor
Dr Rajaram S
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

Patients diagnosed with maxillary or mandibular premolars having symptomatic irreversible pulpitis or symptomatic apical periodontitis

Patients with a pre-operative pain score of > 5 on numerical scale

Exclusion Criteria

Patients with systemic disorders that could alter pain perception like diabetes, schizophrenia etc.

Patients with a history of allergies to local anesthesia or analgesic drugs.

Fractured teeth, Endodontically treated teeth, immature apices and external root resorption

Presence of other symptomatic teeth that cause pain and discomfort in patients other than tooth of interest.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Reduction in inter appointment pain levels in patients in ketorol dt irrigant group.Timepoint: 6 hours, 12 hours and 24 hours after intervention <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
Reduction in post obturation pain levels in patients in ketorol dt irrigant group.Timepoint: after obturation - 56 hours, 68 hours & 80 hours
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