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Pain evaluation after one time root canal treatment in patients with irreversible pulpitis using two different rotating instruments- A Randomised controlled trial.

Not Applicable
Conditions
Health Condition 1: null- patients suffering with symptomatic irreversible pulpitis with deep caries lesion involving pulp
Registration Number
CTRI/2015/02/005487
Lead Sponsor
arayana Dental College and Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Single rooted teeth with irreversible pulpitis with normal periapical radiographic appearance

2.Prolonged response of pain even after the removal of stimulus

3.No signs of periapical lesion or radiolucency

4.patient who has ability to understand the use of pain scales will be provided informed consent for endodontic treatment

Exclusion Criteria

1.patients with sinus tract, periapical abscess or facial cellulitis

2.patient with known allergies or any contraindication to opioid and non opioid analgesics

3.patients with known allergy to local anaesthesia sodium hypochlorite and chlorhexidine

4.presence of systemic diseases like cardio vascular disease, renal disease and any bleeding disorder within last month

5.pregnant and lactating mothers

6.patients who are unable to complete the pain questionnaries

7.patients who are unwilling to sign the informed consent

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
post operative pain evaluation using verbal descriptor scaleTimepoint: post operative pain evaluation using verbal descriptor scale at 8hrs,24hrs and 48hrs.
Secondary Outcome Measures
NameTimeMethod
nilTimepoint: 0
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