A clinical trail to study the effects of two tablets in patients with tooth ache during root canal treatment.

Not Applicable

• Conditions: Health Condition 1: null- symptomatic irreversible pulpitis

• Registration Number: CTRI/2018/05/013763
• Lead Sponsor: arayana dental college and hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1.The patients have not taken any analgesics for at least 12 hours before enrollment in the study.

2.Patients with symptomatic irreversible pulpitis of any mandibular posterior teeth.

3.Absence of any periapical radiolucency on radiographs, except for a widened periodontal ligament.

Exclusion Criteria

1.Subjects under 18 years of age.

2.Known allergy, sensitivity, or contraindications to any opioid or non-opioid analgesic NSAIDs and local anesthetics.

3.History of active peptic ulcer within the preceding 12 months.

4.Pregnant or nursing women.

5.History of known or suspected drug abuse.

6.Patients who had taken NSAIDs within 12 hours before administration of the study drugs.

7.Patients with a history of significant medical conditions.

8.Patients unable to give informed consent.

9.Patients having pain in more than 1 mandibular posterior teeth

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Evaluation of pain during access opening of Root canal treatment after giving inferior alveolar nerve blockTimepoint: 15 minutes 30 minutes 45 minutes After administration of inferior alveolar nerve block

Secondary Outcome Measures

Name	Time	Method
pain free root canal treatmentTimepoint: after 1hr