Comparison of combination of diclofenac sodium/acetaminophen versus combination of ibuprofen/acetaminophen in pulpal necrosis

Phase 4

• Conditions: Oral and Gastrointestinal - Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon; Pulpal necrosis

• Registration Number: ACTRN12622000320752
• Lead Sponsor: Quratulain Khan

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-02-21
• Last Update Posted: 28 February 2022

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 330

Inclusion Criteria

Teeth with pulpal necrosis having moderate to severe pain at the time of treatment ranging from 5-10 on visual analogue scale VAS (0-10)
Teeth negative to Cold test and Electric pulp tester
Periapical radiograph with minimum 2×2mm radiolucency at the apex

Exclusion Criteria

Patient with history of Gastrointestinal disorder (GIT) disorders, respiratory disorder, decreased hepatic function, hemorrhagic disorder, poorly controlled Diabetes Mellitus, allergic to ibuprofen, diclofenac sodium or acetaminophen, pregnant women and nursing mother.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Method of assessment is Mean pain score using a visual analogue scale VAS form given to patient to mark the score of pain after 6 hour of treatment and bring the form on next appointment.<br><br> [6 hours after the first visit of treatment procedure]

Secondary Outcome Measures

Name	Time	Method
one [None ]