Status:

RECRUITING

Comparing Trypsin-Chymotrypsin and Naproxen Sodium for Post-endodontic Treatment Pain

Lead Sponsor:

Dow University of Health Sciences

Conditions:

Effect of Drug

Eligibility:

All Genders

18-45 years

Phase:

PHASE4

Brief Summary

This study aims to compare the pain reduction efficacy of Trypsin-Chymotrypsin and Naproxen sodium after root canal treatment in patients with symptomatic irreversible pulpitis. A lot of patients suff...

Detailed Description

i. Background Prevention or management of pain, especially after root canal treatment, is of utmost importance to Endodontists. Non-steroidal anti-inflammatory drugs (NSAIDs) have been the most common...

Eligibility Criteria

Inclusion

  • Both male and female, healthy patients (ASA class 1).
  • Patients between the age group of 18-45 years.
  • Patients who are appointed for endodontic treatment.
  • Maxillary or mandibular teeth diagnosed with symptomatic irreversible pulpitis based on delayed responses to vitality tests.

Exclusion

  • Patients who will require emergency dental treatment.
  • Teeth with any form of peri-apical lesion will be excluded.
  • Patient who have taken analgesics within 24 hours prior to the treatment.
  • Patients with known hypersensitivity or allergy to any of the study medications.
  • Patients with any systemic disease such as uncontrolled diabetes, gastric ulcers, bleeding disorders, or cardiovascular problems.
  • Pregnant or lactating women and pediatric patients.

Key Trial Info

Start Date :

August 16 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

January 31 2025

Estimated Enrollment :

100 Patients enrolled

Trial Details

Trial ID

NCT06562816

Start Date

August 16 2024

End Date

January 31 2025

Last Update

November 4 2024

Active Locations (1)

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Dow University of Health Sciences

Karachi, Sindh, Pakistan, 74200