Clinical Trial

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

Recruiting Phase 4
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Record status
This record was last updated November 4, 2024 (before its estimated November 30, 2024 completion). Its status may not reflect the trial's current state.
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 suffer greatly from post endodontic treatment pain and have a fear of dental treatments due to the pain. Patients refuse to go to the dentists and neglect oral hygiene care. That's why it is very important to find an effective drug regimen to reduce this post treatment pain. The null hypothesis is that there will be no difference between the efficacy and mean pain scores of Trypsin-chymotrypsin and Naproxen Sodium for post-endodontic treatment pain. Conducted as a triple-blinded, parallel, randomized controlled trial, 100 patients will be randomly assigned to receive either Trypsin-Chymotrypsin or Naproxen sodium following standard root canal therapy. Pain levels will be assessed using a numerical rating scale at 1, 6, 12, and 24 hours post-treatment to evaluate the effectiveness of these two pain management modalities.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2024-08-16.
Trial Details
NCT Number NCT06562816
Lead Sponsor Dow University of Health Sciences
Conditions Effect of Drug
Enrollment 100 participants
Start Date 2024-08-16
Primary Completion 2024-11-30 (estimated)
Study Completion 2025-01-31 (estimated)
Updated on ClinicalTrials.gov 2024-11-04