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Study identifier: NCT06671743 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Premedication on Post-endodontic Pain

Condition: Premedication  ·  Sponsor: Gulf Medical University

PhasePhase 3
Planned participants48
Who can joinAll sexes, 20 Years to 50 Years
Healthy volunteersYes

About this study

The goal of this clinical trial is to compare the efficacy of preoperative administration of alpha-chemo-trypsin, ibuprofen, and acetaminophen in managing post-endodontic pain in patients with symptomatic irreversible pulpitis. The main question it aims to answer is: What is the efficacy of preoperative administration of alpha-chemo-trypsin, ibuprofen, and acetaminophen in managing post-endodontic pain in patients with symptomatic irreversible pulpitis? Participants will undergo root canal treatment after premedication. Researchers will compare \[alpha-chemo-trypsin, ibuprofen, and acetaminophen\] to see the intensity of post-endodontic pain.

This description comes directly from the study's public registry record.

Talk to the study team

Elsewify  ·  +971585078876  ·  dr.tarek@gmu.ac.ae

Always discuss trial participation with your own doctor first.

Locations (1)

Gulf Medical UniversityAjman, United Arab EmiratesRecruiting

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Source record: clinicaltrials.gov/study/NCT06671743