drugset / Trial / NCT05982392

Effect of Preoperative Tramadol and Naproxen Sodium on Post Operative Pain

NCT05982392

Phase 2/3 Completed 139 enrolled Dow University of Health Sciences
RandomizedParallel-groupTriple-blindPrevention

Summary

The goal of this clinical trial is to compare in Tramadol, Naproxen sodium and Placebo in participants presenting with irreversible pulpitis in their mandibular molar teeth. The main question\[s\] it aims to answer are: * Local anesthetic efficacy and . * Postoperative pain. Participants will receive premedication treatments 60 minutes prior to the local anesthesia administration. Researchers will compare Tramadol, Naproxen sodium and Placebo to evaluate their effects on Inferior alveolar nerve block efficacy and Postoperative pain.

Timeline

Start
2023-03-01
Primary completion
2023-08-15
Completion
2023-08-15

Drugs

EvaluationDrugModalityDoseRoute
Comparator Naproxen Small molecule 550 mg Oral
Comparator Tramadol Other / unclassified 100 mg Oral

Indications