drugset / Trial / NCT07610265

Comparative Evaluation of Transdermal and Oral Drugs for Management of Post-Endodontic Pain

NCT07610265

Phase 4 Completed 80 enrolled Nims University Rajasthan
RandomizedParallel-groupOpen-labelTreatment

Summary

This clinical trial evaluated whether two drugs delivered through transdermal drug delivery systems reduced post-endodontic pain as effectively as two orally administered medications in adult patients undergoing root canal treatment. The study also compared how effectively these medications controlled pain during the first 48 hours after treatment. The study aimed to answer the following questions: Did transdermal drug delivery systems provide pain relief comparable to or better than orally administered medications after endodontic treatment? Did pain intensity differ among the four treatment groups as measured using the Visual Analog Scale (VAS)? The investigators compared two transdermal drug groups with two oral drug groups to identify the treatment that provided better control of post-endodontic pain. Participants: Underwent root canal treatment for symptomatic irreversible pulpitis. Received one of four analgesic interventions consisting of two transdermal patches or two oral medications. Recorded pain intensity using the Visual Analog Scale (VAS) at 6, 12, 24, and 48 hours after treatment.

Timeline

Start
2024-04-18
Primary completion
2025-10-18
Completion
2025-10-18

Drugs

EvaluationDrugModalityDoseRoute
Comparator Diclofenac Other / unclassified 50 mg Oral
Comparator Fentanyl Other / unclassified 25 ug Other
Comparator Ibuprofen Small molecule 400 mg Oral
Comparator Ketoprofen Small molecule 30 mg Other

Indications

No indication recorded.