drugset / Trial / NCT03944629

Efficacy of Arnica Montana in Reducing Postoperative Edema and Pain

NCT03944629

Completed 53 enrolled Tufts University
RandomizedParallel-groupDouble-blindTreatment

Summary

This study is a prospective, randomized, double-blinded, controlled, clinical trial that evaluates the efficacy of using high potency homeopathic Arnica montana (SinEcch™) during the perioperative period for decreasing swelling and pain after extraction of partial or full/complete bony impacted third molars. The study group will be comprised of subjects who will receive homeopathic Arnica montana (SinEcch™) for perioperative management of edema and pain. The control group will be comprised of subjects who will receive matching SinEcch™ placebo (sugar pill).

Timeline

Start
2018-01-26
Primary completion
2022-06-14
Completion
2022-06-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Arnica montana Traditional medicine (herbal / TCM)

Indications

No indication recorded.