drugset / Trial / NCT06193720

The Impact of Arnica Montana Following the Surgical Extraction of Impacted Third Molars

NCT06193720

Completed 10 enrolled Saint-Joseph University
RandomizedParallel-groupTriple-blindTreatment

Summary

Aim: The aim of this study is to evaluate the action of the homeopathic plant Arnica Montana on postoperative edema, pain and trismus after surgical extraction of impacted wisdom teeth. Materials and Methods: The study is a double-blinded clinical trial recruiting patients undergoing surgical extraction of symmetrically impacted maxillary or mandibular third molars (right and left side). Patients receive alternately and randomly the verum (Arnica Montana 12 CH) or the placebo, in the form of capsules, to be taken 1 day prior to surgery and for 7 days postoperatively. Clinical parameters are collected and include: pain score, maximum mouth opening and facial measurements to assess edema's intensity.

Timeline

Start
2022-02-03
Primary completion
2023-08-20
Completion
2023-08-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Arnica montana Traditional medicine (herbal / TCM)

Indications

No indication recorded.