Clinical Trials Directory

Trials / Completed

CompletedNCT06193720

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

The Impact of Arnica Montana on Postoperative Pain, Swelling and Trismus Following the Surgical Extraction of Impacted Third Molars: A Split Mouth Randomized Clinical Double Blinded Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
Saint-Joseph University · Academic / Other
Sex
All
Age
16 Years – 40 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGArnica montanaAssess the effect of arnica montana on pain, swelling ans trismus after impacted third molar surgery
OTHERPlaceboPatients will take placebo drug after surgeries

Timeline

Start date
2022-02-03
Primary completion
2023-08-20
Completion
2023-08-20
First posted
2024-01-05
Last updated
2024-01-05

Locations

1 site across 1 country: Lebanon

Source: ClinicalTrials.gov record NCT06193720. Inclusion in this directory is not an endorsement.