Clinical Trials Directory

Trials / Completed

CompletedNCT03944629

Efficacy of Arnica Montana in Reducing Postoperative Edema and Pain

Efficacy of Arnica Montana in Reducing Postoperative Edema and Pain Following Third Molar Extraction

Status
Completed
Phase
Study type
Interventional
Enrollment
53 (actual)
Sponsor
Tufts University · Academic / Other
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Accepted

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).

Detailed description

Our study aims to look at the efficacy of homeopathic Arnica montana (SinEcch™) in reducing postoperative edema and pain. Pain will be measured using the visual analog scale (VAS). Swelling will be measured using a 3D imaging system. This is the first study using the 3D imaging system that looks at the effect of homeopathic Arnica montana in reducing facial swelling following the surgical removal of impacted third molars. Although SinEcch is marketed mainly for management of postoperative swelling and bruising, Arnica Montana has been used for managing the sequelae of postoperative inflammation including pain so one of the secondary outcome measure for this study is to measure the efficacy of SinEcch in management of post-operative pain.

Conditions

Interventions

TypeNameDescription
DRUGSinEcchThe study group will be comprised of subjects who will receive homeopathic Arnica montana (SinEcch™) for perioperative management of edema and pain.
OTHERPlaceboThe control group will be comprised of subjects who will receive matching SinEcch™ placebo (sugar pill).

Timeline

Start date
2018-01-26
Primary completion
2022-06-14
Completion
2022-06-14
First posted
2019-05-09
Last updated
2026-01-29
Results posted
2026-01-29

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03944629. Inclusion in this directory is not an endorsement.