Efficacy of Arnica Montana in Reducing Postoperative Edema and Pain
NCT03944629 · Status: COMPLETED · Type: INTERVENTIONAL · Enrollment: 53
Last updated 2026-01-29
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).
Conditions
- Arnica
- Third Molar Extraction
Interventions
- DRUG
-
SinEcch
The study group will be comprised of subjects who will receive homeopathic Arnica montana (SinEcch™) for perioperative management of edema and pain.
- OTHER
-
Placebo
The control group will be comprised of subjects who will receive matching SinEcch™ placebo (sugar pill).
Sponsors & Collaborators
-
Tufts University
lead OTHER
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 40 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2018-01-26
- Primary Completion
- 2022-06-14
- Completion
- 2022-06-14
Countries
- United States
Study Locations
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