Stopped: The study could not be conducted since funding was not obtained.
The purpose of this study is to assess the perioperative use of Arnica Montana and the combined use of Arnica Montana and Bromelain in aiding the body's wound healing functions during the postoperative period after rhinoplasty. The secondary objective of the study is to determine if there is a reduction in postoperative edema when Arnica Montana and Bromelain are combined. Another secondary objective is to demonstrate increased patient satisfaction with the use of Arnica Montana and the combination Arnica Montana and Bromelain.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Ecchymosis extent 7 days post rhinoplasty
Timeframe: 7 days
Ecchymosis extent 14 days post rhinoplasty
Timeframe: 14 days
Ecchymosis extent 28 days post rhinoplasty
Timeframe: 28 days
Ecchymosis color density 7 days post rhinoplasty
Timeframe: 7 days
Ecchymosis color density 14 days post rhinoplasty
Timeframe: 14 days
Ecchymosis color density 28 days post rhinoplasty
Timeframe: 28 days
Edema 7 days post rhinoplasty
Timeframe: 7 days
Edema 14 days post rhinoplasty
Timeframe: 14 days
Edema 28 days post rhinoplasty
Timeframe: 28 days