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NCT01164644 · ClinicalTrials.gov registry record · NA
The Utility of Peri-operative Arnica Montana for Reduction of Ecchymosis in Rhinoplasty Surgery
A NA study of Ecchymosis, sponsored by University of Wisconsin, Madison.
- Completed
- Registry status
- NA
- Development phase
- 28
- Enrollment target
- 1
- Study location
NCT01164644 is a NA study of Ecchymosis that has completed, run by University of Wisconsin, Madison. The registered enrollment target is 28 participants. The trial reports 1 study location across 1 state.
The verdict
NCT01164644, a NA study of Ecchymosis, has completed, sponsored by University of Wisconsin, Madison.
- COMPLETED
- Registry status
- NA
- Development phase
- 28 participants
- Enrollment target
- 1
- Study location
Study Summary
Arnica montana is a homeopathic drug that is made in accordance with the official methods of the Homeopathic Pharmacopoeia of the United States (HPUS) and is commonly used by cosmetic surgeons throughout the world, although there is no study proving its benefit after rhinoplasty surgery. The purpose of the research is to see if Arnica montana will reduce the amount of bruising and the intensity of the bruising after surgery. Photographs of the subject's face will be taken and used to analyze bruising after rhinoplasty surgery in subjects who receive Arnica montana and compare them to photographs of subjects who take a placebo (sugar pill).
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Arnica montana
Study Locations (1)
Wisconsin
- University of Wisconsin-Madison - Madison
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 28 participants |
| Start Date | 2010-06 |
| Est. Completion | 2012-12 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01164644
The ClinicalTrials.gov registry entry for NCT01164644 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 28 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Wisconsin, Madison, which has 1,039 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Ecchymosis appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT01164644 reports 1 study location spanning 1 distinct geographic area - top geographies include Wisconsin.
Frequently Asked Questions
What is clinical trial NCT01164644 about?
NCT01164644 is a clinical study titled "The Utility of Peri-operative Arnica Montana for Reduction of Ecchymosis in Rhinoplasty Surgery". Arnica montana is a homeopathic drug that is made in accordance with the official methods of the Homeopathic Pharmacopoeia of the United States (HPUS) and is commonly used by cosmetic surgeons throughout the world, although there is no study proving its benefit after rhinoplasty surgery. The purpose...
What is the current status of trial NCT01164644?
This trial is currently completed. It is a NA study. The enrollment target is 28 participants. The study started on 2010-06. Estimated completion is 2012-12.
What conditions does trial NCT01164644 study?
This clinical trial studies the following conditions: Ecchymosis.
What interventions are being tested in trial NCT01164644?
The interventions under investigation include: Placebo (DRUG), Arnica montana (DRUG).
Who is sponsoring clinical trial NCT01164644?
This trial is sponsored by University of Wisconsin, Madison, which has 1,039 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01164644 being conducted?
This trial has 1 study location across Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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