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Efficacy of Arnica D1 Ointment After Upper Blepharoplasty

Efficacy of Arnica D1 Ointment After Upper Blepharoplasty: a Randomized, Double-blind Placebo-controlled Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01598909
Acronym
ARINE
Enrollment
136
Registered
2012-05-15
Start date
2013-01-31
Completion date
2014-01-31
Last updated
2015-08-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blepharoplasty, Upper Eyelid Blepharoplasty

Keywords

blepharoplasty, arnica, homeopathy

Brief summary

Arnica ointment is currently used in homeopathic preparations for strains and bruises. In the field of plastic surgery, some surgeons advise patients undergoing blepharoplasty to use Arnica in order to prevent postoperative ecchymosis, swelling and pain. Thus far, no decent study evaluated the efficacy of topical Arnica ointment in reducing ecchymosis or surgical outcome after upper blepharoplasty. We hypothesize that application of Arnica ointment postoperatively will reduce the development of ecchymosis and improve outcome.

Interventions

DRUGArnica

Application of Arnica ointment periorbitally

Application of Arnica ointment, twice a day, for the period of one week.

Sponsors

Wynand BWH Melenhorst, MD
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients undergoing primary blepharoplasty

Exclusion criteria

* use of anticoagulants

Design outcomes

Primary

MeasureTime frameDescription
Surgical outcome7 days and 6 weeks postoperativelyOverall judgment of surgical outcome, based on the combined analysis of the amount of ecchymosis, swelling and redness, by an unrelated, uninvolved and blinded plastic surgeon.

Secondary

MeasureTime frame
amount of tissue swelling; redness; pain; postoperative recovery; patient satisfaction3, 7 and 42 days postoperatively

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026