Clinical Trials Directory

Trials / Completed

CompletedNCT00363038

Effects of Topical Vitamin K, Vitamin K and Retinol, and Arnica on Post-Laser Bruising

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
16 (actual)
Sponsor
Northwestern University · Academic / Other
Sex
All
Age
20 Years – 60 Years
Healthy volunteers
Accepted

Summary

The objective of this study is to assess the comparative utility of topical formulations in hastening the resolution of skin bruising. For each subject, four standard bruises of 7 mm diameter each were created on the bilateral upper inner arms, 5 cm apart, two per arm, using a 595-nm pulsed-dye laser. Randomization was used to assign one topical agent (5% vitamin K, 1% vitamin K and 0.3% retinol, 20% arnica or white petrolatum) to exactly one bruise per subject, which was then treated under occlusion twice a day for 2 weeks. A dermatologist rated bruises in standardized photographs immediately after bruise creation and at week 2.

Conditions

Interventions

TypeNameDescription
DRUGPetrolatum United States Pharmacopeia (USP)Topical formation applied to bruise twice daily for 2 weeks.
DRUGVitamin K and retinol ointmentTopical formation applied to bruise twice daily for 2 weeks.
DRUGArnica ointmentTopical formation applied to bruise twice daily for 2 weeks.
DRUGVitamin K ointmentTopical formation applied to bruise twice daily for 2 weeks.

Timeline

Start date
2006-07-01
Primary completion
2006-08-01
Completion
2006-08-01
First posted
2006-08-15
Last updated
2021-12-03
Results posted
2012-12-04

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00363038. Inclusion in this directory is not an endorsement.