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
| Type | Name | Description |
|---|---|---|
| DRUG | Petrolatum United States Pharmacopeia (USP) | Topical formation applied to bruise twice daily for 2 weeks. |
| DRUG | Vitamin K and retinol ointment | Topical formation applied to bruise twice daily for 2 weeks. |
| DRUG | Arnica ointment | Topical formation applied to bruise twice daily for 2 weeks. |
| DRUG | Vitamin K ointment | Topical 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.