Clinical TrialID 866

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

NCT00363038

Ecchymosis

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
866
Evidence Id
866
Core Evidence Id
866
Source Clinical Trial Id
848
Herb2 Clinical Trial Id
HBCT000848
Nct Id
NCT00363038
Title
Effects of Topical Vitamin K, Vitamin K and Retinol, and Arnica on Post-Laser Bruising
Status
Completed
Phase
Study Result
Yes
Study Condition
Ecchymosis
Study Type
Interventional
Study Design
Allocation: RANDOMIZED|Intervention Model: SINGLE_GROUP|Masking: DOUBLE (PARTICIPANT, INVESTIGATOR)|Primary Purpose: TREATMENT
Intervention
DRUG: Petrolatum United States Pharmacopeia (USP)|DRUG: Vitamin K and retinol ointment|DRUG: Arnica ointment|DRUG: Vitamin K ointment
Intervention Allocation
Randomized
Intervention Model
Single_Group
Intervention Mask
Double
Intervention Purpose
Treatment
Gender
All
Age
Adult
Enrollment
16
Outcome Measure
Average Bruise Change, Mean change in bruising level detected by dermatologist rater on Visual Analogue Scale at 2 weeks compared with baseline for each of the four agents (Petrolatum USP, Vitamin K and retinol ointment, Vitamin K ointment, Arnica ointment). When responding to a VAS item, respondents specify the bruise severity by indicating a position along a continuous line between two end-points (0 and 10, 10 being the most bruised)., Baseline and 2 weeks
Sponsor Collaborator
Northwestern University
Funded By
OTHER
Location
Northwestern University Feinberg School of Medicine, Department of Dermatology, Chicago, Illinois, 60611, United States
Other Id
1253-015
Start Date
2006-07
Primary Completion Date
2006-08
Completion Date
2006-08
First Posted
2006-08-15
Results First Posted
2012-12-04
Last Update Posted
2021-12-03
Study Document
Study Url
https://clinicaltrials.gov/study/NCT00363038
Title Cn
Title En
Effects of Topical Vitamin K, Vitamin K and Retinol, and Arnica on Post-Laser Bruising
Bilingual Status
semi_complete