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The effect of topical vitamin K on skin rash

Phase 3
Recruiting
Conditions
Skin rash.
Rash and other nonspecific skin eruption
Registration Number
IRCT20150304021338N3
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
48
Inclusion Criteria

Patients with metastatic colorectal cancer that are candidates for treatment with Cetuximab .
Patients with grade 1 to 4 skin lesions, after using Cetuximab(based on Common Terminology Criteria for Adverse Events4 (CTCAE4))
Be over 18 years old
The patient should not undergo radiotherapy.
Have a desire to participate in the study.

Exclusion Criteria

The patient has skin lesions before receiving cetuximab (including rash, acne, pustules, inflammatory erythema)
Being pregnant or in breastfeeding duration
Previous history of allergies to compounds containing vitamin K
Has a psychiatric disorder that is not able to participate in the study
For other reasons, he is taking drugs that have a drug interaction with topical vitamin K
Be taking medicinal compounds containing vitamin K

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Grade of skin lesions, based on Common Terminology Criteria for Adverse Events4 (CTCAE4). Timepoint: At the beginning of the study and 4 and 8 weeks after using topical vitamin K. Method of measurement: Based on CTCEA4.
Secondary Outcome Measures
NameTimeMethod
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