Clinical TrialID 5219

Investigation of the Effect of Vitamin K3-lotion for the Treatment of Cetuximab Induced Folliculitis

NCT01094444

Folliculitis

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Record Fields

Scalar fields from the final clinical_trial record.

Clinical Trial Id
5219
Evidence Id
5219
Core Evidence Id
5219
Source Clinical Trial Id
5201
Herb2 Clinical Trial Id
HBCT005201
Nct Id
NCT01094444
Title
Investigation of the Effect of Vitamin K3-lotion for the Treatment of Cetuximab Induced Folliculitis
Status
Completed
Phase
Phase 2
Study Result
No
Study Condition
Folliculitis
Study Type
Interventional
Study Design
Allocation: NON_RANDOMIZED|Intervention Model: PARALLEL|Masking: TRIPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR)|Primary Purpose: TREATMENT
Intervention
OTHER: Vitamin K3
Intervention Allocation
Non_Randomized
Intervention Model
Parallel
Intervention Mask
Triple
Intervention Purpose
Treatment
Gender
All
Age
Adult, Older_Adult
Enrollment
30
Outcome Measure
Potential reduction in skin toxicity by vitamin K3 lotion, Reduction in numbers of papulo-pustular eruptions in the treatment fields. Changes in follicular eruptions, dryness/redness of skin estimated by CTCAE 4.0. Patients own experience of efficacy estimated by questionaire and VAS scale., 3 months
Sponsor Collaborator
Per Pfeiffer
Funded By
OTHER
Location
Odense University Hospital, Odense C, 5000, Denmark
Other Id
9.15
Start Date
2010-05
Primary Completion Date
2013-12
Completion Date
2014-11
First Posted
2010-03-29
Results First Posted
Last Update Posted
2020-11-16
Study Document
Study Url
https://clinicaltrials.gov/study/NCT01094444
Title Cn
Title En
Investigation of the Effect of Vitamin K3-lotion for the Treatment of Cetuximab Induced Folliculitis
Bilingual Status
semi_complete