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Comparison Study With E-DO in Chronic Hand Dermatitis

NCT00556855 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 67

Last updated 2009-01-12

No results posted yet for this study

Summary

The objective of this study is to evaluate the topical E-DO in patients with Chronic Hand Dermatitis (fu kuei shou).

Conditions

  • Chronic Hand Dermatitis

Interventions

OTHER

E-DO

topical lotion, once daily (evening), total duration: 4 weeks

OTHER

Placebo

topical lotion, once daily (evening), total duration: 4 weeks

Sponsors & Collaborators

  • HenKan Pharmaceutical Co., Ltd.

    lead INDUSTRY

Principal Investigators

  • Chia-Yu Chu, MD, PhD · Department of Dermatology, Nation Taiwan University Hopital, R.O.C.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-12-31
Primary Completion
2008-07-31
Completion
2008-07-31

Countries

  • Taiwan

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00556855 on ClinicalTrials.gov