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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00442091
Other study ID # 20070010
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date December 2010
Est. completion date December 2019

Study information

Verified date March 2020
Source Odense University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Dandelion juice has been used in herbal medicine for at least 1000 years. Vesicular hand eczema is a rare, but difficult to treat, type of hand eczema. One case report has shown that ingestion of dandelion juice could induce a beneficial effect on this type of eczema. The purpose of this study is to test whether this effect can be retrieved in other patients.


Description:

Dandelion juice has been used in herbal medicine for at least 1000 years. One case report has shown a beneficial effect of this herbal remedy on dyshidrotic hand eczema, and the purpose of this pilot study is to test whether this effect can be retrieved in other patients.

The patients are recruited from our out-patient clinic. Only patients with negative patch tests to Compositae are offered treatment with dandelion juice for 20-30 days.


Recruitment information / eligibility

Status Completed
Enrollment 4
Est. completion date December 2019
Est. primary completion date December 2019
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Adult patients with dyshidrotic eczema for at least 1 year and negative patch test reactions to Compositae (tested within the last 3 years) and normal renal and hepatic blood tests.

Exclusion Criteria:

- Treatment with systemic steroids or other immunosuppressive/-modulating drugs, including UV therapy, within the last 3 months.

- Pregnancy, lactation.

- Compositae contact allergy.

- Liver or gall bladder disease.

- Abnormal renal or hepatic blood tests.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
dandelion juice
10 ml bid for 20-30 days

Locations

Country Name City State
Denmark Department of Dermatology, Odense University Hospital Odense

Sponsors (1)

Lead Sponsor Collaborator
Odense University Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary Improvement in dyshidrotic hand eczema in the study period assessed by HECSI score. 3-4 weeks
Secondary Improvement in dyshidrotic eczema in the study period assessed by the patient (Visual Analog Scale). 3-4 weeks