Dandelion Juice in the Treatment of Dyshidrotic Hand Eczema
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ClinicalTrials.gov Identifier: NCT00442091 |
Recruitment Status :
Completed
First Posted : March 1, 2007
Last Update Posted : March 4, 2020
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Vesicular Palmoplantar Eczema Pompholyx | Drug: dandelion juice | Not Applicable |
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.
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 4 participants |
Allocation: | N/A |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | Dandelion Juice in the Treatment of Dyshidrotic Hand Eczema |
Study Start Date : | December 2010 |
Actual Primary Completion Date : | December 2019 |
Actual Study Completion Date : | December 2019 |

Arm | Intervention/treatment |
---|---|
10 ml of dandelion juice twice daily |
Drug: dandelion juice
10 ml bid for 20-30 days |
- Improvement in dyshidrotic hand eczema in the study period assessed by HECSI score. [ Time Frame: 3-4 weeks ]
- Improvement in dyshidrotic eczema in the study period assessed by the patient (Visual Analog Scale). [ Time Frame: 3-4 weeks ]

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Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
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.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00442091
Denmark | |
Department of Dermatology, Odense University Hospital | |
Odense, Denmark, DK-5000 |
Principal Investigator: | Evy Paulsen, Dr. | Department of Dermatology, Odense University Hospital, DK-5000 Odense C |
Responsible Party: | Evy Paulsen, Consultant dermatologist, Ph.D., Odense University Hospital |
ClinicalTrials.gov Identifier: | NCT00442091 |
Other Study ID Numbers: |
20070010 |
First Posted: | March 1, 2007 Key Record Dates |
Last Update Posted: | March 4, 2020 |
Last Verified: | March 2020 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
Dandelion herbal remedy hand eczema Compositae |
Eczema Eczema, Dyshidrotic Dermatitis |
Skin Diseases Skin Diseases, Eczematous Skin Diseases, Vesiculobullous |