DRKS00008764
Recruiting
N/A
Characterization of the role of blood circulation and neovascularization in acute and chronic pruritus - iETOP
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- chronic pruritus in patients suffering from prurigoAcute pruritus in itching modelsHealthy volunteers
- Sponsor
- Charité - Universitätsmedizin Berlin
- Enrollment
- 40
- Status
- Recruiting
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Inclusion criteria healthy subjects:
- •The volunteers must be over eighteen, and be able to communicate with the investigator. They must be able to understand the contents of the study and they need to consent to participate in the study. Only male subjects.
- •Inclusion criteria patients:
- •1\. Signed informed consent
- •2\. Prurigo patients with chronic pruritus (\> 6 months) and a severity of prurigo using VAS \= 6/10
- •3\. The patient willing to only use the mentioned products and no other own externa. As rescue medication in severe itching, patients receive a care cream DAC base cream that can be applied as often as desired.
- •4\. Of full age
- •5\. Both male and female patients
Exclusion Criteria
- •Exclusion criteria subjects:
- •Known history of hypersensitivity to any of the substances to be applied.
- •Regular or current intake of medications against itch such as antihistamines, topical or systemic steroids, immunosuppressants or gabapentin.
- •Participation in a clinical trial in the last 30 days.
- •Exclusion criteria patients:
- •1\. Therapeutic UV radiation during the last 6 weeks before the start of the investigation or during the investigation
- •2\. Topical antihistamines, steroids or mast cell stabilizers in the last 3 weeks prior to the study or during the study
- •3\. Systemic medications such antihistamnika, antidepressants, antipsychotics, corticosteroids are permitted if:
- •a) the medication were taken since at least the last 4 weeks prior to the study and
- •b) there has been no changes regarding the use or dosage during the study
Outcomes
Primary Outcomes
Not specified
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