Carcinoma, Squamous Cell Clinical Trial
Official title:
Acitretin Plasma Levels Under Hemodialysis
| Verified date | July 2018 |
| Source | University of Zurich |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
Acitretin is given to hemodialysis patients who have developed in-situ or invasive squamous cell carcinoma of the skin in increasing doses up to 25 mg daily for one year.
| Status | Withdrawn |
| Enrollment | 0 |
| Est. completion date | June 2018 |
| Est. primary completion date | December 2014 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
Inclusion criteria: - Hemodialyis patients with at least one case of in-situ or invasive squamous cell carcinoma of the skin Exclusion criteria: - Hepatopathy - Pregnancy |
| Country | Name | City | State |
|---|---|---|---|
| Switzerland | Clinic for Dermatology University Hospital of Zurich | Zurich |
| Lead Sponsor | Collaborator |
|---|---|
| Günther Hofbauer | University of Zurich |
Switzerland,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Plasma levels acitretin | 2009 |
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