- Trials with a EudraCT protocol (3)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
3 result(s) found for: Hypericin.
Displaying page 1 of 1.
| EudraCT Number: 2011-001819-30 | Sponsor Protocol Number: Sano2011 | Start Date*: 2011-10-18 | |||||||||||
| Sponsor Name:Sanochemia Pharmazeutika AG | |||||||||||||
| Full Title: Detection of non-muscle invasive bladder cancer using PVP-Hypericin (VidonĀ®) fluorescence cystoscopy (Hypericin PDD) | |||||||||||||
| Medical condition: Suspected non-muscle invasive (superficial) bladder cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-001302-25 | Sponsor Protocol Number: 2008-0312-08 | Start Date*: 2009-11-05 | |||||||||||
| Sponsor Name:Lab for pharmaceutical biology [...] | |||||||||||||
| Full Title: Evaluation of the benefits and effects of hypericin Photodynamic therapy (PDT) in the clinical treatment of superficial bladder carcinoma. | |||||||||||||
| Medical condition: the study population consists of 10 patients with anatomopathologically proven muscle invasive TCC without metastasis. These patients require a cystoscopy. Before the planned cystoscopy, the bladde... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-004004-20 | Sponsor Protocol Number: UI04/6748 | Start Date*: 2005-09-26 |
| Sponsor Name:University of Leeds | ||
| Full Title: A Randomised, Double-blind, Placebo Controlled trial to test the efficacy of St John's Wort (Hypericum Perforatum) for Premenstrual Syndrome. | ||
| Medical condition: The 'premenstrual syndrome' is a cyclical condition occurring 7-10 days before the onset of menstruation, and is relieved at, or shortly after commencement of menstrual flow. The most commonly repo... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
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