- Trials with a EudraCT protocol (3)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3 result(s) found for: Heavy legs.
Displaying page 1 of 1.
| EudraCT Number: 2017-004804-23 | Sponsor Protocol Number: KCT13/2017–FLEBAVEN/SI | Start Date*: 2018-06-15 | |||||||||||
| Sponsor Name:Krka, d.d., Novo mesto | |||||||||||||
| Full Title: The efficacy and safety of a single dose Flebavena® (Diosmin) of 1000 mg per day in patients with chronic venous disease (LIGHTEN-UP) | |||||||||||||
| Medical condition: Patients diagnosed with primary chronic vein disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SI (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-013391-44 | Sponsor Protocol Number: EDX09/01 | Start Date*: 2010-02-05 | |||||||||||
| Sponsor Name:OM PHARMA SA | |||||||||||||
| Full Title: Multicentre, double blind, placebo-controlled, randomised clinical study to assess the efficacy and safety of Doxium® 500 three times daily in patients suffering from chronic venous insufficiency (... | |||||||||||||
| Medical condition: Chronic Venous Insufficiency (CVI) CEAP Class C3 or C4 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) PT (Completed) PL (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-005003-40 | Sponsor Protocol Number: BTS651/12 | Start Date*: 2013-01-21 |
| Sponsor Name:MUCOS Pharma GmbH & Co. KG | ||
| Full Title: Effects of Wobenzym® plus in healthy, sportive people after eccentric exercise - a randomized, two-stage, double-blind, placebo-controlled cross-over trial | ||
| Medical condition: "Healthy volunteers" Influence of the product on exercise induced muscle damage, noticable in temporal strength loss and muscle soreness. The indication is as defined in the SmPC: Swelling and infl... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
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Query did not match any studies.