- Trials with a EudraCT protocol (5)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
5 result(s) found for: Daflon.
Displaying page 1 of 1.
EudraCT Number: 2012-003559-13 | Sponsor Protocol Number: CL3-05682-105 | Start Date*: 2013-05-20 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Clinical non-inferiority study between Daflon 1000 mg, one oral suspension in a sachet per day and Daflon 500 mg, 2 tablets daily after eight weeks of treatment in patients suffering from symptomat... | |||||||||||||
Medical condition: Patients suffering from symptomatic Chronic Venous Disease (CVD). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SI (Completed) CZ (Completed) ES (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021270-11 | Sponsor Protocol Number: CL2-05682-102 | Start Date*: 2010-09-30 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Impact of Daflon 500 mg on the progression of chronic venous disease and symptoms in patients operated on for varicose veins with conservation of the great saphenous vein. A multicentre, double bl... | |||||||||||||
Medical condition: Patients suffering from chronic venous disease and for whom ASVAL (Ambulatory Selective Varicose veins Ablation Local anesthesia) surgery is indicated. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001947-23 | Sponsor Protocol Number: PEL01CVH | Start Date*: 2007-11-28 | |||||||||||
Sponsor Name:HELP Pharmaceuticals S.A. | |||||||||||||
Full Title: A multicenter, randomized, parallel patients’ group, comparative clinical trial for the assessement of efficacy and safety of Pelethrocin®/HELP 500 mg (generic diosmin & hesperidin MPFF) versus Daf... | |||||||||||||
Medical condition: Chronic Venous Insufficiency | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001916-44 | Sponsor Protocol Number: MiFlaPRO_2019 | Start Date*: 2020-01-28 |
Sponsor Name:Medical University Innsbruck, Department of Visceral, Transplant und Thoracic Surgery | ||
Full Title: A multicenter, randomized, double blind placebo controlled trial of Micronized purified Flavonoid- Fraction (MPFF) in the management of radiation proctitis | ||
Medical condition: Patients with radiation proctitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003633-28 | Sponsor Protocol Number: CL3-05682-109 | Start Date*: 2018-05-02 | |||||||||||
Sponsor Name:Institut de Recherches Internationales SERVIER (I.R.I.S.) | |||||||||||||
Full Title: Clinical non-inferiority study between Micronized purified flavonoid fraction 1000 mg, one chewable tablet per day and Micronized Purified Flavonoid Fraction 500 mg, 2 tablets daily after eight ... | |||||||||||||
Medical condition: symptomatic Chronic Venous Disease (CVD). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) AT (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
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