- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
8 result(s) found for: Great saphenous vein.
Displaying page 1 of 1.
| EudraCT Number: 2014-003341-10 | Sponsor Protocol Number: NL47979.091.14 | Start Date*: 2018-01-16 |
| Sponsor Name:Rijnstate | ||
| Full Title: Registry of the treatment of primay insufficiency of the great saphenous vein with a diameter >/= 12 mm, anterolateral branches, or great saphenous vein insufficiency below the knee with mechano-... | ||
| Medical condition: varicose veins of the infragenual great saphenous vein, large supragenual great saphenous vein (>= 12 mm) and antero-lateral branch varicose veins | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-004347-37 | Sponsor Protocol Number: VSV2016b | Start Date*: 2017-01-31 |
| Sponsor Name:Helsinki University Hospital | ||
| Full Title: Femoralblock in endovenous laser | ||
| Medical condition: venous disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| 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: 2009-014681-25 | Sponsor Protocol Number: DC 0982 GE 203 1B | Start Date*: 2009-10-21 |
| Sponsor Name:PIERRE FABRE MEDICAMENT-IRPF-IDPF | ||
| Full Title: Pharmacodynamic and clinical assessment of DC 982 GE (2,4 or 6 capsules per day) in patients with chronic venous disorders : randomised, placebo-controlled, dose effect, double blind, parallel gro... | ||
| Medical condition: Treatment of venous lymphatic insufficiency symptoms related to chronic venous disorders. | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: FR (Completed) EE (Completed) LT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-005574-39 | Sponsor Protocol Number: Surgery&TumescenceV3 | Start Date*: 2011-12-21 |
| Sponsor Name:Hull and East Yorkshire Hospitals NHS Trust | ||
| Full Title: A Randomised Controlled Trial of Tumescent Anaesthesia in addition to Surgical Ligation and Stripping of the Great Saphenous Vein | ||
| Medical condition: Superficial Venous Insufficiency | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-000967-10 | Sponsor Protocol Number: RC31/14/7441 | Start Date*: 2019-05-24 |
| Sponsor Name:University Hospital Toulouse | ||
| Full Title: Autologous transplantation of Adipose tissue derived mesenchymal Stroma/stem Cells (ASC) in patients with critical limb ischemia: a phase II study (ACellDream 2). | ||
| Medical condition: Patients with rest pain or ischemic ulcers/gangrene of the lower limb and without option for revascularization or poor option. Or patients with with rest pain or ischemic ulcers and persistent CL... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-005575-16 | Sponsor Protocol Number: BufferedTumescenceV3 | Start Date*: 2011-12-21 |
| Sponsor Name:Hull & East Yorkshire Hospitals NHS Trust | ||
| Full Title: Tumescent Anaesthesia in Endovenous Laser Ablation of Varicose Veins: A Randomised Controlled Trial of a Buffered Tumescent Solution | ||
| Medical condition: Pain of injection of a tumescent anaesthetic solution used during EndoVenous Laser Ablation of Varicose Veins. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-010062-33 | Sponsor Protocol Number: ABH-DERMAGRAFT-001-08 | Start Date*: 2009-09-24 | |||||||||||
| Sponsor Name:Advanced BioHealing Inc | |||||||||||||
| Full Title: A Prospective, Multi-center, Randomized, Controlled Clinical Investigation of Dermagraft® in Subjects with Venous Leg Ulcers | |||||||||||||
| Medical condition: Venous leg ulcers | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) SE (Completed) GB (Completed) EE (Completed) AT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
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