- Trials with a EudraCT protocol (80)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
80 result(s) found for: Foot pressure.
Displaying page 1 of 4.
EudraCT Number: 2009-014276-22 | Sponsor Protocol Number: 06FB/DE02 | Start Date*: 2010-02-19 | |||||||||||
Sponsor Name:Laboratoires Genevrier | |||||||||||||
Full Title: Prospective, randomised, multi-centre, blind-observer, controlled, parallel-group study comparing the efficacy and the safety of DERMAGEN® versus conventionnal treatment in the treatment of diabeti... | |||||||||||||
Medical condition: Diabetic neuropathic foot ulcer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003636-38 | Sponsor Protocol Number: SBG-1-13 | Start Date*: 2008-09-22 | |||||||||||
Sponsor Name:Biotec Pharmacon ASA | |||||||||||||
Full Title: Estudio aleatorizado, doble ciego, controlado con placebo para evaluar la eficacia y seguridad de beta-1,3/1,6- glucano soluble (SBG) en úlceras crónicas del pie en pacientes con diabetes. A random... | |||||||||||||
Medical condition: Úlceras crónicas del pie en pacientes con diabetes Chronic foot ulcers in patients with diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001653-27 | Sponsor Protocol Number: MarsyasII | Start Date*: 2019-12-20 | |||||||||||
Sponsor Name:Aposcience AG | |||||||||||||
Full Title: A randomized, placebo-controlled, double-blind study to evaluate safety and dose dependent clinical efficacy of APO-2 at three different doses in patients with diabetic foot ulcer (MARSYAS II) | |||||||||||||
Medical condition: Diabetic Foot Ulcer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) CZ (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005916-15 | Sponsor Protocol Number: MC-UK.3/AVK | Start Date*: 2008-04-25 | |||||||||||
Sponsor Name:medac Gesellschaft für klinische Spezialpräparate mbH | |||||||||||||
Full Title: Low dose Urokinase therapy by patients with diabetic foot syndrom and critical limb ischemia versus conventionel standard therapy. A randomised, open, controlled Phase III-study. | |||||||||||||
Medical condition: Patients with angiopathic or angioaneuropathic diabetic foot syndrome and critical limb ischemia without the possibility of surgical or interventional revascularisation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005784-10 | Sponsor Protocol Number: A6301083 | Start Date*: 2007-12-21 | |||||||||||
Sponsor Name:Pfizer Inc, 235 East 42nd Street, New York, NY 10017 | |||||||||||||
Full Title: A 6 MONTH, PROSPECTIVE, RANDOMIZED, DOUBLE BLIND, PLACEBO-CONTROLLED, PARALLEL GROUP, MULTIPLE CENTER TRIAL TO EVALUATE THE EFFICACY AND SAFETY OF FRAGMIN IN THE TREATMENT OF CHRONIC NEUROISCHAEMIC... | |||||||||||||
Medical condition: Diabetic Foot Ulcer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) NL (Completed) GB (Prematurely Ended) DK (Prematurely Ended) LT (Prematurely Ended) FI (Prematurely Ended) FR (Completed) ES (Completed) GR (Completed) CZ (Completed) AT (Completed) BE (Completed) IT (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005580-16 | Sponsor Protocol Number: REDDSTAR-01 | Start Date*: 2016-08-03 | |||||||||||
Sponsor Name:Steno Diabetes Center A/S | |||||||||||||
Full Title: A Phase 1b, open label, uncontrolled non-randomised single dose study to examine the safety of topically applied bone marrow derived allogeneic mesenchymal stromal cells (REDDSTAR ORBCEL-M) seeded ... | |||||||||||||
Medical condition: Patients with non-healing neuroischaemic diabetic foot wounds | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020437-12 | Sponsor Protocol Number: DT-DP-D2b | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:DermaTools Biotech GmbH | |||||||||||||
Full Title: A multicentric, double blind, randomized, comparative Phase II b study of the efficacy of a wound healing solution in patients with diabetic foot ulcer | |||||||||||||
Medical condition: diabetic foot ulcer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) LV (Prematurely Ended) LT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004787-74 | Sponsor Protocol Number: Final protocol | Start Date*: 2005-04-19 |
Sponsor Name:Royal Group of Hospitals Trust | ||
Full Title: A double blind, prospective, randomised, controlled clinical trial to evaluate the effect of topical phenytoin, on healing, in diabetic foot ulcers. | ||
Medical condition: Diabetes Mellitus and associated diabetic foot ulceration | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-011755-47 | Sponsor Protocol Number: 2007-001 | Start Date*: 2009-07-06 |
Sponsor Name:Vivostat A/S | ||
Full Title: A feasibility study to evaluate the effect of Vivostat® Platelet Rich Fibrin (PRF®) in the treatment of diabetic foot ulcers | ||
Medical condition: - Diabetic foot ulcers Texas Grade I placed at or below the anchle -Non-ischaemic, non-infected ulcers | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003594-17 | Sponsor Protocol Number: NL59077.018.16 | Start Date*: 2018-05-28 | |||||||||||
Sponsor Name:AMC | |||||||||||||
Full Title: Effects of a single denosumab injection on reduction of total contact cast treatment and consolidation of bonefractures caused by acute Charcotfoot in patients with diabetes mellitus (CHARCOT st... | |||||||||||||
Medical condition: charcot foot | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005841-19 | Sponsor Protocol Number: DT-DP-D3 | Start Date*: 2013-10-10 | |||||||||||
Sponsor Name:DermaTools Biotech GmbH | |||||||||||||
Full Title: A Multicentric, Double Blind, randomised, Comparative Phase III Study of the Efficacy of the new Wound Healing Solution Diperoxochloric acid (DPOCL, DermaPro®) compared to isotonic Sodium Chloride ... | |||||||||||||
Medical condition: Diabetic foot ulcers with mean diameter between 1.5 and 5 cm after débridement (if indicated); wound stage Wagner grade I or II, Armstrong stadium A or C (for Wagner-Armstrong-Classification), trea... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) LV (Completed) LT (Completed) HU (Completed) PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004782-11 | Sponsor Protocol Number: 2002C014G | Start Date*: 2017-12-05 | |||||||||||
Sponsor Name:Prometic Biotherapeutics Ltd | |||||||||||||
Full Title: A Phase 1/2A Prospective, Dose-Escalation, Open-Label Study of the Safety, Feasibility, and Initial Efficacy of Subcutaneous Plasminogen (Human) 10 for the Treatment of Diabetic Foot Ulcer | |||||||||||||
Medical condition: Diabetic foot ulcer (DFU) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-021015-16 | Sponsor Protocol Number: TFM-CL3-002 | Start Date*: 2010-09-30 | |||||||||||
Sponsor Name:Olympus France SAS | |||||||||||||
Full Title: A Phase III, Double-Blind, Placebo Controlled, Parallel Group, International, Multicenter Study of 12 Weeks Treatment with Trafermin 0.01% Spray in Patients with Diabetic Foot Ulcer of Neuropathic ... | |||||||||||||
Medical condition: Wound closure rate of diabetic foot ulcers (DFUs) of neuropathic origin. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) BE (Completed) DK (Completed) SE (Completed) DE (Completed) NL (Completed) HU (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006754-26 | Sponsor Protocol Number: PLA/01/06 | Start Date*: 2006-11-28 | |||||||||||
Sponsor Name:MASTELLI SRL | |||||||||||||
Full Title: DIABETIC FOOT ULCERS AND POLYDEOXYRIBONUCLEOTIDE (PLACENTEX INTEGRO MASTELLI) AS A TREATMENT FOR WOUND HEALING | |||||||||||||
Medical condition: Diabetic foot ulcer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) SI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021014-33 | Sponsor Protocol Number: TFM-CL3-001 | Start Date*: 2010-09-30 | |||||||||||
Sponsor Name:Olympus France SAS | |||||||||||||
Full Title: A Phase III, Double-Blind, Placebo Controlled, Parallel Group, International, Multicenter Study of 12 Weeks Treatment with Trafermin 0.01% Spray in Patients with Diabetic Foot Ulcer of Neuropathic ... | |||||||||||||
Medical condition: Wound closure rate of diabetic foot ulcers (DFUs) of neuropathic origin. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001392-32 | Sponsor Protocol Number: SC-VLU-001 | Start Date*: 2021-11-10 | ||||||||||||||||
Sponsor Name:SolasCure Ltd | ||||||||||||||||||
Full Title: An adaptive open label, multiple ascending dose study of the safety, tolerability and bio-effect of Aurase for wound debridement in patients with venous leg ulcers and diabetic foot ulcers (CLEANVL... | ||||||||||||||||||
Medical condition: Venous Leg Ulcer Diabetic Foot Ulcer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-000091-40 | Sponsor Protocol Number: RS03-2004 | Start Date*: 2005-11-08 | |||||||||||
Sponsor Name:ApoPharma Inc. | |||||||||||||
Full Title: Pivotal Study to Evaluate the Efficacy and Safety of Dermal - Living Skin Replacement (Dermal – LSR) in the Treatment of Chronic Diabetic Foot Ulcers | |||||||||||||
Medical condition: Chronic Diabetic Foot Ulcers | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001397-15 | Sponsor Protocol Number: BMMNC_CLI_001 | Start Date*: 2016-06-15 | |||||||||||
Sponsor Name:Institut klinické a experimentální medicíny | |||||||||||||
Full Title: A prospective, randomized study to compare the effect on tissue oxygenation and clinical outcome of autologous bone marrow-derived mononuclear cell therapy with standard treatment in patients with ... | |||||||||||||
Medical condition: Autologous cell therapy (ACT) is new technique for patients with critical limb ischemia and diabetic foot (DF). In our study, the effect of ACT and also the repetitive treatment will be compared wi... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004527-67 | Sponsor Protocol Number: DT-DP-DFU-CR-04 | Start Date*: 2018-08-06 |
Sponsor Name:DermaTools Biotech GmbH | ||
Full Title: A Randomised Dose Finding Study Comparing The Safety And Efficacy Of three blinded doses of Diperoxochloric Acid (DPOCl, DermaPro®) and A Standard Moist Wound Dressing In Patients With Non-Healing... | ||
Medical condition: Diabetic foot ulcer with mean diameter between 1.5 and 4 cm after débridement if indicated), Wound stage Wagner grade I or II, Armstrong stadium A or C (for Wagner-Armstrong-Classification), tr... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: LV (Completed) EE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000692-15 | Sponsor Protocol Number: 05-DFU-001 | Start Date*: 2006-05-03 |
Sponsor Name:Intercytex | ||
Full Title: A prospective single centre, open label, pilot study to evaluate the safety of ICXP007 plus standard of care, for the treatment of lower extremity chronic, neuropathic diabetic foot ulcers | ||
Medical condition: Diabetic foot ulcers | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
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