- Trials with a EudraCT protocol (15)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
15 result(s) found for: Below Knee Amputation.
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EudraCT Number: 2006-005667-26 | Sponsor Protocol Number: 130256 | Start Date*: 2007-07-11 | ||||||||||||||||
Sponsor Name:Ninewells Hospital | ||||||||||||||||||
Full Title: A randomised, placebo controlled trial of levobupivacaine or the combination of levobupivacaine and clonidine when administered as a sciatic perineural infusion for the prevention of phantom limb p... | ||||||||||||||||||
Medical condition: Pain after amputation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000875-33 | Sponsor Protocol Number: PLATA | Start Date*: 2013-08-27 | |||||||||||
Sponsor Name:Academic Medical Center, University of Amsterdam | |||||||||||||
Full Title: Prevention of Phantom Limb Pain After Transtibial Amputation (PLATA) - Randomized, double-blind, controlled, multi-center trial comparing Optimized intravenous pain control vs Optimized intravenous... | |||||||||||||
Medical condition: Phantom limb pain following amputation of the lower leg due to critical limb ischemia. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) ES (Ongoing) AT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001701-97 | Sponsor Protocol Number: version 2.0, dated 27/04/04 | Start Date*: 2005-12-20 |
Sponsor Name:Royal Berkshire and Battle Hospitals NHS Trust | ||
Full Title: Prospective randomised controlled trial of: MRSA Prophylaxis for lower limb amputation | ||
Medical condition: Post-operative MRSA infection following lower limb amputation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-003637-41 | Sponsor Protocol Number: BIOEU001.00 | Start Date*: 2005-10-26 |
Sponsor Name:Biopure Corporation | ||
Full Title: A Phase II, Multi-Center, Single-Blinded, Placebo-Controlled Study to Evaluate the Safety and Feasibility of Hemoglobin-Based Oxygen Carrier-201 (HBOC-201, hemoglobin-glutamer-250 (bovine)]) on Wo... | ||
Medical condition: Wound Healing in Patients with Peripheral Vascular Disease and Who are Undergoing a Lower Limb Amputation due to Critical Lower Limb Ischemia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000822-58 | Sponsor Protocol Number: C9253 | Start Date*: 2004-07-13 | |||||||||||
Sponsor Name:Sanofi-Synthelabo Groupe | |||||||||||||
Full Title: A double blind randomized study of Clopidogrel 75 mg/d versus placebo on a background of ASA 75-100 mg/d, in peripheral disease (PAD) patient receiving a unilateral below knee by-pass graft. | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) FI (Completed) HU (Completed) IT (Completed) GB (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000240-34 | Sponsor Protocol Number: REX-001-004 | Start Date*: 2016-07-07 | |||||||||||||||||||||
Sponsor Name:Rexgenero Limited | |||||||||||||||||||||||
Full Title: The Efficacy and Safety of Intra-Arterial Administration of Rexmyelocel T to treat Critical Limb Ischemia in Subjects with Diabetes Mellitus: A Multicenter, Randomized, Double-Blind, Placebo Contro... | |||||||||||||||||||||||
Medical condition: Critical Limb Ischemia in patients with Diabetes Mellitus | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Restarted) AT (Completed) NL (Ongoing) HU (Ongoing) PL (Temporarily Halted) PT (Ongoing) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000864-41 | Sponsor Protocol Number: CHUB-patch-lidocaine | Start Date*: 2016-06-02 |
Sponsor Name:Centre Hospitalier Universitaire Brugmann | ||
Full Title: A randomized controlled trial of lidocaine patch for lower limb amputation pain. | ||
Medical condition: Lower limb amputation pain: phantom limb pain and primary/secondary scar hyperalgesia. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-002086-54 | Sponsor Protocol Number: NTR5685 | Start Date*: 2018-09-03 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: A randomized trial of the effect of antiplatelet therapy (Aspirin, Aspirin and Clopidogrel or Ticagrelor) on the occurrence of atherothrombotic and cardiovascular adverse events following lower ext... | ||
Medical condition: It is known that the atherothrombotic cardiovascular adverse event rate in patients with peripheral artery disease (PAD) is high. Also patency rates after (endo)vascular interventions in PAD patien... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006611-29 | Sponsor Protocol Number: 80009 | Start Date*: 2022-06-28 |
Sponsor Name:University Medical Centre Utrecht Department of Vascular Surgery | ||
Full Title: A randomized placebo-controlled double-blind trial studying the effect of antiplatelet monotherapy (clopidogrel) versus dual antiplatelet therapy (clopidogrel + aspirin) on the occurrence of athero... | ||
Medical condition: (Chronic) Peripheral (occlusive) arterial disease (PAD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005383-14 | Sponsor Protocol Number: PROMIXDexamethasone | Start Date*: 2015-04-08 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: Protracted mixture of local anaesthetics for major foot and ankle surgery. A randomized double-blind, controlled study comparing Bupivacaine-epinephrine 0.5% and Bupivacaine-epinepherine 0.5% plus ... | |||||||||||||
Medical condition: The postoperative period after major foot and ankle surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004684-40 | Sponsor Protocol Number: N-O_CLI_Study | Start Date*: 2018-04-19 | |||||||||||
Sponsor Name:Krakowski Szpital Specjalistyczny im. Jana Pawła II | |||||||||||||
Full Title: Regeneration of ischemic damages in cardiovascular system using Wharton’s jelly as an unlimited source of mesenchymal stem cells for regenerative medicine. Project of the National Centre for Resear... | |||||||||||||
Medical condition: Critical limb ischemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000619-27 | Sponsor Protocol Number: 56481676 | Start Date*: 2007-08-13 | ||||||||||||||||
Sponsor Name:University Hospitals of Leicester NHS Trust | ||||||||||||||||||
Full Title: Prospective, double-blind, randomised trial to assess the efficacy of continuous sciatic/posterior tibial nerve blockade via a neural sheath catheter in lower limb amputees | ||||||||||||||||||
Medical condition: Stump and phantom limb pain after lower limb amputation | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-004068-21 | Sponsor Protocol Number: PADHIF00805 | Start Date*: 2006-01-11 |
Sponsor Name:Genzyme Europe BV | ||
Full Title: A Phase 2 Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Multi-Center Study of Ad2/Hypoxia Inducible Factor (HIF)-1alfa/VP16 Administered by Intramuscular Injection to Patients with ... | ||
Medical condition: Peripheral Arterial Disease (PAD) with no or poor Chronic Critical Limb Ischemia (CLI) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-001313-24 | Sponsor Protocol Number: SUPERADD | Start Date*: 2017-02-13 | ||||||||||||||||||||||||||
Sponsor Name:Technische Universität München, Fakultät für Medizin | ||||||||||||||||||||||||||||
Full Title: SUbstition of PERioperative Albumin Deficiency Disorders | ||||||||||||||||||||||||||||
Medical condition: High risk surgical patients or procedures showing a hypoalbuminemia intraoperatively. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-018173-31 | Sponsor Protocol Number: POISE-2 | Start Date*: 2011-02-25 | |||||||||||
Sponsor Name:Fundació Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau | |||||||||||||
Full Title: Ensayo clínico factorial de clonidina y aspirina en pacientes que van a ser sometidos a cirugía no cardiaca y que estén en riesgo moderado o alto de sufrir eventos cardíacos perioperatorios (Estudi... | |||||||||||||
Medical condition: Prevención de episodios cardiovasculares en pacientes de moderado a alto riesgo cardiovascular que son sometidos a una cirugía no cardiaca. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) AT (Completed) BE (Completed) DK (Completed) GB (Completed) DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
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