- Trials with a EudraCT protocol (9)
 - Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
 
		
	   		
	   		    
                    
                   	
                   	    9 result(s) found for: Amputation stump.
                    
                
			
   			
		
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| EudraCT Number: 2008-002655-24 | Sponsor Protocol Number: SMR-1850/2PX-SP-02 | Start Date*: 2008-09-30 | |||||||||||
| Sponsor Name:SantoSolve A/S | |||||||||||||
| Full Title: A randomised, double-blind, placebo (vehicle) controlled, parallel group study of the efficacy, safety and tolerability of topical 2PX (strontium chloride hexahydrate) in patients with chronic, mod... | |||||||||||||
| Medical condition: Post amputation patients (at least 6 months prior to visit 1) with chronic moderate-to-severe lower limb stump pain, defined as average stump pain on a daily basis (≥40 on a 100 mm pain VAS scale) ... | |||||||||||||
					
						
							
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| Population Age: | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) GB (Prematurely Ended) DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-004293-10 | Sponsor Protocol Number: REH-TOX-2013-01 | Start Date*: 2014-06-03 | |||||||||||
| Sponsor Name:Hospital Universitari de Tarragona Joan XXIII | |||||||||||||
| Full Title: Efficacy of treatment by iontophoresis of botulinum toxin type A free from complexing proteins for stump hyperhidrosis | |||||||||||||
| Medical condition: Stump hyperhidrosis in lower limb amputees | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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 (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-003807-20 | Sponsor Protocol Number: FinAPain-1 | Start Date*: 2014-02-28 | |||||||||||
| Sponsor Name:HUS, Leikkaus- ja anestesiaosasto | |||||||||||||
| Full Title: Periferal local anesthetic infusion for postoperative pain after above knee amputation | |||||||||||||
| Medical condition: Pain after amputation above knee | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| 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: 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: 2008-005470-12 | Sponsor Protocol Number: Calc01 | Start Date*: 2009-05-11 | |||||||||||
| Sponsor Name:Medical University of Vienna | |||||||||||||
| Full Title: Calcitonin Prophylaxis in Phantom Limb Pain | |||||||||||||
| Medical condition: Almost 60% of patients suffer from phantom limb pain one year after surgery, whereas in the first month, 85% to 97% of patients experience phantom limb pain. IV. calcitonin in the early postoperati... | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-003544-37 | Sponsor Protocol Number: ABUHB/01/0816/1 | Start Date*: 2016-11-30 | ||||||||||||||||||||||||||
| Sponsor Name:Aneurin Bevan University Health Board | ||||||||||||||||||||||||||||
| Full Title: Perineural Local Anaesthetic Catheter aftEr Major lowEr limb amputatioN Trial (PLACEMENT) | ||||||||||||||||||||||||||||
| Medical condition: Analgesia for lower limb amputation for peripheral vascular disease (PVD) | ||||||||||||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2010-024265-40 | Sponsor Protocol Number: KETA-FAN | Start Date*: 2011-10-27 | |||||||||||
| Sponsor Name:HOSPITAL UNIVERSITARI DE BELLVITGE | |||||||||||||
| Full Title: Perineural vs systemic N-methyl-D-aspartate (NMDA) receptors antagonism with ketamine as a reverser of peripheral and central sensitization in phantom limb pain | |||||||||||||
| Medical condition: Phantom limb pain | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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