- Trials with a EudraCT protocol (50)
 - Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
 
		
	   		
	   		    
                    
                   	
                   	    50 result(s) found for: Muscle relaxation.
                    
                
			
   			
		
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	| EudraCT Number: 2013-002164-53 | Sponsor Protocol Number: 20130513 | Start Date*: 2013-12-02 | 
| Sponsor Name:Medizinische Universität Wien, Abteilung für Allgemeine Anästhesie und Intensivmedizin | ||
| Full Title: The reversed isolated forearm technique to regionally reverse rocuronium induced muscle relaxation – a pilot study | ||
| Medical condition: To evaluate the feasibility of regionally reversing a rocuronium induced muscle relaxation and to determine the dose of sugammadex that is necessary to reach a train of four (TOF) ratio ≥ 0.9. To d... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2022-003737-19 | Sponsor Protocol Number: CHUB-ITF-sevo-propofol | Start Date*: 2023-01-10 | 
| Sponsor Name:CHU Brugmann | ||
| Full Title: Influence of sevoflurane and propofol on maximum muscular strength, speed of contraction and relaxation, in humans: A pilot study. | ||
| Medical condition: Impact of anesthetic drugs on neuromuscular transmission | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-005010-40 | Sponsor Protocol Number: 30082007 | Start Date*: 2008-03-13 | |||||||||||
| Sponsor Name:Univ.-Prof. Dr. Volker Wenzel | |||||||||||||
| Full Title: Arginin Vasopressin im fortgeschrittenen vasodilatorischen Schock: Ein Dosisvergleich 2 vs. 4 IU/h | |||||||||||||
| Medical condition: 5. Einschlusskriterien 5.1. Patienten mit vasodilatorischem Schock aufgrund: a) Sepsis [Definitionen gemäss den Empfehlungen der ACCP/SCCM (12)] b) SIRS [Definitionen gemäss den Empfehlungen der ... | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-001597-16 | Sponsor Protocol Number: none | Start Date*: 2018-07-18 | |||||||||||
| Sponsor Name:Sitnikova Victoria | |||||||||||||
| Full Title: Efficacy of botulinum toxin in treating temporomandibular disorders | |||||||||||||
| Medical condition: Patients are diagnosed TMD (temporomandibular disorder) according to DC/TMD international consortium: myalgia, local myalgia, myofascial pain, myofascial pain with referral. | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-000462-62 | Sponsor Protocol Number: Statex1 | Start Date*: 2015-09-23 | 
| Sponsor Name:Radboud university medical centre | ||
| Full Title: The effects of statins on skeletal muscle mitochondria: is exercise the medicine? | ||
| Medical condition: Asymp and symp statin users will undergo baseline measurements of skeletal muscle mitochondrial function and muscle function after which they will be switched to a single-blind placebo intervention... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-015771-27 | Sponsor Protocol Number: V3 | Start Date*: 2010-01-21 | 
| Sponsor Name:Medizinische Universität Wien, Univ.Klinik für Notfallmedizin | ||
| Full Title: Requirement of Skeletal Muscle Paralysis in Hypothermic Patients after Cardiac Arrest. A pilot study | ||
| Medical condition: skeletal muscle paralysis in hypothermic patients after cardiac arrest | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-002147-18 | Sponsor Protocol Number: ABR49503 | Start Date*: 2015-07-02 | 
| Sponsor Name:Academic Medical Center | ||
| Full Title: A randomized controlled double-blinded trial comparing the effect of on Demand ROcuronium boluses vs continuous infusion on rating of surgical and anesthesia conditions and need for reversal in Pat... | ||
| Medical condition: oesophageal carcinoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-000029-29 | Sponsor Protocol Number: 95105003 | Start Date*: 2018-12-11 | 
| Sponsor Name:VU University Medical Center | ||
| Full Title: Extra energy for hearts with a genetic defect: ENERGY trial | ||
| Medical condition: Hypertrophic cardiomyopathy | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-001155-22 | Sponsor Protocol Number: Lap2014NMB | Start Date*: 2014-05-22 | ||||||||||||||||
| Sponsor Name:Mona Ring Gätke | ||||||||||||||||||
| Full Title: Muscle relaxation during open upper abdominal surgery -can the surgical conditions be optimized? (The laparotomy study) | ||||||||||||||||||
| Medical condition: The aim of the study is to investigate if intense NMB improves surgical conditions during operation in patients scheduled for elective open upper abdominal surgery. | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2009-012815-16 | Sponsor Protocol Number: ROSANNA | Start Date*: 2010-03-18 | ||||||||||||||||
| Sponsor Name:Technische Universität München | ||||||||||||||||||
| Full Title: Dosis-Wirkungsstudie von Rocuronium unter Propofol-Anästhesie (Rocuronium Dose Finding Study after single shot or steady state propofol anesthesia) | ||||||||||||||||||
| Medical condition: Rocuronium dose finding study; evaluation of effective doses (ED 50 and ED 95) of rocuronium after single shot or steady state propofol anesthesia | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2013-001965-17 | Sponsor Protocol Number: AITT2013/5 | Start Date*: 2013-09-26 | |||||||||||
| Sponsor Name:Debreceni Egyetem Orvos- és Egészségtudományi Centrum Aneszteziológiai és Intenzív Terápiás Tanszék | |||||||||||||
| Full Title: Incidence of postoperative residual neuromuscular blockade following the administration of rocuronium: A randomized placebo controlled study. | |||||||||||||
| Medical condition: The effect of sugammadex and neostigmin on postoperative residual neuromuscular blockade will be investigated, therefore the patients suffering from various conditions undergoing surgery in general... | |||||||||||||
					
						
							
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-001732-21 | Sponsor Protocol Number: MET001 | Start Date*: 2013-09-06 | 
| Sponsor Name:Centre d'Etude des Cellules Souches (CECS) | ||
| Full Title: A randomized, double blind, placebo-controlled phase II study of metformin in myotonic dystrophy type 1 patients | ||
| Medical condition: Myotonic dystrophy type 1 (DM1) also known as Steinert disease | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-001886-33 | Sponsor Protocol Number: MK-8616-076-00 | Start Date*: 2012-10-30 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
| Full Title: Randomized, Controlled, Parallel Group, Double Blind Trial to Compare the Use of Deep or Standard Neuromuscular Blockade in Combination With Low or Standard Insufflation Pressures Using a 2x2 Fact... | |||||||||||||
| Medical condition: Patients undergoing elective in-patient laparoscopic cholecystectomy procedures under general anesthesia with neuromuscular relaxation and active reversal of neuromuscular blockade | |||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) FI (Completed) GB (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002961-21 | Sponsor Protocol Number: NS918 | Start Date*: 2018-11-09 | 
| Sponsor Name:UZ Leuven | ||
| Full Title: The effect of deep neuromuscular block and reversal with sugammadex on surgical conditions and perioperative morbidity in shoulder surgery using a deltopectoral approach | ||
| Medical condition: Subject undergoing elective or semi-elective surgery to the gleno-humeral joint or the proximal humerus using a deltoideo-pectoral approach. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-003033-42 | Sponsor Protocol Number: EURO-RELAX | Start Date*: 2020-01-28 | 
| Sponsor Name:INSTITUTO DE INVESTIGACIÓN SANITARIA LA FE | ||
| Full Title: The impact of deep versus standard muscle relaxation on intra-operative safety during laparoscopic surgery: a multicenter strategy study – EURO RELAX STUDY | ||
| Medical condition: Intra-operative adverse events during laparoscopic surgery | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-003385-24 | Sponsor Protocol Number: 2815 | Start Date*: 2016-09-28 | 
| Sponsor Name:GGZ inGeest, parner VUmc | ||
| Full Title: The Recall-study: Rivastigmine for ECT-induced Cognitive Adverse effects in Late Life Depression: a multicenter, randomized, double-blind, placebo-controlled, crossover trial | ||
| Medical condition: Interictal delirium during electric convulsive therapy- course | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-001164-29 | Sponsor Protocol Number: NMBDK2013 | Start Date*: 2013-05-15 | ||||||||||||||||
| Sponsor Name:Department of anesthesiology | ||||||||||||||||||
| Full Title: Optimizing surgical conditions: Intraabdominal distance during gynecologic laparoscopic surgery with and without muscle relaxation (The measurement study) | ||||||||||||||||||
| Medical condition: To investigate if deep neuromucular blockade improves intraabdominal volume compared to no neuromuscular blockade in patients scheduled for gynecologic laparoscopic surgery with pneumoperitoneum 12... | ||||||||||||||||||
					
						
							
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2005-005050-47 | Sponsor Protocol Number: 19.4.304 | Start Date*: 2006-01-24 | 
| Sponsor Name:NV Organon | ||
| Full Title: A multi-center, parallel-group, comparative trial evaluating the efficacy, pharmacokinetics and safety of Org 25969 in subjects with normal or impaired renal function. | ||
| Medical condition: Not Applicable | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-003787-51 | Sponsor Protocol Number: NMBDK2012 | Start Date*: 2012-10-22 | 
| Sponsor Name:Mona Ring Gätke | ||
| Full Title: Recovery after laparoscopic hysterectomy with deep neuromuscular blockade and low intraabdominal pressure | ||
| Medical condition: The pain study: To evaluate the importance of deep neuromuscular blockade (NMB) and low intraabdominal pressure in laparoscopic hysterectomy considering postoperative pain, nausea, consumption of ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-003623-29 | Sponsor Protocol Number: 63227.091.17 | Start Date*: 2018-03-27 | 
| Sponsor Name:Radboudumc | ||
| Full Title: MRI measurement of the effects of moderate versus deep neuromuscular blockade on the abdominal working space during laparoscopic surgery in a prospective cohort study. | ||
| Medical condition: We will investigate the effect of deep neuromuscular blockade on the abdominal working space. We will include patients undergoing laparoscopic surgery, including laparoscopic donor nephrectomy, lap... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
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