- Trials with a EudraCT protocol (82)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
82 result(s) found for: Rocuronium.
Displaying page 1 of 5.
| EudraCT Number: 2004-002715-92 | Sponsor Protocol Number: RKM/MS 01.06 | Start Date*: 2006-09-18 |
| Sponsor Name:Royal Group Hospitals | ||
| Full Title: A randomised, control, assessor blinded, dose escalating study to compare high dose rocuronium and suxamethonium for use in rapid sequence induction of anaesthesia | ||
| Medical condition: Patients undergoing Anaesthesia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| 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: 2019-004121-25 | Sponsor Protocol Number: NMBA_ELDERLY2019ROCU_REMI | Start Date*: 2019-12-17 | |||||||||||
| Sponsor Name:Rigshospitalet | |||||||||||||
| Full Title: A single-blinded multicenter randomized study comparing intubating conditions after either rocuronium 0.6 mg/kg or remifentanil 2 µg/kg in elderly patients. | |||||||||||||
| Medical condition: The aim of this study is to determine the effect on intubating conditions and laryngeal morbidity after either rocuronium 0.6 mg/kg or remifentanil 2 µg/kg in patients with age ≥ 80 years. | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-004343-76 | Sponsor Protocol Number: NMBA_ELDERLY2019ROCU_DOSES | Start Date*: 2020-02-27 | |||||||||||
| Sponsor Name:Rigshospitalet | |||||||||||||
| Full Title: A single-blinded multicenter randomized interventional study of rocuronium 0.3 mg/kg, and 0.9 mg/kg comparing onset time, duration of action and effect on intubating conditions in elderly patients ... | |||||||||||||
| Medical condition: The aim of this study is to determine the onset time, duration of action and effect on intubating conditions after rocuronium 0.3 mg/kg and 0.9 mg/kg in patients with age ≥ 80 years. | |||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (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: 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: 2006-004072-12 | Sponsor Protocol Number: 19.4.312 | Start Date*: 2007-02-01 |
| Sponsor Name:NV Organon | ||
| Full Title: A multi-center, randomized, parallel-group, safety assessor-blinded trial comparing efficacy and safety of 4.0 mg.kg-1 Org 25969, administered at T1 3-10% after continuous infusion of rocuronium, a... | ||
| Medical condition: Not applicable | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DK (Prematurely Ended) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-000709-55 | Sponsor Protocol Number: SugaRoc | Start Date*: 2020-04-01 |
| Sponsor Name:Universitair Ziekenhuis Brussel | ||
| Full Title: Sugammadex dose-finding study for reversal of deep rocuronium-induced neuromuscular block | ||
| Medical condition: decurarisation | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-002911-18 | Sponsor Protocol Number: 19.4.313 | Start Date*: 2007-09-05 |
| Sponsor Name:NV Organon | ||
| Full Title: Comparison of the T4/T1 ratio measured by means of the TOF-Watch® SX with the reappearance of T4 measured by means of a peripheral nerve stimulator in adult subjects receiving 4.0 mg.kg-1 sugammade... | ||
| Medical condition: Not applicable | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-006934-33 | Sponsor Protocol Number: 19.4.333 | Start Date*: 2008-04-02 |
| Sponsor Name:NV Organon | ||
| Full Title: A single center, open-label trial in subjects with severe renal impairment evaluating the dialysability of the sugammadex-rocuronium complex | ||
| Medical condition: Not applicable | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-005207-15 | Sponsor Protocol Number: 1 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Region Skåne | ||
| Full Title: Low dose muscle relaxant in intubation in children | ||
| Medical condition: | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-001133-15 | Sponsor Protocol Number: 19.4.208B | Start Date*: 2005-09-08 |
| Sponsor Name:NV Organon | ||
| Full Title: A multi-center, randomized, open-label, prospective bridging, parallel dosefinding trial comparing efficacy, safety and pharmacokinetics of 4 doses of Org 25969 and placebo administered at reappear... | ||
| Medical condition: Not applicable | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) BE (Completed) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-003005-27 | Sponsor Protocol Number: 2007-987 | Start Date*: 2007-09-27 | ||||||||||||||||
| Sponsor Name:Dept. of Anaesthesia, Centre of Head and Orthopaedics, Copenhagen University Hospital Rigshospitalet | ||||||||||||||||||
| Full Title: Pharmacodynamic trial on rocuronium in obese patients | ||||||||||||||||||
| Medical condition: Laparoscopic gastric banding or gastric bypass in propofol/remifentanil anaesthesia | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2005-001134-32 | Sponsor Protocol Number: 19.4.209B | Start Date*: 2005-08-18 |
| Sponsor Name:NV Organon | ||
| Full Title: A multi-center, randomized, open-label, prospective bridging, parallel dosefinding trial comparing efficacy and safety of 5 doses of Org 25969 administered at 1-2 PTC after rocuronium or vecuronium... | ||
| Medical condition: Not applicable | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-010840-33 | Sponsor Protocol Number: 09005RM-CSRVH | Start Date*: 2009-08-17 |
| Sponsor Name:BELFAST HEALTH & SOCIAL CARE TRUST | ||
| Full Title: Time to resumption of spontaneous respiration in patients administered either suxamethonium or rocuronium followed by sugammadex | ||
| Medical condition: Assessment of time to return of spontaneous ventilation after administration of either suxamethonium or rocuronium followed by sugammadex in patients undergoing planned surgery. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-002528-10 | Sponsor Protocol Number: SIVAA01 | Start Date*: 2017-07-06 |
| Sponsor Name:Vestfold Hospital Trust | ||
| Full Title: TOF trial: A randomized double blinded controlled Trial comparing low dose Of sugammadex and neostigmine aFter use of rocuronium during general anesthesia in patients undergoing non-cardiac surgery | ||
| Medical condition: The study population will include all patients >18 years scheduled for an elective surgical procedure undergoing general anesthesia with intravenous drugs and non-depolarizing NMBA (rocuronium), wi... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-007162-38 | Sponsor Protocol Number: 19.4.335 | Start Date*: 2008-03-17 |
| Sponsor Name:NV Organon | ||
| Full Title: A multi-center, open label trial, to show efficacy and safety of 4.0 mg.kg-1 sugammadex administered at a depth of neuromuscular blockade of 1-2 PTC induced by rocuronium in Chinese and European AS... | ||
| Medical condition: Not applicable | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DK (Completed) BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-001668-21 | Sponsor Protocol Number: FDE_2014_25 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Fondation Ophtalomologique A. de Rothschild | |||||||||||||
| Full Title: Addition of neuromuscular-blocking agents during induction in infants: potential interest in reducing hypoxia episodes | |||||||||||||
| Medical condition: Chirurgie programmée sous anesthésie générale avec intubation orotrachéale, avec induction inhalatoire prévue | |||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-001396-39 | Sponsor Protocol Number: 2011-411 | Start Date*: 2011-06-01 | |||||||||||
| Sponsor Name:Glostrup Hospital | |||||||||||||
| Full Title: | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2004-003819-23 | Sponsor Protocol Number: 19.4.306 | Start Date*: 2005-04-04 |
| Sponsor Name:NV Organon | ||
| Full Title: A multi-center, randomized, parallel dose-finding, safety-assessor blinded trial to explore the efficacy, safety and pharmacokinetics of four doses of Org 25969 and placebo in pediatric and adult s... | ||
| Medical condition: not applicable | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: FI (Completed) DE (Completed) GB (Completed) | ||
| Trial results: View results | ||
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