- Trials with a EudraCT protocol (145)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (11)
145 result(s) found for: Remifentanil.
Displaying page 1 of 8.
| EudraCT Number: 2015-000051-24 | Sponsor Protocol Number: RemiPedEntropy_v1.0 | Start Date*: 2015-03-26 |
| Sponsor Name:Klaus Olkkola/University of Helsinki | ||
| Full Title: The pharmacokinetics and –genomics of remifentanil, and its effects on the depth-of-anaesthesia monitors and the protein synthesis in children. | ||
| Medical condition: otherwise healthy patients undergoing an operation necessitating general anaesthesia | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: FI (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-000961-19 | Sponsor Protocol Number: 2019/376 | Start Date*: 2019-08-26 |
| Sponsor Name:Helse Fonna | ||
| Full Title: “Haemodynamic stability during induction of general anesthesia with propofol and remifentanil: A randomized, controlled, double-blind study comparing medium and low remifentanil doses.” | ||
| Medical condition: In daily clinical work we observe a hypotensive effect and a reduction in heart rate when induction of general anesthesia is performed using propofol and remifentanil. It is difficult to differenti... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: NO (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-004346-10 | Sponsor Protocol Number: N/A | Start Date*: 2015-04-15 |
| Sponsor Name:Alder Hey Children's NHS Foundation Trust | ||
| Full Title: Study to evaluate the optimal dose of remifentanil infusion(effective dose in 80% of patients) required to ensure apnoea (of 30 seconds duration) during magnetic resonance imaging of the heart unde... | ||
| Medical condition: Study refers to the use of this medicine during anaesthesia given during the investigation of congenital heart disease. | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-000597-21 | Sponsor Protocol Number: REMISYD | Start Date*: 2008-05-27 |
| Sponsor Name:Kuopio University Hospital, Anesthesiology Clinic | ||
| Full Title: Requirement of analgesics after two remifentanil dosing regimen in cardiac surgery. | ||
| Medical condition: Post-operative requirement of analgesics in relation to remifentanil dose administered during cardiac surgery is to be investigated. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-018233-21 | Sponsor Protocol Number: WEC 0910 | Start Date*: 2010-03-31 |
| Sponsor Name:Leiden University Medical Centre | ||
| Full Title: Modeling the respiratory effects of subanesthetic doses of propofol under closed-loop or non-steady-state conditions without and with a remifentanil background infusion in healthy volunteers. | ||
| Medical condition: This study is performed in healthy volunteers. The study is aimed at investigating the effect of propofol and remifentanil-propofol interaction on breathing in awake, non-artificially ventilated vo... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-020042-94 | Sponsor Protocol Number: LS07-040 | Start Date*: 2010-09-02 |
| Sponsor Name:Medizinische Universität Wien, Universitätsklinik für Anästhesie, Allgemeine Intensivmedizin | ||
| Full Title: The Effect of High-dose Remifentanil on the Reversal of Neuropathic Pain in Postherpetic Patients | ||
| Medical condition: Post herpetic hyperalgesia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-002533-10 | Sponsor Protocol Number: SuRe-001 | Start Date*: 2013-05-22 |
| Sponsor Name:UMCG | ||
| Full Title: Comparison of the effects of atropine on haemodynamics and tissue oxygenation in anaesthesia with propofol and sufentanil versus propofol and remifentanil’ | ||
| Medical condition: Comparison of the effects of atropine on haemodynamics and tissue oxygenation in anaesthesia with propofol and sufentanil versus propofol and remifentanil | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-000958-56 | Sponsor Protocol Number: 2019/375 | Start Date*: 2019-08-16 |
| Sponsor Name:Helse Fonna | ||
| Full Title: “Haemodynamic stability during induction of general anesthesia with propofol and remifentanil: A randomized, controlled, double-blind study comparing low vs high propofol doses.” | ||
| Medical condition: In daily clinical work we observe a hypotensive effect and a reduction in HR when induction of general anesthesia is performed using propofol and remifentanil. It is difficult to differentiate the ... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: NO (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-007972-70 | Sponsor Protocol Number: 11/2008 FDB | Start Date*: 2009-01-22 |
| Sponsor Name:University Hospital Leuven | ||
| Full Title: Transplacentar pharmacokinetics of remifentanil | ||
| Medical condition: Transplacentar pharmacokinetics of Remifentanil | ||
| Disease: | ||
| Population Age: In utero, Under 18 | Gender: Female | |
| Trial protocol: BE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-004479-38 | Sponsor Protocol Number: REG 31/05 | Start Date*: 2006-01-12 |
| Sponsor Name:AZIENDA OSPEDALIERA "OSPEDALI RIUNITI DI BERGAMO" (A.O. DI RILIEVO NAZIONALE) | ||
| Full Title: Effects of the association remifentanil-propofol in TCI on the respiratory exchanges: comparison between controlled and spontaneous ventilation | ||
| Medical condition: general anesthesia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: IT (Completed) | ||
| Trial results: (No results available) | ||
| 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: 2007-003151-36 | Sponsor Protocol Number: AGO/2007/006 | Start Date*: 2007-08-01 |
| Sponsor Name:University Hospital Ghent | ||
| Full Title: Sevoflurane-Remifentanil interaction: Multiple response surfaces, validation of calibration stimuli, validation of the intraoperative isobole concept and investigating remifentanil induced opioid t... | ||
| Medical condition: American Society of Anesthesia class I and II patients scheduled for surgery under general anesthesia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-007322-19 | Sponsor Protocol Number: RPC190 | Start Date*: 2009-07-07 |
| Sponsor Name:Queen Victoria Hospital NHS Foundation Trust | ||
| Full Title: A Comparison of Remifentanil Patient-Controlled Analgesia vs. Oral Morphine Analgesia for Dressing Changes in Burns Patients. | ||
| Medical condition: Pain experienced by patients with pre-existing burns presenting to the burns outpatients unit requiring two or more dressing changes | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-001677-81 | Sponsor Protocol Number: PTRS01 | Start Date*: 2019-11-27 |
| Sponsor Name:Akershus Universitetssykehus | ||
| Full Title: Remifentanil tapering and post-adenotonsillectomy pain in children: a randomised, placebo controlled, double blind study | ||
| Medical condition: Tonsillectomy and adenotonsillectomy | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: NO (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-000962-23 | Sponsor Protocol Number: REDEX | Start Date*: 2014-07-10 |
| Sponsor Name:Consorci Parc de Salut Mar | ||
| Full Title: Effect of dexmedetomidine on monitoring of motor evoked potentials in patients undergoing supratentorial craniotomy or brainstem surgery | ||
| Medical condition: Patients scheduled for supratentorial craniotomy or brainstem surgery with intraoperative monitoring of motor evoked potentials (MEP). | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-005257-22 | Sponsor Protocol Number: RG_12-151 | Start Date*: 2013-07-12 |
| Sponsor Name:University of Birmingham | ||
| Full Title: Remifentanil intravenous patient controlled analgesia (PCA) versus intramuscular pethidine for pain relief in labour: a randomised controlled trial | ||
| Medical condition: Childbirth | ||
| Disease: | ||
| Population Age: | Gender: Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2013-003220-36 | Sponsor Protocol Number: 45112 | Start Date*: 2014-05-21 |
| Sponsor Name:Albert Schweitzer hospital | ||
| Full Title: Remifentanil use for procedural sedation and analgesia in the emergency department | ||
| Medical condition: The research will be conducted in patients that need short painfull treatment in the emergency department and with an indication for PSA. These treatments include: repositioning of fractures, repos... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-002883-20 | Sponsor Protocol Number: WALIBI-001 | Start Date*: 2013-09-30 |
| Sponsor Name:University Medical Center Groningen | ||
| Full Title: Walking the Isobole of drug Interaction: Comparison of hemodynamic effects, cerebral and tissue oxygenation for 4 equipotent combinations of propofol and remifentanil | ||
| Medical condition: elective ophthalmic surgery under general anesthesia. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-000877-23 | Sponsor Protocol Number: JM/JS/4551 | Start Date*: 2005-04-11 |
| Sponsor Name:Oxford Radcliffe Hospitals NHS trust | ||
| Full Title: Is Remifentanil better than Propofol in providing optimal conditions for an awake fibreoptic intubation? | ||
| Medical condition: Awake fibre optic intubation is an anaesthetic technique used to intubate patients with a difficult to manage airway. It s a procedure by which a tracheal tube is inserted in a patients trachea wh... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-000736-10 | Sponsor Protocol Number: | Start Date*: 2007-11-05 | |||||||||||
| Sponsor Name: | |||||||||||||
| Full Title: A comparison of pethidine/meperidine intramusculary and remifentanil patient-controlled analgesia during labor in Westfriesgasthuis | |||||||||||||
| Medical condition: Women in labour | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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