- Trials with a EudraCT protocol (24)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (244)
24 result(s) found for: Ephedrine.
Displaying page 1 of 2.
| EudraCT Number: 2009-013293-41 | Sponsor Protocol Number: 08/0182 | Start Date*: 2011-03-21 |
| Sponsor Name:Joint UCLH/UCH Biomedical Research Unit | ||
| Full Title: Randomised, double blind, phase IV study to compare the incidence of ECG changes during elective caesarean section under spinal anaesthesia when using phenylephrine or ephedrine infusion to maintai... | ||
| Medical condition: uncomplicated term pregnancy. Patient undergoing elective cesarean delivery. Ephedrine and phenylephrine are vasopressors used to maintain maternal blood pressure close to normal values during spin... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-002456-15 | Sponsor Protocol Number: ANE 05/06 | Start Date*: 2006-06-29 |
| Sponsor Name:UZ Leuven | ||
| Full Title: The influence of prophylactic ephedrine on arterial hypotension and fetal dysrhythmia after combined spinal-epidural anesthesia during labour | ||
| Medical condition: Comined spinal - epiural analgesia (CSE) during labour. | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-001355-23 | Sponsor Protocol Number: 40960 | Start Date*: 2014-08-29 | |||||||||||
| Sponsor Name:Leiden University Medical Center | |||||||||||||
| Full Title: Ephedrine as add-on therapy for patients with myasthenia gravis | |||||||||||||
| Medical condition: myasthenia gravis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-001839-13 | Sponsor Protocol Number: AGO/2016/006 | Start Date*: 2016-06-07 |
| Sponsor Name:Ghent University Hospital | ||
| Full Title: Influence of a bolus administration of ephedrine and phenylephrine on spinal oxygen saturation, measured with NIRS. | ||
| Medical condition: Hypotension during surgery Paraplegia and/or paraparesis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-003926-11 | Sponsor Protocol Number: MVDV 07/2007 | Start Date*: 2007-10-03 |
| Sponsor Name:University Hospitals Leuven | ||
| Full Title: Low dose of ephedrine versus phenylephrine in the prevention of arterial hypotension after low dosed CSE for elective C-section : is there a difference in umbilical blood gas values ? | ||
| Medical condition: combined spinal-epidural analgesia during C-section | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-000965-19 | Sponsor Protocol Number: 2019/374 | 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 equipotent prophylactic doses of ephedrine, phe... | ||
| Medical condition: Ephedrine, phenylephrine and norepinephrine are vasopressors used during anesthesia to treat hypotension. These agents raise blood pressure, but may have different effects on circulation as measure... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: NO (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-004232-66 | Sponsor Protocol Number: AOIFUTIER2011 | Start Date*: 2012-01-05 |
| Sponsor Name:CHU de Clermont-Ferrand | ||
| Full Title: | ||
| Medical condition: | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-001827-11 | Sponsor Protocol Number: RBHP_2012_GUESMI | Start Date*: 2013-05-03 |
| Sponsor Name:CHU de Clermont-Ferrand | ||
| Full Title: | ||
| Medical condition: | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-002734-19 | Sponsor Protocol Number: 2004066 | Start Date*: 2005-08-23 |
| Sponsor Name:South Tees Acute Hospitals NHS Trust | ||
| Full Title: Do the drugs that are normally used to treat low blood pressure during Caesarean section affect spread of spinal anaesthesia? | ||
| Medical condition: We plan to study women having elective, low-risk, Caesarean sections under spinal anaesthesia. Hypotension is very frequent with spinal anaesthesia in this patient population and it usually require... | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-006103-35 | Sponsor Protocol Number: SJ-271 | Start Date*: 2012-01-30 | |||||||||||
| Sponsor Name:Næstved hospital | |||||||||||||
| Full Title: The Oxygenation of the Brain DUring elective Caesarean section. A comparison of ephedrine versus phenylephrine | |||||||||||||
| Medical condition: Elective ceasarean section | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-004190-16 | Sponsor Protocol Number: 69HCL14-0248 | Start Date*: 2014-12-02 | |||||||||||
| Sponsor Name:Hospices Civils de Lyon | |||||||||||||
| Full Title: Determination of the optimal dose of ephedrine to treat hypotension during surgery of newborn to six months infant | |||||||||||||
| Medical condition: Arterial Hypotension | |||||||||||||
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| Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-003470-88 | Sponsor Protocol Number: 11-195 | Start Date*: 2012-07-30 | ||||||||||||||||
| Sponsor Name:University Medical Center Utrecht, The Netherlands | ||||||||||||||||||
| Full Title: Phenylephrine versus EPhedrine on cerebral Perfusion during carotid EndarteRectomy: PEPPER study | ||||||||||||||||||
| Medical condition: Hypotension during carotid endarterectomy | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2015-001359-60 | Sponsor Protocol Number: Vasobrain01 | Start Date*: 2015-06-16 | |||||||||||
| Sponsor Name:Aarhus University Hospital | |||||||||||||
| Full Title: Influence of vasopressors on brain oxygenation and microcirculation in anesthetized patients with cerebral tumors | |||||||||||||
| Medical condition: Brain oxygenation and microcirculation under administration of Efedrin and Metaoxedrin in patients with cerebral tumor. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2022-002892-12 | Sponsor Protocol Number: CHUB-VASO-IRC | Start Date*: 2022-09-13 | ||||||||||||||||
| Sponsor Name:CHU Brugmann | ||||||||||||||||||
| Full Title: Comparison of the efficacy of ephedrine versus norepinephrine in the treatment of hypotension occurring after induction of general anesthesia in patients with chronic renal failure: randomized doub... | ||||||||||||||||||
| Medical condition: Hypotension occurring post-induction of general anesthesia in patients with chronic renal failure during elective surgery. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2015-002843-32 | Sponsor Protocol Number: 54015 | Start Date*: 2016-09-20 |
| Sponsor Name: | ||
| Full Title: The haemodynamic effects of spinal anaesthesia with versus without sufentanil added to bupivacaine heavy | ||
| Medical condition: Patient undergoing surgery for which they receive spinal anaesthesia | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| 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: 2018-003182-34 | Sponsor Protocol Number: 2018-10 | Start Date*: 2018-10-18 |
| Sponsor Name:CHR d'ORLEANS | ||
| Full Title: Randomized, double-blind, controlled clinical trial for comparison of continuous phenylephrine versus norepinephrine infusion for maintenance of hemodynamic stability during cesarean section under... | ||
| Medical condition: hypotension during caesarean section under spinal anesthesia | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-005576-32 | Sponsor Protocol Number: Argo01-05 | Start Date*: 2005-12-19 | |||||||||||
| Sponsor Name:BRACCO | |||||||||||||
| Full Title: TOLERABILITY OF A NEW FORMULATION OF ARGOTONE IN HEALTH VOLONTEERS | |||||||||||||
| Medical condition: Rhinitis and nasal congestion | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-000727-12 | Sponsor Protocol Number: RC31/20/0443 | Start Date*: 2021-06-28 |
| Sponsor Name:University Hospital of Toulouse | ||
| Full Title: Quality Assessment of Tracheal intubation without neuromuscular blocking drugs (Propofol+ Remifentanil) in obese patients: Pilot Study | ||
| Medical condition: induction phase of the general anesthesia in obese patients | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-004512-22 | Sponsor Protocol Number: P2018/568 | Start Date*: 2019-02-18 |
| Sponsor Name:Erasme University Hospital | ||
| Full Title: Effect of dexmedetomidine vs 0.9% sodium chloride on Nol-Index guided remifentanil analgesia: a double-blinded bicenter randomized controlled trial | ||
| Medical condition: Intraoperative analgesia during general anesthesia | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: BE (Completed) | ||
| Trial results: (No results available) | ||
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