- Trials with a EudraCT protocol (69)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (71)
69 result(s) found for: Phenylephrine.
Displaying page 1 of 4.
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: 2006-004858-25 | Sponsor Protocol Number: RF01 | Start Date*: 2007-02-16 |
Sponsor Name:Royal Free Hampstead NHS Trust | ||
Full Title: Study to compare maternal cardiovascular stability with different phenylephrine dosing regimens used to maintain baseline systolic blood pressure following a spinal anaesthetic for elective caesare... | ||
Medical condition: We are studying healthy pregnant women undergoing planned caesarean section under spinal anaesthesia. We are investigating ways of reducing hypotension due to spinal anaesthesia by comparing 3 diff... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Completed) | ||
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: 2020-000573-25 | Sponsor Protocol Number: 1.1 | Start Date*: 2020-03-20 |
Sponsor Name:Aarhus University Hospital | ||
Full Title: Evaluation of patients after cardiac surgery: Novel ultrasound parameters for quantification of renal perfusion & analysis of phenylephrines’ effect on invasive haemodynamics and echocardiographic ... | ||
Medical condition: Hypotension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-003687-31 | Sponsor Protocol Number: AGO/2018/005 | Start Date*: 2019-01-31 |
Sponsor Name:Ghent University Hospital | ||
Full Title: Influence of continuous administration of phenylephrine versus dobutamine on spinal oxygen saturation, measured with near-infrared spectroscopy (NIRS). | ||
Medical condition: spinal vasculature spinal oxygen saturation muscle oxygen saturation cerebral oxygen saturation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-002339-23 | Sponsor Protocol Number: MydriasisbeiMydrane | Start Date*: 2019-10-24 |
Sponsor Name:Medical University Graz, Department of Ophtalmology | ||
Full Title: Prospective intraindividual comparison of the mydriasis of a standardized intracameral anaesthetics with the topical preoperative drop application in the uncomplicated cataract surgery | ||
Medical condition: patients who need a cataract surgery in both eyes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2022-001023-32 | Sponsor Protocol Number: RACE_01 | Start Date*: 2022-09-14 |
Sponsor Name:Medical University of Vienna | ||
Full Title: The effect of epinephrine, norepinephrine and phenylephrine on intraoperative hemodynamic performance - a prospective double-blinded, randomized clinical trial | ||
Medical condition: Patients > 45 years of age at-risk for cardiovascular complications undergoing moderate- to high-risk major open abdominal surgery. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2009-013543-11 | Sponsor Protocol Number: 2009057 | Start Date*: 2009-10-19 |
Sponsor Name:James Cook University Hospital | ||
Full Title: A comparison of nausea with two routine ways of managing low blood pressure after delivery of the baby during spinal anaesthesia for Caesarean section. | ||
Medical condition: We are investigating nausea associated with hypotension caused by spinal anaesthesia in healthy women undergoing elective Caesarean section. NICE recommend phenylephrine in this population. The aim... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004309-27 | Sponsor Protocol Number: P04579 | Start Date*: 2005-12-28 |
Sponsor Name:Schering Plough Research Institute | ||
Full Title: Cross-Over Study of the Decongestant Effect of Phenylephrine Compared With Placebo and Pseudoephedrine as Active Control in SAR Subjects Exposed to Pollen in the Vienna Challenge Chamber | ||
Medical condition: Seasonal Allergic Rhinitis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (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: 2015-003064-36 | Sponsor Protocol Number: DEF_Version_1.2 | Start Date*: 2015-11-10 |
Sponsor Name:Vienna Institute for Research in Ocular Surgery | ||
Full Title: Impact of selective alpha 1A receptor antagonists on the pupil size after instillation of tropicamide 0.5% and phenylephrine 10% | ||
Medical condition: Impact of selective alpha 1A receptor antagonists on the pupil size after instillation of tropicamide 0.5% and phenylephrine 10% | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002385-23 | Sponsor Protocol Number: AFT-MXCF-03 | Start Date*: 2015-11-10 | |||||||||||
Sponsor Name:AFT Pharmaceuticals Ltd | |||||||||||||
Full Title: A phase 3 randomised, double blind, multiple dose, parallel group efficacy study of different doses of phenylephrine hydrochloride combined with paracetamol and/or ibuprofen in participants with na... | |||||||||||||
Medical condition: nasal congestion | |||||||||||||
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Population Age: Adults | Gender: Male, 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: 2013-005617-13 | Sponsor Protocol Number: MVDV122013 | Start Date*: 2014-05-27 | |||||||||||
Sponsor Name:University Hospitals Leuven | |||||||||||||
Full Title: Determination of the equivalent dose of phenylephrine and Akrinor in the prevention of post-spinal hypotension during Cesarean section. | |||||||||||||
Medical condition: post-spinal hypotension | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
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: 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: 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: 2013-000292-33 | Sponsor Protocol Number: HGC_SAR_1_13 | Start Date*: 2013-11-07 | ||||||||||||||||
Sponsor Name:Laura Sararols Ramsay | ||||||||||||||||||
Full Title: Comparative study of the mydriatic effect of Mydriasert vs the use of topical instillation of phenylephrine (10%) and tropicamide (1%) before catarcat surgery. | ||||||||||||||||||
Medical condition: Cataract surgery | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-005576-33 | Sponsor Protocol Number: LT2380-PII-09/12 | Start Date*: 2013-09-03 |
Sponsor Name:Laboratoires Théa | ||
Full Title: Efficacy and safety assessment of intracameral T2380 (Fixed combination of lidocaïne, phenylephrine and tropicamide) to obtain mydriasis in patients with small pupils for cataract surgery by phacoe... | ||
Medical condition: The primary aim of this study is to evaluate mydriasis obtained with T2380 (Fixed combination of lidocaïne, phenylephrine and tropicamide) in patients with small pupils | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
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 |
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