- Trials with a EudraCT protocol (8)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
8 result(s) found for: Paramedics.
Displaying page 1 of 1.
| EudraCT Number: 2014-005286-69 | Sponsor Protocol Number: 7502 | Start Date*: 2015-02-23 |
| Sponsor Name:Kuopion yliopistollinen sairaala/Ensihoitokeskus | ||
| Full Title: Intranasal fentanyl in pre-hospital analgesia | ||
| Medical condition: Patients with trauma, musculoskeletal, stomach or back pain on numeric rating scale at least value 4 | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-000154-10 | Sponsor Protocol Number: SOC.12/19-20 | Start Date*: 2020-10-14 |
| Sponsor Name:University of Warwick | ||
| Full Title: Paramedic Analgesia Comparing Ketamine and MorphiNe in trauma | ||
| Medical condition: Severe pain after traumatic injury | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-002308-40 | Sponsor Protocol Number: IN Morphine II | Start Date*: 2005-08-19 |
| Sponsor Name:University of Plymouth | ||
| Full Title: Evaluation of Intranasal (IN) Morphine Sulphate as a Paramedic Administered Analgesic for Children in the Pre-Hospital Environment | ||
| Medical condition: This research hopes to bridge the gap between in-hospital diamorphine and pre-hospital IV morphine by developing IN morphine for administration to children between 3 and 14 years old. This will all... | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-019180-10 | Sponsor Protocol Number: NCTU5248 | Start Date*: 2010-07-29 |
| Sponsor Name:The Newcastle upon Tyne Hospitals NHS Foundation Trust | ||
| Full Title: Paramedic Initiated Lisinopril For Acute Stroke Treatment(PIL-FAST): A Pilot Randomised Controlled Trial | ||
| Medical condition: Stroke and high blood pressure | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-004766-40 | Sponsor Protocol Number: 30592 | Start Date*: 2009-04-08 | |||||||||||
| Sponsor Name:University of Nottingham | |||||||||||||
| Full Title: Rapid Intervention with GTN in Hypertensive stroke Trial (RIGHT). Determining the potential of ambulance-based randomised controlled trials in patients with hyperacute stroke; assessment of glycery... | |||||||||||||
| Medical condition: Hypertension in acute stroke | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-002671-26 | Sponsor Protocol Number: 9113 | Start Date*: 2017-12-19 | |||||||||||
| Sponsor Name:Isala | |||||||||||||
| Full Title: The effect of Opioids on P2Y12 Receptor Inhibition in patients with ST-Elevation Myocardial Infarction who are pre-treated with crushed Ticagrelor | |||||||||||||
| Medical condition: Acute Coronary syndrome | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-004890-15 | Sponsor Protocol Number: EU-C-001-II-01 | Start Date*: 2019-06-05 | |||||||||||
| Sponsor Name:Eustralis Pharmaceuticals Ltd. | |||||||||||||
| Full Title: A double-blind placebo-controlled study with an open-label pilot phase, assessing the efficacy, tolerability and safety of EU-C-001 in patients with moderate to severe traumatic brain injury | |||||||||||||
| Medical condition: Traumatic brain injury | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-003320-16 | Sponsor Protocol Number: CEL-03 | Start Date*: 2020-12-23 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:CeleCor Therapeutics, Inc. | ||||||||||||||||||||||||||||||||||||||
| Full Title: A Phase 3 prospective, blinded, randomized, placebo controlled, international multicenter study to assess the safety and efficacy of a single subcutaneous injection of zalunfiban in subjects with S... | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Subjects with documented STEMI, presenting with persistent ischemic chest pain (>10 minutes) and new ≥2 mm ST-segment elevation in 2 adjacent ECG leads, in whom the total duration of symptoms to di... | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: NL (Trial now transitioned) CZ (Trial now transitioned) HU (Trial now transitioned) FR (Trial now transitioned) RO (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||
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