- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
4 result(s) found for: Premature ventricular contraction.
Displaying page 1 of 1.
| EudraCT Number: 2021-002487-46 | Sponsor Protocol Number: APHP180618 | Start Date*: 2023-03-14 | |||||||||||
| Sponsor Name:Assistance Publique - Hôpitaux de Paris | |||||||||||||
| Full Title: Prophylactic frequent premature ventricular complexeS sUPPression on left ventriculaR function impairmEnt in aSymptomatic patientS SUPPRESS | |||||||||||||
| Medical condition: Premature ventricular contractions (PVCs) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-005688-36 | Sponsor Protocol Number: SCIVF2021 | Start Date*: 2022-09-19 |
| Sponsor Name:Amsterdam UMC | ||
| Full Title: Quinidine versus verapamil in short-coupled idiopathic ventricular fibrillation: An open label, randomized crossover pilot trial | ||
| Medical condition: Short-coupled idiopathic ventricular fibrillation is a rare syndrome and subtype of idiopathic ventricular fibrillation that is characterized by ventricular fibrillation or polymorphic ventricular ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-003670-25 | Sponsor Protocol Number: CQVA149A2203 | Start Date*: 2007-12-19 | |||||||||||
| Sponsor Name:Novartis Pharma AG | |||||||||||||
| Full Title: A randomized, double blind, placebo controlled, multicenter study to determine the effect of QVA149 on mean 24-hours heart rate in patients with Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
| Medical condition: Chronic Obstructive Pulmonary Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) DE (Completed) IT (Completed) BE (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-005671-92 | Sponsor Protocol Number: PT010005 | Start Date*: 2015-11-03 | ||||||||||||||||
| Sponsor Name:Pearl Therapeutics, Inc. | ||||||||||||||||||
| Full Title: A Randomized, Double Blind, Multi Center, Parallel Group Study to Assess the Efficacy and Safety of PT010 Relative to PT003 and PT009 on COPD Exacerbations over a 52 Week Treatment Period in Subjec... | ||||||||||||||||||
| Medical condition: Moderate to Very Severe Chronic Obstructive Pulmonary Disease (COPD) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) AT (Completed) DE (Completed) BE (Completed) PL (Completed) HU (Completed) CZ (Completed) SE (Completed) ES (Completed) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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