- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
4 result(s) found for: Antitachycardia pacing.
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EudraCT Number: 2004-004799-35 | Sponsor Protocol Number: DRI5349 | Start Date*: 2005-05-25 | |||||||||||
Sponsor Name:Sanofi-aventis recherche and developpement | |||||||||||||
Full Title: Double blind placebo controlled dose ranging study of the efficacy and safety of SSR149744C 100 or 300 mg for the prevention of ventricular arrhythmia-triggered ICD interventions | |||||||||||||
Medical condition: Ventricular arrhythmia triggered ICD interventions | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004376-11 | Sponsor Protocol Number: AZM-MD-302 | Start Date*: 2012-05-15 | |||||||||||
Sponsor Name:Forest Research Institute, Inc. | |||||||||||||
Full Title: A Phase 3 Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study of the Effects of Once-Daily Oral Doses of 75 mg Azimilide Dihydrochloride on the Incidence of Cardiovascular Hospitalizat... | |||||||||||||
Medical condition: Ventricular arrhythmia in patients with implantable cardioverter-defibrillator (ICD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Prematurely Ended) NL (Prematurely Ended) ES (Prematurely Ended) DE (Prematurely Ended) SE (Prematurely Ended) CZ (Prematurely Ended) DK (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004954-33 | Sponsor Protocol Number: 7U/2014 | Start Date*: 2014-11-27 | |||||||||||
Sponsor Name:Central Finland Hospital District | |||||||||||||
Full Title: Medical ANtiarrhythmic Treatment or Radiofrequency Ablation in ischemic Ventricular Tachyarrhythmias. A prospective, randomized multicentre study MANTRA-VT | |||||||||||||
Medical condition: Ventricular tachyarrhtyhmias in patients with prior myocardial infarction and implantable cardioverter defibrillator | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004430-15 | Sponsor Protocol Number: GS-US-356-0101 | Start Date*: 2014-10-07 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Phase 2, Double-Blind, Randomized, Placebo Controlled, Dose Ranging, Parallel Group Study to Evaluate the Effect of GS-6615 on Ventricular Arrhythmia in Subjects with Implantable Cardioverter-Def... | |||||||||||||
Medical condition: Subjects with an ICD or CRT-D implanted for primary or secondary prevention | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) PL (Completed) DK (Completed) CZ (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
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