- Trials with a EudraCT protocol (59)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
59 result(s) found for: Heart beat.
Displaying page 1 of 3.
EudraCT Number: 2010-019442-87 | Sponsor Protocol Number: DROPPAF | Start Date*: 2010-07-02 |
Sponsor Name:East Sussex NHS Trust | ||
Full Title: Dronedarone in pacemaker patients with paroxysmal atrial fibrillation | ||
Medical condition: Paroxysmal atrial fibrillation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
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: 2016-002367-34 | Sponsor Protocol Number: 29052016 | Start Date*: 2016-09-30 | |||||||||||
Sponsor Name:Hjertemedicinsk klinik, Rigshospitalet | |||||||||||||
Full Title: Beta 3 agonist treatment in heart failure (BEAT-HF II) | |||||||||||||
Medical condition: Heart Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023495-11 | Sponsor Protocol Number: 2010-023495-11 | Start Date*: 2010-12-17 | |||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
Full Title: Esmolol to treat tachicardia in septic shock | |||||||||||||
Medical condition: septic shock | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002060-17 | Sponsor Protocol Number: 2015/077/HP | Start Date*: 2015-08-21 | |||||||||||||||||||||
Sponsor Name:CHU - Hôpitaux de Rouen | |||||||||||||||||||||||
Full Title: Effect of pharmacological heart rate reduction on visco-elastic properties of the arterial wall - Impact of aging | |||||||||||||||||||||||
Medical condition: Healthy subjects between 25 and 65 years old | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004456-38 | Sponsor Protocol Number: XEN-D0103-CL-05 | Start Date*: 2014-04-11 | |||||||||||
Sponsor Name:Xention Limited | |||||||||||||
Full Title: A double blind, randomised, placebo-controlled, crossover study assessing the use of XEN D0103 in patients with paroxysmal atrial fibrillation and implanted pacemakers allowing continuous beat-to-b... | |||||||||||||
Medical condition: Paroxysmal atrial fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-003703-21 | Sponsor Protocol Number: 5802003 | Start Date*: 2005-01-28 |
Sponsor Name:Semmelweis University | ||
Full Title: The role of hyperhomocysteinemia in the genesis of atherothrombotic vascular disease | ||
Medical condition: Established cardiovascular disease with elevated levels of homocystein | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002254-40 | Sponsor Protocol Number: 14-OBE001-013 | Start Date*: 2014-09-22 | |||||||||||
Sponsor Name:ObsEva SA | |||||||||||||
Full Title: A phase 2, double-blind, dose-finding, placebo-controlled study to assess the safety and efficacy of a single oral administration of OBE001 to improve embryo implantation following IVF or ICSI. | |||||||||||||
Medical condition: Embryo implantation in women undergoing embyo transfer following IVF/ICSI in the context of Assisted Reproductive Technology (ART). | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) BE (Completed) DK (Completed) CZ (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004805-29 | Sponsor Protocol Number: 201200480529 | Start Date*: 2013-06-04 | |||||||||||
Sponsor Name:The Heart Center, Rigshospitalet | |||||||||||||
Full Title: Beta 3 agonist treatment in heart failure (BEAT-HF) | |||||||||||||
Medical condition: Systolic heart failure | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001840-37 | Sponsor Protocol Number: 2017-001840-37 | Start Date*: 2019-01-15 |
Sponsor Name:VU University Medical Center | ||
Full Title: ERtugliflozin triAl in DIabetes with preserved or reduced ejeCtion FrAcTion mEchanistic evaluation in Heart Failure: "ERADICATE-HF" | ||
Medical condition: Diabetes Mellitus Type 2 and Heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001014-15 | Sponsor Protocol Number: S61372 | Start Date*: 2018-06-26 |
Sponsor Name:university hospital leuven | ||
Full Title: Frozen-thawed embryo transfer in a natural versus artificial cycle: a randomized clinical trial | ||
Medical condition: Patients with subfertility having frozen embryos after in vitro fertilization (IVF) or intracytoplasmatic sperm injection (ICSI) | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: BE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2015-001321-17 | Sponsor Protocol Number: 11275 | Start Date*: 2016-12-02 | ||||||||||||||||||||||||||
Sponsor Name:University of Oxford | ||||||||||||||||||||||||||||
Full Title: A randomised control trial of 5-Aminolevulinic Acid in combination with Sodium Ferrous Citrate to Enhance Cardioprotection in Adults undergoing Cardiac Surgery | ||||||||||||||||||||||||||||
Medical condition: Low cardiac output states following cardioplegic arrest for cardiac surgery | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003818-24 | Sponsor Protocol Number: DC2015RED01 | Start Date*: 2015-12-11 |
Sponsor Name:VU University Medical Center | ||
Full Title: A phase 4, monocenter, randomized, double-blind, comparator-controlled, parallel-group, mechanistic intervention trial to assess the effect of 12-week treatment with the sodium-glucose linked trans... | ||
Medical condition: Type 2 Diabetes Mellitus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001830-32 | Sponsor Protocol Number: RC31/17/0448 | Start Date*: 2019-12-18 |
Sponsor Name:University Hospital Toulouse | ||
Full Title: Phase III Trial to assess impact of ultra-long versus long down-regulation protocol on IVF/ICSI outcomes in infertile women presenting with adenomyosis. | ||
Medical condition: Infertilty in women with adenomyosis. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-001785-14 | Sponsor Protocol Number: STRESS-L | Start Date*: 2017-11-09 | ||||||||||||||||
Sponsor Name:University Hospitals Birmingham NHS Foundation Trust | ||||||||||||||||||
Full Title: STRESS-L: STudy into the REversal of Septic Shock with Landiolol (Beta Blockade) | ||||||||||||||||||
Medical condition: Tachycardia in Septic Shock | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000269-27 | Sponsor Protocol Number: DSCK101 | Start Date*: 2014-11-06 |
Sponsor Name:German Foundation for Chronically Ill | ||
Full Title: Efficacy and tolerance of Beta Blocker and Procoralan uptitration in chronic heart failure patients under telemedical control: „70 bpm on day 28“ | ||
Medical condition: Patients with chronic heart failure and resting heart rate of ≥ 75 bmp | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-002138-22 | Sponsor Protocol Number: LDLL300.401 | Start Date*: 2017-09-15 | ||||||||||||||||
Sponsor Name:AOP Orphan Pharmaceuticals GmbH | ||||||||||||||||||
Full Title: Phase IV, multicenter, prospective, randomized, open-label, controlled study on Landiolol in patients with septic shock resident in ICUs | ||||||||||||||||||
Medical condition: Adult patients in ICU with septic shock who remain tachycardic (HR ≥95 bpm) and require vasopressor therapy to maintain a Mean arterial pressure (MAP) of ≥65 mmHg after a hemodynamic optimization p... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) DE (Completed) CZ (Completed) SI (Completed) HU (Completed) LT (Completed) PL (Completed) EE (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-001547-12 | Sponsor Protocol Number: DC2017RACELINES01 | Start Date*: 2017-12-21 |
Sponsor Name:VU University Medical Center | ||
Full Title: A phase 4, monocenter, randomized, double-blind, comparator-controlled, 3-armed parallel mechanistic intervention trial to assess the effect of 8-week empagliflozin (SGLT-2 inhibitor) monotherapy, ... | ||
Medical condition: Type 2 Diabetes Mellitus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001622-10 | Sponsor Protocol Number: 000048 | Start Date*: 2012-10-08 | |||||||||||
Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
Full Title: A randomised, placebo-controlled, double-blind, parallel groups, multinational, multicentre trial assessing the effect of barusiban administered subcutaneously on the day of transfer on implantatio... | |||||||||||||
Medical condition: Infertility female | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Completed) ES (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004266-25 | Sponsor Protocol Number: 16-OBE001-005 | Start Date*: 2017-02-24 | |||||||||||
Sponsor Name:ObsEva S.A. | |||||||||||||
Full Title: A phase 3, double-blind, randomized, placebo-controlled study to assess the safety and efficacy of a single oral administration of nolasiban to improve pregnancy rates following IVF or ICSI in Day ... | |||||||||||||
Medical condition: Embryo implantation in women undergoing IVF or ICSI with Day 3 or Day 5 fresh embryo transfer cycles, in the context of Assisted Reproductive Technology (ART). | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: CZ (Completed) DE (Completed) DK (Completed) BE (Completed) HU (Completed) EE (Completed) ES (Completed) FI (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
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