- Trials with a EudraCT protocol (169)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
169 result(s) found for: Congenital cardiac disorders.
Displaying page 1 of 9.
| EudraCT Number: 2007-000390-31 | Sponsor Protocol Number: HyperHAES-PÄD-CARDIO-02 | Start Date*: 2007-10-30 | |||||||||||
| Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
| Full Title: Application of hypertonic hyperoncotic solutions for improvement of cardiac output after open heart surgery in children - monocentric, randomised, placebo controlled, double-blind clinical trial (p... | |||||||||||||
| Medical condition: Children after open-heart surgery for congenital cardiac disease | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-005239-14 | Sponsor Protocol Number: 062011 | Start Date*: 2012-01-05 | |||||||||||
| Sponsor Name:Pertti Suominen [...] | |||||||||||||
| Full Title: | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Newborns, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-000946-38 | Sponsor Protocol Number: EFC5314 | Start Date*: 2007-01-24 | |||||||||||
| Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
| Full Title: International randomized double blind clinical study evaluating the efficacy and safety of clopidogrel 0.2mg/kg once daily versus placebo in neonates and infants with cyanotic congenital heart dise... | |||||||||||||
| Medical condition: Neonates or infants (age less than or equal to 92 days at the time of randomization) with systemic to pulmonary arterial shunt for palliation of cyanotic congenital heart disease. | |||||||||||||
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| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) GB (Completed) DE (Completed) FI (Completed) SE (Completed) DK (Completed) PT (Completed) FR (Completed) HU (Completed) IT (Completed) NL (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-004596-31 | Sponsor Protocol Number: NL62772 | Start Date*: 2019-03-25 | ||||||||||||||||
| Sponsor Name:UMC Utrecht | ||||||||||||||||||
| Full Title: CeRebrUm and CardIac protection with Allopurinol in neonates with critical congenital heart disease requiring cardiac surgery with cardiopulmonary bypass | ||||||||||||||||||
| Medical condition: Brain injury in neonates with critical congenital heart disease requiring cardiac surgery with cardiopulmonary bypass. | ||||||||||||||||||
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| Population Age: Newborns, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2008-004999-53 | Sponsor Protocol Number: LTS10916 | Start Date*: 2009-02-06 | |||||||||||
| Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
| Full Title: Long-term safety study in patients included in CLARINET study with cyanotic congenital heart disease palliated with a systemic-to-pulmonary artery shunt and for whom the shunt is still in place at... | |||||||||||||
| Medical condition: Patients at one year of age who are included in CLARINET, with cyanotic congenital heart disease palliated with a systemic-to-pulmonary artery shunt, and for whom the shunt is still in place. | |||||||||||||
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| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: PT (Completed) HU (Completed) ES (Completed) BE (Completed) DE (Completed) FR (Completed) IT (Completed) GB (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-007042-18 | Sponsor Protocol Number: CHD Vasovist | Start Date*: 2007-03-08 | |||||||||||
| Sponsor Name:Kings College London [...] | |||||||||||||
| Full Title: Improved Diagnosis of Congenital Heart Disease by MRI using Vasovist - CHD Vasovist | |||||||||||||
| Medical condition: Congenital Heart Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-001784-77 | Sponsor Protocol Number: ML6721 | Start Date*: 2012-05-07 | |||||||||||
| Sponsor Name:University Hospitals Leuven | |||||||||||||
| Full Title: Fontan patients: Comprehensive evaluation of the pulmonary circulation to identify pulmonary vascular disease and its influence on ventricular hemodynamics. | |||||||||||||
| Medical condition: Fontan patients | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-007413-76 | Sponsor Protocol Number: steroiditutkimus | Start Date*: 2009-02-27 | |||||||||||
| Sponsor Name:Pertti Suominen | |||||||||||||
| Full Title: Metyyliprednisolonin farmakokinetiikka ja -dynamiikka lasten avosydänleikkausten yhteydessä | |||||||||||||
| Medical condition: Lasten ja nuorten sairaalassa (HUS) hoidettavat 1-12 kk ikäiset avosydänleikkaukseen tulevat potilaat, joilla on sydänvikanan TOF, AVSD tai VSD. Lasten ja nuorten sairaalassa (HUS) hoidettavat ko... | |||||||||||||
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| Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-001189-40 | Sponsor Protocol Number: 3 | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
| Sponsor Name:University of Tartu | ||||||||||||||||||||||||||||
| Full Title: PHARMACOKINETICS OF ORAL SPIRONOLACTONE IN CHILDREN UP TO 2 YEARS OF AGE | ||||||||||||||||||||||||||||
| Medical condition: cardiac failure, ascites and/or oedema | ||||||||||||||||||||||||||||
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| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: EE (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2012-004343-80 | Sponsor Protocol Number: 545.12 | Start Date*: 2012-09-20 | |||||||||||
| Sponsor Name:OSPEDALE PEDIATRICO BAMBINO GESU' DI ROMA | |||||||||||||
| Full Title: STUDY PHASE III, RANDOMIZED, DOUBLE-BLIND CONTROLLED TO EVALUATE THE EFFECTIVENESS OF FUROSEMIDE IN CONTINUOUS INFUSION VS ethacrynic acid IN CONTINUOUS INFUSION IN CHILDREN SUBJECT TO A heart sur... | |||||||||||||
| Medical condition: ALL CHILDREN AGE 'LESS THAN 10 YEARS OF AGE' WITH CONGENITAL HEART PROCEDURE SUBJECT TO cardiac surgery in whom the diuretic ARE GIVEN IN ACCORDANCE WITH THE FOLLOWING CONTINUOUS INFUSION PROTOCOL ... | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-002396-18 | Sponsor Protocol Number: 2015-602295-02 | Start Date*: 2015-11-30 | |||||||||||
| Sponsor Name:Ethicare GmbH | |||||||||||||
| Full Title: ORODISPERSIBLE MINITABLETS OF ENALAPRIL IN YOUNG CHILDREN WITH HEART FAILURE DUE TO CONGENITAL HEART DISEASE | |||||||||||||
| Medical condition: Heart Failure due to Congenital Heart Disease | |||||||||||||
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| Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) GB (Prematurely Ended) NL (Ongoing) AT (Completed) DE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-001247-39 | Sponsor Protocol Number: CV185-362 | Start Date*: 2017-04-24 | |||||||||||||||||||||||||||||||
| Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||||||||||||||||||||||
| Full Title: A Prospective, Randomized, Open Label, Multi-center Study of the Safety and Pharmacokinetics of Apixaban versus Vitamin K Antagonist or LMWH in Pediatric Subjects with Congenital or Acquired Heart ... | |||||||||||||||||||||||||||||||||
| Medical condition: Congenital or Acquired Heart Disease Requiring Chronic Anticoagulation for Thromboembolism Prevention | |||||||||||||||||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) IT (Completed) FI (Completed) AT (Completed) ES (Prematurely Ended) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2011-003325-10 | Sponsor Protocol Number: 1.01 | Start Date*: 2012-08-10 | |||||||||||||||||||||
| Sponsor Name:VU University Medical Center | |||||||||||||||||||||||
| Full Title: A randomized controlled trail on the effects of periconceptional and prenatal folic acid supplementation on congenital anomalies and preterm birth | |||||||||||||||||||||||
| Medical condition: congenital anomalies | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||||||||||||
| Trial protocol: NL (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2013-003532-68 | Sponsor Protocol Number: FIBCON | Start Date*: 2014-03-11 | ||||||||||||||||
| Sponsor Name:Guy's and St Thomas NHS Foundation Trust | ||||||||||||||||||
| Full Title: Fibrinogen concentrate supplementation in the management of bleeding during paediatric cardiopulmonary bypass: a phase 1B/2A, open label dose escalation study (Version 1.0, Jan 28, 2014) | ||||||||||||||||||
| Medical condition: Neonates and infants who are at risk of mediastinal bleeding following cardiopulmonary bypass surgery for congenital heart disease | ||||||||||||||||||
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| Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2009-010404-28 | Sponsor Protocol Number: G83627057 | Start Date*: 2009-06-12 | ||||||||||||||||
| Sponsor Name:Fundación de Investigación Biomédica del Hospital Universitario La Paz, Madrid | ||||||||||||||||||
| Full Title: PREVENCIÓN DEL SÍNDROME DE BAJO GASTO POSTOPERATORIO EN RECIÉN NACIDOS SOMETIDOS A CIRUGÍA CARDIOVASCULAR: ESTUDIO PILOTO SOBRE LA FARMACOCINÉTICA Y FARMACODINAMIA DOSIS-DEPENDIENTE DE DOS INODILA... | ||||||||||||||||||
| Medical condition: Este estudio evaluará la eficacia de dos inodilatadores (IND) en el tratamiento del síndrome de bajo gasto postoperatorio (SBGP) en recién nacidos sometidos a cirugía cardiovascular (CCV) | ||||||||||||||||||
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| Population Age: Newborns, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2013-002856-33 | Sponsor Protocol Number: ALN-TTRSC-002 | Start Date*: 2013-11-15 | |||||||||||
| Sponsor Name:Alnylam Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Phase 2, Open-Label Trial to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics and Exploratory Clinical Activity of ALN-TTRSC in Patients with Transthyretin (TTR) Cardiac Amyloidosis | |||||||||||||
| Medical condition: Transthyretin (TTR) Cardiac Amyloidosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-001229-34 | Sponsor Protocol Number: ALN-TTRSC-003 | Start Date*: 2014-08-01 | |||||||||||
| Sponsor Name:Alnylam Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Phase 2, Open-label Extension Study to Evaluate the Long-Term Safety, Clinical Activity, and Pharmacokinetics of ALN-TTRSC in Patients with Transthyretin (TTR) Cardiac Amyloidosis Who Have Previo... | |||||||||||||
| Medical condition: Transthyretin (TTR) Cardiac Amyloidosis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004068-74 | Sponsor Protocol Number: ZEPLAST-PED | Start Date*: 2019-09-26 | |||||||||||
| Sponsor Name:I.R.C.C.S. POLICLINICO SAN DONATO | |||||||||||||
| Full Title: ZEro_PLASma Trial in small infants undergoing cardiac surgery | |||||||||||||
| Medical condition: Congenital heart disease | |||||||||||||
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| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-002397-21 | Sponsor Protocol Number: 2015-602295-03 | Start Date*: 2015-11-30 | ||||||||||||||||
| Sponsor Name:Ethicare GmbH | ||||||||||||||||||
| Full Title: FOLLOW-UP SAFETY TRIAL IN CHILDREN WITH CHRONIC HEART FAILURE THERAPY RECEIVING ORODISPERSIBLE MINITABLETS OF ENALAPRIL | ||||||||||||||||||
| Medical condition: Heart Failure due to Dilated Cardiomyopathy and Congenital Heart Disease | ||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
| Trial protocol: HU (Completed) GB (GB - no longer in EU/EEA) NL (Ongoing) AT (Completed) DE (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2016-002157-38 | Sponsor Protocol Number: 57911 | Start Date*: 2017-09-14 | ||||||||||||||||||||||||||
| Sponsor Name:Radboud University Medical Center | ||||||||||||||||||||||||||||
| Full Title: Treatment of congenital vascular malformations using Sirolimus: improving quality of Life | ||||||||||||||||||||||||||||
| Medical condition: congenital vascular malformation : Vascular malformations can involve lymphatic vessels, capillaries, veins and arteries or even combinations. These vascular malformations are present at birth an... | ||||||||||||||||||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
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