- Trials with a EudraCT protocol (49)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
49 result(s) found for: Congenital malformations.
Displaying page 1 of 3.
EudraCT Number: 2011-001455-37 | Sponsor Protocol Number: 1331TMF | Start Date*: 2011-12-21 | |||||||||||
Sponsor Name:Department of Radiology, Oslo University Hospital, Norway | |||||||||||||
Full Title: Prospective randomized interventional study. Compare the effect of bleomycin and Tetradecyl Sodium Sulphate (Fibrovein) in the treatment of venous malformations. Clinical neurological and neurophys... | |||||||||||||
Medical condition: Venous malformation | |||||||||||||
|
|||||||||||||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) | |||||||||||||
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... | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Infants and toddlers, Children, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000321-69 | Sponsor Protocol Number: PHRCN10-Pr.DEVAUCHELLE | Start Date*: 2014-03-06 | |||||||||||
Sponsor Name:CHU Amiens | |||||||||||||
Full Title: Evaluation prospective de l’efficacité du sirolimus (Rapamune) dans le traitement des malformations artério-veineuses superficielles | |||||||||||||
Medical condition: Malformations artério-veineuses superficielles | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019713-21 | Sponsor Protocol Number: CS/2007/2678 | Start Date*: 2010-06-17 | ||||||||||||||||||||||||||
Sponsor Name:University Hospitals Bristol NHS Foundation Trust | ||||||||||||||||||||||||||||
Full Title: A RANDOMISED CONTROLLED TRIAL TO COMPARE NORMOXIC VERSUS STANDARD CARDIOPULMONARY BYPASS IN CYANOTIC CHILDREN UNDERGOING CARDIAC SURGERY | ||||||||||||||||||||||||||||
Medical condition: The study investigates reoxygenation injury in cyanotic paediatric patients undergoing on-pump cardiac surgery. The types of heart condition being investigated result in chronic low blood oxygen sa... | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-001096-43 | Sponsor Protocol Number: PHRN14-AM/PERFORMUS | Start Date*: 2015-07-10 | |||||||||||
Sponsor Name:CHRU de Tours | |||||||||||||
Full Title: Treatment of superficial voluminous complicated slow-flow vascular malformations with sirolimus: a phase 2 trial in children observational-phase designed | |||||||||||||
Medical condition: vascular malformations | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004322-28 | Sponsor Protocol Number: P120910 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
|
|||||||||||||
Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
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 | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004981-16 | Sponsor Protocol Number: 1991-201-008 | Start Date*: 2022-06-17 | |||||||||||
Sponsor Name:Editas Medicine, Inc. | |||||||||||||
Full Title: Open-Label, Single Ascending Dose Study to Evaluate the Safety, Tolerability, and Efficacy of EDIT-101 in Adult and Pediatric Participants with Leber Congenital Amaurosis Type 10 (LCA10), with Cen... | |||||||||||||
Medical condition: Leber Congenital Amaurosis Type 10 (LCA10), with Centrosomal Protein 290 (CEP290)-Related Retinal Degeneration Caused by a Compound Heterozygous or Homozygous Mutation Involving c.2991+1655A>G in I... | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-017978-21 | Sponsor Protocol Number: EMR700568-012 | Start Date*: 2010-12-20 | |||||||||||
Sponsor Name:Merck Serono S.A. - Geneva | |||||||||||||
Full Title: Prospective observational long-term safety registry of Multiple Sclerosis patients who have participated in cladribine clinical trials (PREMIERE) | |||||||||||||
Medical condition: Multiple Sclerosis patients who have participated in cladribine tablets clinical trials | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FI (Completed) LT (Completed) AT (Completed) GR (Completed) CZ (Completed) GB (Completed) EE (Completed) LV (Completed) BE (Completed) SE (Completed) PT (Completed) DK (Completed) ES (Completed) IT (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-001530-33 | Sponsor Protocol Number: DR190041 | Start Date*: 2019-06-29 | |||||||||||
Sponsor Name:CHRU TOURS | |||||||||||||
Full Title: TOPical sirolimus in linGUal microkystic lymphatic malformation-TOPGUN | |||||||||||||
Medical condition: Lingual microcystic lymphatic malformations (LMLM) in children and adults | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011276-29 | Sponsor Protocol Number: L00122 GI 201 (ORF) | Start Date*: 2009-08-21 |
Sponsor Name:ORFAGEN | ||
Full Title: Systemic and local diffusion of ethanol after administration of ethanol 96% formulated in a gel (L0122 Gel) and ethanol 98% solution (absolute ethanol) by the percutaneous route, in patients with c... | ||
Medical condition: patients with congenital venous malformations (CVM) | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-003812-23 | Sponsor Protocol Number: 107014 | Start Date*: 2006-12-21 |
Sponsor Name:NV Organon | ||
Full Title: Pregnancy and neonatal follow-up of ongoing pregnancies established after controlled ovarian stimulation in clinical trial 107012 for the development of Org 36286 (corifollitropin alfa) | ||
Medical condition: Controlled Ovarian Stimulation (COS) to induce the development of multiple follicles in patients participating in an Assisted Reproductive Technology (ART) program | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: SE (Completed) AT (Completed) CZ (Completed) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002800-15 | Sponsor Protocol Number: 2012_67 | Start Date*: 2015-10-13 | |||||||||||
Sponsor Name:Centre Hospitalier Régional Universitaire Lille | |||||||||||||
Full Title: Efficacy of Rapamycine (Sirolimus) in poor prognosis cervifo-facial lymphatic malformations | |||||||||||||
Medical condition: | |||||||||||||
|
|||||||||||||
Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
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. | |||||||||||||
|
|||||||||||||
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: 2009-017823-24 | Sponsor Protocol Number: 1703 | Start Date*: 2010-03-19 |
Sponsor Name:Tartu University Hospital | ||
Full Title: Meropenem pharmacokinetics in very low birth weight neonates | ||
Medical condition: proven or suspected sepsis, lower respiratory tract infection, complicated intraabdominal infection | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: EE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-003595-30 | Sponsor Protocol Number: IRFMN-7358 | Start Date*: 2018-02-21 | |||||||||||
Sponsor Name:IRCCS- ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI | |||||||||||||
Full Title: Treat_CCM Clinical Trial. A multicenter randomized clinical trial on Propranolol in Cerebral Cavernous Malformation | |||||||||||||
Medical condition: Cerebral Cavernous Malformation (CCM) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005419-18 | Sponsor Protocol Number: 01INMUNOGEST14 | Start Date*: 2016-07-01 | |||||||||||
Sponsor Name:silvia sanchez ramon | |||||||||||||
Full Title: CLINICAL TRIAL, PHASE III, RANDOMIZED, DOUBLE-BLIND PLACEBO-CONTROLLED WITH INTRAVENOUS IMMUNOGLOBULIN HUMAN FOR THE TREATMENT OF REPEAT ABORTION WITH IMMUNE ETIOLOGY | |||||||||||||
Medical condition: recurrent aborption with inmunological etiology | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002357-35 | Sponsor Protocol Number: SQ147214 | Start Date*: 2015-09-22 |
Sponsor Name:Research, Development & Innovation Department, UHCW NHS Trust | ||
Full Title: Anticoagulants for Living FoEtuses in women with recurrent miscarriage and inherited thrombophilia : ALIFE 2 | ||
Medical condition: Inherited thrombophilia in recurrent miscarriage | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: View results |
EudraCT Number: 2015-002506-37 | Sponsor Protocol Number: SANNI-project:03 | Start Date*: 2020-01-08 |
Sponsor Name:Region Skane | ||
Full Title: Dexmedetomidine for analgosedation to newborn infants during neonatal intensive care – a prospective pharmacokinetic/ pharmacodynamic/ pharmacogenetic observational study.Cohort 3 in The SANNI Pr... | ||
Medical condition: Sick newborn infants in need of intensive care. | ||
Disease: | ||
Population Age: Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-001031-39 | Sponsor Protocol Number: 69HCL17_0018 | Start Date*: 2017-05-19 | |||||||||||
Sponsor Name:Hospices Civils de Lyon | |||||||||||||
Full Title: BABH Study: Efficacy and safety of bevacizumab on severe bleedings associated with Hemorrhagic Hereditary Telangiectasia (HHT). A National, randomized multicenter phase III study. | |||||||||||||
Medical condition: Hemorrhagic Hereditary Telangiectasia | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
