- Trials with a EudraCT protocol (4,033)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4,787)
4,033 result(s) found for: children.
Displaying page 1 of 202.
| EudraCT Number: 2008-001071-30 | Sponsor Protocol Number: V1 | Start Date*: 2010-01-21 |
| Sponsor Name:Medical University Vienna- Dept. of Pediatric Hemostaselology | ||
| Full Title: Aspirin Resistance in Children after Interventional Cardiac Catheterization: The ARC Study | ||
| Medical condition: children after interventional cardiac catheterization. | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-000606-11 | Sponsor Protocol Number: 5502071979 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Region Ostergotland | ||
| Full Title: Melatonin compared to sleep deprivation for sleep EEG recordings in children: impact on epileptiform discharges and sleep, contributing factors on the results and the influence on children's and pa... | ||
| Medical condition: suspected epilepsy | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-001735-37 | Sponsor Protocol Number: FL-CR001 | Start Date*: 2006-02-16 |
| Sponsor Name:FERRING ARZNEIMITTEL Ges.m.b.h. CEE AUSTRIA | ||
| Full Title: AN OPEN LABEL STUDY OF ORAL DESMOPRESSIN IN CHILDREN AGED 5 TO 15 YEARS WITH PRIMARY NOCTURAL ENURESIS | ||
| Medical condition: Primary noctural enuresis | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: SI (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2020-001769-35 | Sponsor Protocol Number: OYS042020. | Start Date*: Information not available in EudraCT |
| Sponsor Name:Oulu University Hopsital | ||
| Full Title: Preventing urinary tract infections in infants and young children with probiotic E. coli Nissle: FinNiss- trial | ||
| Medical condition: Urinary tract infection | ||
| Disease: | ||
| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: FI (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-000379-96 | Sponsor Protocol Number: INnaloxonePed-1 | Start Date*: 2017-05-05 |
| Sponsor Name:Karolinska University Hospital | ||
| Full Title: Pharmacokinetic and pharmacodynamic aspects in children after intranasal administration of the opioid antagonist naloxone | ||
| Medical condition: Pharmacokinetic profile after nasal naloxone administration in Children. In second part study reversal of sedation after opioid use | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-004958-34 | Sponsor Protocol Number: UNOLE0457 | Start Date*: 2015-01-30 |
| Sponsor Name:University of Leicester | ||
| Full Title: Midazolam Measurement and Modelling using Matrix Samplers | ||
| Medical condition: Not applicable | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-002094-55 | Sponsor Protocol Number: 1861 | Start Date*: 2019-09-09 |
| Sponsor Name:Universitair Ziekenhuis Brussel, Belgium | ||
| Full Title: Safety and feasibility of S-Caine patch use in children under the age of three | ||
| Medical condition: children under the age of three that are in possession of a central catheter and under permanent monitoring (healthy, or any condition) | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: BE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-006736-22 | Sponsor Protocol Number: NAF 03.4.05.033 | Start Date*: 2007-02-14 |
| Sponsor Name:Netherlands Asthma Foundation (NAF) [...] | ||
| Full Title: An early diagnosis of asthma in young children by using non-invasive biomarkers of oxidative stress/airway inflammation, and early lung function measurements | ||
| Medical condition: children with recurrent respiratory symptoms) | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Not Authorised) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2013-002273-22 | Sponsor Protocol Number: 1/2013 | Start Date*: 2013-07-24 |
| Sponsor Name:Azienda Ospedaliera L. Sacco - Clinica Pediatrica | ||
| Full Title: Efficacy of Pidotimod in the prevention of respiratory infections in healthy children: a randomized, double blind, placebo controlled study. | ||
| Medical condition: respiratory infections in children. | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2016-002601-19 | Sponsor Protocol Number: OND-URG | Start Date*: 2019-09-16 |
| Sponsor Name:Basque Health Service | ||
| Full Title: Effectiviness and safety of the administration of ondansetron versus placebo for the treatment of vomit in children with mild and moderate dehydration: randomized clinical trial | ||
| Medical condition: Vomiting | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2007-001817-40 | Sponsor Protocol Number: NAF 3.4.05.003 | Start Date*: 2007-05-10 |
| Sponsor Name:Netherlands Asthma Foundation (NAF) [...] | ||
| Full Title: An early diagnosis of asthma in young children by using non-invasive biomarkers of oxidative stress/airway inflammation | ||
| Medical condition: young children with recurrent respiratory symptoms | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-001938-96 | Sponsor Protocol Number: PGLIT2016 | Start Date*: 2016-12-22 |
| Sponsor Name:Helsinki University Central Hospital | ||
| Full Title: Treatment of Giardia lamblia infections in children: randomized open-labeled trial comparing rectal metronidazole with oral tinidazole | ||
| Medical condition: Symptomatic Giardia lamblia infections in children | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: FI (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-002925-29 | Sponsor Protocol Number: 200605 | Start Date*: 2005-09-20 |
| Sponsor Name:University Childrens Hospital | ||
| Full Title: Irinotecan singele drug treatment for children with refractory or relapsed hepatoblastoma | ||
| Medical condition: Refractory or recurrent hepatoblastoma | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-022655-29 | Sponsor Protocol Number: RATE-trial | Start Date*: 2011-05-30 |
| Sponsor Name:Erasmus MC | ||
| Full Title: Randomised open label cross-over study into the efficacy of RApamycin in children with Tuberous sclerosis complex with intractable Epilepsy (RATE-trial) | ||
| Medical condition: Epilepsy in children with Tuberous Sclerosis Complex | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-005016-93 | Sponsor Protocol Number: | Start Date*: 2005-04-01 |
| Sponsor Name:Vrinnevi Hospital | ||
| Full Title: Oral immunoglobulin - a novel treatment of children with Crohn´s disease | ||
| Medical condition: Children with the chronic inflammatory bowel Crohn´s disease in an active phase | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-006717-32 | Sponsor Protocol Number: 554 | Start Date*: 2007-01-31 |
| Sponsor Name:Stefan Lundeberg | ||
| Full Title: Pharmacokinetic study of the opioid ketobemidone in children and adolescens after intravenous administration | ||
| Medical condition: Pain treatment with opioids in children | ||
| Disease: | ||
| Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-002175-40 | Sponsor Protocol Number: no number | Start Date*: 2008-12-17 |
| Sponsor Name: | ||
| Full Title: Effect of Botulinum Toxin A Injections and Specific Intensive Rehabilitation Therapy in Children with Hemiparetic Cerebral Palsy on Upper Limb Functions and Skills | ||
| Medical condition: Study design: a factorial design with four study groups in which btA alone, intensive rehabilitation therapy aimed at improving bimanual skills alone, a combination of these two and continuing the ... | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-002323-28 | Sponsor Protocol Number: prop01 | Start Date*: 2016-06-28 |
| Sponsor Name:Universitair Ziekenhuis Brussel | ||
| Full Title: Blood concentration and pharmacokinetic analysis of propofol following administration of single induction dose in small children | ||
| Medical condition: Children scheduled for elective surgery | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: BE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-023976-16 | Sponsor Protocol Number: Matab2 | Start Date*: 2010-02-08 |
| Sponsor Name:University of Antwerp | ||
| Full Title: Maternal antibodies against pertussis in neonates . | ||
| Medical condition: Pertussis disease is reported in very young children who have not yet been (fully) vaccinated and did not receive sufficient maternal antibodies. Augmenting maternal antibody titers by administerin... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: BE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-023844-34 | Sponsor Protocol Number: ParCS | Start Date*: 2011-06-30 | |||||||||||
| Sponsor Name:Sint Maartenskliniek | |||||||||||||
| Full Title: Effectiveness and safety of parecoxib in children undergoing scoliosis surgery compared to placebo: a double-blinded randomised controlled trial | |||||||||||||
| Medical condition: Postoperative pain in children after scoliosis surgergy (spinal fusion). The morphine consumption on the first two postoperative days will be assessed. Children: <18 years old, ASA I or II | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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