- Trials with a EudraCT protocol (4,469)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (9,983)
4,469 result(s) found.
Displaying page 6 of 224.
| EudraCT Number: 2009-017160-17 | Sponsor Protocol Number: ALGO-01 | Start Date*: 2010-02-24 | ||||||||||||||||
| Sponsor Name:ISTITUTI ORTOPEDICI RIZZOLI | ||||||||||||||||||
| Full Title: NSAID USED IN MESOTHERAPY VS NSAID INTRAMUSCOLAR INJECTION IN algodistrophy TREATMENT: A RANDOMIZED, CONTROLLED STUDY | ||||||||||||||||||
| Medical condition: SUFFERED FROM ALGODISTROPHY PATIENTS | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Ongoing) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2008-003824-51 | Sponsor Protocol Number: 112036 | Start Date*: 2009-08-14 |
| Sponsor Name:GlaxoSmithKline Biologicals | ||
| Full Title: A phase III, open, multi-centre, controlled study to evaluate the long-term antibody persistence at 2 years, 3 years and 4 years after a single dose of GlaxoSmithKline (GSK) Biologicals’ meningoco... | ||
| Medical condition: Healthy male and female children who completed the primary immunisation study MenACWY-TT-039 (109670) and were 12 to 23 months of age at the time of primary vaccination. | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-009871-36 | Sponsor Protocol Number: 140/540 | Start Date*: Information not available in EudraCT |
| Sponsor Name:Friedrich- Alexander- Universität Erlangen Nürnberg | ||
| Full Title: Effect and Safety of preventive Treatment with ACE-Inhibitor and Beta-Blocker on the onset of Left Ventricular Dysfunction in Duchenne Muscular Dystrophy | ||
| Medical condition: | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male | |
| Trial protocol: DE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-017837-23 | Sponsor Protocol Number: SXF-TRA-152 | Start Date*: 2010-09-27 | |||||||||||
| Sponsor Name:Yolanda de Diego Otero | |||||||||||||
| Full Title: Ensayo piloto fase II de tratamiento doble ciego, aleatorizado, de una vía cruzada, para investigar la efectividad y seguridad de la combinación de Ácido Ascórbico (vitamina C) y Tocoferol (vitamin... | |||||||||||||
| Medical condition: Sindrome X frágil. CIE12 : 759.83. enfermedad rara. ORPHA 908. OMIM NUMBER 300264 | |||||||||||||
|
|||||||||||||
| Population Age: Children, Adolescents, Under 18 | Gender: Male | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-022329-13 | Sponsor Protocol Number: 4791 | Start Date*: 2010-10-26 |
| Sponsor Name:Hôpitaux Universitaires de Strasbourg | ||
| Full Title: Etude de phase I associant la rapamycine et l’irinotecan dans toutes tumeurs solides réfractaires de l’enfant | ||
| Medical condition: Tumeurs solides réfractaires de l'enfant | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-021265-80 | Sponsor Protocol Number: PHRCNATHorsCancer2010-HC11-05 | Start Date*: 2010-10-18 | |||||||||||
| Sponsor Name:Centre Hospitalier Universitaire de Reims | |||||||||||||
| Full Title: Injections intradétrusoriennes de toxine botulique A chez l'enfant présentant un syndrome d'hyperactivité vésicale neurogène : essai thérapeutique contrôlé multicentrique de non infériorité entre d... | |||||||||||||
| Medical condition: Syndrome d'hyperactivité vésicale neurogène chez l'enfant | |||||||||||||
|
|||||||||||||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-010722-19 | Sponsor Protocol Number: BI71023_3001 | Start Date*: 2009-11-04 | |||||||||||
| Sponsor Name:CSL Behring LLC | |||||||||||||
| Full Title: A Prospective, Multicenter, Open-label, Phase 3b Study of Human Plasma-Derived Factor XIII Concentrate in Subjects with Congenital Factor XIII Deficiency Estudio prospectivo, multicéntrico, con et... | |||||||||||||
| Medical condition: Congenital Factor XIII deficiency Deficiencia congénita de factor XIII | |||||||||||||
|
|||||||||||||
| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-010737-47 | Sponsor Protocol Number: HSJD-RTB-QTIA | Start Date*: 2009-06-12 |
| Sponsor Name:HOSPITAL SANT JOAN DE DÉU | ||
| Full Title: Ensayo de fase II, no randomizado, abierto, unicéntrico, de quimioterapia intraarterial con melfalán para el tratamiento del retinoblastoma (RTB) en fase intraocular avanzada. Phase II trial, no... | ||
| Medical condition: RETINOBLASTOMA UNILATERAL AVANZADO ADVANCED INTRAOCULAR RETINOBLASTOMA | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-023057-11 | Sponsor Protocol Number: DC02/RUP/3/09 | Start Date*: 2011-02-09 | |||||||||||
| Sponsor Name:J. Uriach y Compañía, S.A. | |||||||||||||
| Full Title: Efficacy and safety of rupatadine solution in the treatment of Chronic Spontaneous Urticaria (CSU) in paediatric patients (2-11 years old). | |||||||||||||
| Medical condition: Treatment of Chronic Spontaneous Urticaria (CSU) in paediatric patients (2-11 years old). | |||||||||||||
|
|||||||||||||
| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-016797-32 | Sponsor Protocol Number: IGG_ev_003 | Start Date*: 2009-11-23 | |||||||||||
| Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
| Full Title: Phase 2/3, twelve-month, multicenter, intra-subjectcontrolled (retrospective-prospective), open-label, active-treatment study to evaluate the efficacy, safety, tolerability and pharmacokinetics of ... | |||||||||||||
| Medical condition: secondary hyperparathyroidism in paediatric subjects with chronic kidney disease | |||||||||||||
|
|||||||||||||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-001844-34 | Sponsor Protocol Number: V03777 LE 301A | Start Date*: 2007-11-26 |
| Sponsor Name:Pierre Fabre Dermo-Cosmétique | ||
| Full Title: Non inferiority study of a malathion 0.5% lotion versus reference therapy in the treatment of head lice: multicentre, randomised, investigator masked, parallel group. | ||
| Medical condition: the patient who will be included in this clinical trial present a confirmed active head lice infestation. | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) BE (Completed) IT (Completed) EE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-000359-16 | Sponsor Protocol Number: VD-3 | Start Date*: 2007-04-16 |
| Sponsor Name:Ove Bäck, Dept Dermatology, University Hospital, Lund, Sweden | ||
| Full Title: Vitamin D and atopic allergy | ||
| Medical condition: Cumulative incidence of atopic allergy specified as atopic dermatitis, allergic asthma, and allergic rhinitis. Since IMP is a food supplement to protect from rickets we are looking at clinical sym... | ||
| Disease: | ||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
| Trial protocol: SE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2011-000407-41 | Sponsor Protocol Number: FSJD-ESCOKETA-2010 | Start Date*: 2011-07-01 | |||||||||||
| Sponsor Name:FUNDACIÓ SANT JOAN DE DEU | |||||||||||||
| Full Title: ASSESSMENT OF THE ANALGESIC EFFICACY AND TOLERABILITY OF THE PERIOPERATIVE ASSOCIATION OF KETAMINE WITH OPIATES AFTER POSTERIOR VERTEBRAL FUSION SURGERY IN CHILDREN WITH IDIOPATHIC SCOLIOSIS | |||||||||||||
| Medical condition: POSTERIOR VERTEBRAL FUSION SURGERY IN CHILDREN WITH IDIOPATHIC SCOLIOSIS | |||||||||||||
|
|||||||||||||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-005318-12 | Sponsor Protocol Number: NCTU:CONCEPT1 | Start Date*: 2012-04-13 | |||||||||||
| Sponsor Name:Newcastle upon Tyne Hospitals NHS Foundation Trust | |||||||||||||
| Full Title: Phase 1 study of use of 5% Carbogen in treatment of paediatric non-convulsive status epilepticus | |||||||||||||
| Medical condition: Paediatric non-convulsive status epilepticus | |||||||||||||
|
|||||||||||||
| Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-024253-36 | Sponsor Protocol Number: 10MI29 | Start Date*: 2012-08-03 | |||||||||||
| Sponsor Name:Great Ormond Street Hospital for Children NHS Trust | |||||||||||||
| Full Title: Phase I/II, historical controlled, open-label, non-randomised, single-centre trial to assess the safety and efficacy of EF1αS-ADA lentiviral vector mediated gene modification of autologus CD34+ cel... | |||||||||||||
| Medical condition: Adenosine deaminase (ADA) deficiency is an inherited disorder that damages the immune system and causes severe combined immunodeficiency (SCID). Children with SCID lack virtually all immune protect... | |||||||||||||
|
|||||||||||||
| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-023668-42 | Sponsor Protocol Number: CRI 102194 | Start Date*: 2011-02-03 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Southampton University Hospital NHS Trust | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: Pulmonary surfactant (S) biology in ventilated children on a paediatric intensive care unit with acute (A) hypoxic respiratory (R) failure- a pilot (P) study (S): (SARPS) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: acute hypoxic respiratory failure in children ventilated on paediatric intensive care | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2011-000476-34 | Sponsor Protocol Number: V59_40 | Start Date*: 2011-06-08 | ||||||||||||||||
| Sponsor Name:NOVARTIS VACCINES AND DIAGNOSTICS S.R.L. | ||||||||||||||||||
| Full Title: A Phase IV,PlaceboControlled,Randomized Study to Evaluate the Immunogenicity and Safety of a Combined Tetanus, Reduced Diphtheria Toxoid, Acellular Pertussis Vaccine (Tdap, Boostrix) and Quadrivale... | ||||||||||||||||||
| Medical condition: Menveo is indicated for active immunization of adolescents (from 11 years of age) and adults at risk of exposure to Neisseria meningitidis groups A, C, W135 and Y, to prevent invasive disease. | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2011-004742-18 | Sponsor Protocol Number: XM22-07 | Start Date*: 2012-04-04 |
| Sponsor Name:Merckle GmbH, a member of the ratiopharm group, a subsidiary of Teva Pharmaceutical Industries Ltd. Germany | ||
| Full Title: Multicenter, Open-label Study to Assess the Pharmacokinetics, Pharmacodynamics, Efficacy, Safety, Tolerability, and Immunogenicity of a Single, Subcutaneous Dose of 100μg/kg XM22 in 21 Children wit... | ||
| Medical condition: Children with Ewing Family of Tumors or Rhabdomyosarcoma receiving cytotoxic Chemotherapy for malignancy inducing neutropenia | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: HU (Completed) CZ (Completed) BG (Completed) PL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2009-015624-28 | Sponsor Protocol Number: GUI-LYM-AMI-01 | Start Date*: 2010-03-16 | |||||||||||
| Sponsor Name:Héctor Guiral Torner | |||||||||||||
| Full Title: Estudio doble ciego, aleatorizado, controlado con placebo, multicéntrico, de grupos paralelos para evaluar la eficacia de Lymphomyosot en la reducción de la incidencia de amigdalectomía en paciente... | |||||||||||||
| Medical condition: AMIGDALITIS CRÓNICA | |||||||||||||
|
|||||||||||||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-000595-32 | Sponsor Protocol Number: Ematonco/divmalinf/2006.1 | Start Date*: 2006-09-06 | |||||||||||
| Sponsor Name:ISTITUTO GIANNINA GASLINI | |||||||||||||
| Full Title: Rescue therapy for indwelling central venous Hickmann-Broviac catheter related infections with antibiotic lock technique | |||||||||||||
| Medical condition: Patients with Hemato-oncologic disease or undergoing Hematopoietic stem cell transplantation | |||||||||||||
|
|||||||||||||
| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (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
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
| 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. | |
Query did not match any studies.