- Trials with a EudraCT protocol (1,623)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (7)
1,623 result(s) found for: E site.
Displaying page 1 of 82.
EudraCT Number: 2011-001251-37 | Sponsor Protocol Number: 2011-011 | Start Date*: 2011-04-20 | |||||||||||
Sponsor Name:Vu Medical center | |||||||||||||
Full Title: Exploring alternative wound care treatment for percutanous gastrostomy site infection: a prospective, randomized, open, blinded end-point (PROBE) design. | |||||||||||||
Medical condition: Infection of the PEG(percutanous endoscopic gastrostomy)-insertion site. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003227-11 | Sponsor Protocol Number: DUR001-106 | Start Date*: 2014-11-28 | ||||||||||||||||
Sponsor Name:Durata Therapeutics International B.V. | ||||||||||||||||||
Full Title: PHASE 1, OPEN LABEL, SINGLE DOSE STUDY TO INVESTIGATE THE PHARMACOKINETICS, SAFETY AND TOLERABILITY OF DALBAVANCIN IN HOSPITALIZED CHILDREN AGED 3 MONTHS TO 11 YEARS RECEIVING STANDARD INTRAVENOUS ... | ||||||||||||||||||
Medical condition: Bacterial Infection in hospitalized children | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: EE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004709-17 | Sponsor Protocol Number: MP_SM01_2013 | Start Date*: 2014-02-10 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: Effect of High-dose Naloxone Infusion on Pain and Hyperalgesia in Inguinal Post-herniotomy Patients – A Randomized, Placebo-controlled, Double-blind Study | |||||||||||||
Medical condition: First degree burn injury in healthy volunteers who 6-8 weeks prior have had done a Inguinal herniotomy . | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022270-14 | Sponsor Protocol Number: 20101116 | Start Date*: 2011-02-11 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: Estudio abierto de extensión de fase 2 con conatumumab . A Phase 2 Open Label Extension Study of Conatumumab. | |||||||||||||
Medical condition: diferentes tumores sólidos, incluyendo, entre otros, cáncer colorrectal (CCR), cáncer de pulmón de células no pequeñas (CPCNP), sarcoma de tejidos blandos (STB), linfoma no Hodgkin (LNH), cáncer de... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014387-20 | Sponsor Protocol Number: DORI-PED-1003 | Start Date*: 2009-10-23 | |||||||||||
Sponsor Name:Janssen-Cilag International NV, Turnhoutseweg 30, 2340 Beerse, Belgium | |||||||||||||
Full Title: An Open-Label Study to Evaluate the Single-Dose Pharmacokinetics, Safety, and Tolerability of Doripenem in Infants (Term and Preterm), Less Than 12 Weeks Chronological Age Protocol DORI-PED-1003;... | |||||||||||||
Medical condition: hospitalized but medically stable infants (term and preterm), <12 weeks CA, who have documented, presumed to have, or are at risk for bacterial infection(s) and are undergoing treatment with i.v. a... | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (Completed) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001901-81 | Sponsor Protocol Number: AISAR-01-04 | Start Date*: 2004-07-23 | |||||||||||
Sponsor Name:AISAR ASSOCIAZIONE ITALIANA PER LO STUDIO DEGLI ANTIMICROBICI E DELLE RESISTENZE | |||||||||||||
Full Title: Efficacy and tollerability of thiamphenicol glycinate acetylcysteinate, given in sequential therapy sistematic and aerosol or by aerosol in the treatment of hight respiratory tract acute infectio... | |||||||||||||
Medical condition: terapia sequenziale sistemica ed aerosol delle infezioni acute e/o subacute/ricorrenti delle alte vie respiratorie | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006796-80 | Sponsor Protocol Number: TES10897 | Start Date*: 2009-04-23 | |||||||||||
Sponsor Name:Sanofi-Aventis Recherche & Développement | |||||||||||||
Full Title: The QUTIE Study: A Randomized, Double-Blind, Placebo-controlled Study Comparing Aflibercept Versus Placebo on the QTc interval in Cancer Patients treated with Docetaxel | |||||||||||||
Medical condition: Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) DK (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000466-33 | Sponsor Protocol Number: PT/11/2015 | Start Date*: 2016-03-22 | |||||||||||
Sponsor Name:Department of Pediatric oncology, Aarhus University hospital | |||||||||||||
Full Title: Pharmacokinetics and pharmacodynamics of Piperacillin-Tazobactam (PT) in pediatric oncology patients with fever and neutropenia. | |||||||||||||
Medical condition: Pediatric oncology patients with fever and neutropenia | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004749-41 | Sponsor Protocol Number: NEO-ONE | Start Date*: 2011-12-13 | |||||||||||
Sponsor Name:TweeSteden hospital | |||||||||||||
Full Title: The effects of neoadjuvant hormonal therapy on the course of PSA and testosterone in patients with low and intermediate-risk prostate carcinoma (NEO-ONE); A randomized controlled trial | |||||||||||||
Medical condition: Localized prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006411-20 | Sponsor Protocol Number: CHUBX 2008/20 | Start Date*: 2009-02-13 | |||||||||||
Sponsor Name:CHU de Bordeaux | |||||||||||||
Full Title: EVALUATION PRONOSTIQUE DE LA TOMOGRAPHIE PAR EMISSION DE POSITONS COUPLEE AU SCANNER (TEP-TDM) AU FLUOROMISONIDAZOLE MARQUE AU FLUOR 18 (18F-FMISO) DANS LES CANCERS EPIDERMOIDES DES VOIES AERODIGES... | |||||||||||||
Medical condition: CANCERS EPIDERMOIDES DES VOIES AERODIGESTIVES SUPERIEURES | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007241-12 | Sponsor Protocol Number: PH-L19SIPI131-07/07 | Start Date*: 2008-10-06 | |||||||||||
Sponsor Name:Philogen S.p.A. | |||||||||||||
Full Title: A PHASE I/II DOSE FINDING AND EFFICACY STUDY OF THE TUMOUR TARGETING HUMAN 131I-L19SIP MONOCLONAL ANTIBODY IN PATIENTS WITH CANCER | |||||||||||||
Medical condition: Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005238-19 | Sponsor Protocol Number: CD-2007-01 | Start Date*: 2007-07-26 | |||||||||||
Sponsor Name:Instituto Cientifico y Tecnologico de Navarra | |||||||||||||
Full Title: Estudio fase II con inmunoterapia mediante células dendríticas y linfocitos infiltrantes de tumor en tumores sólidos | |||||||||||||
Medical condition: Melanoma, renal cell carcinoma, hepatocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001359-60 | Sponsor Protocol Number: Vasobrain01 | Start Date*: 2015-06-16 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: Influence of vasopressors on brain oxygenation and microcirculation in anesthetized patients with cerebral tumors | |||||||||||||
Medical condition: Brain oxygenation and microcirculation under administration of Efedrin and Metaoxedrin in patients with cerebral tumor. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006449-14 | Sponsor Protocol Number: CHUBX2008/31 | Start Date*: 2009-02-13 | |||||||||||
Sponsor Name:CHU de Bordeaux | |||||||||||||
Full Title: Evaluation méthodologique de la tomographie par émission de positons couplée au scanner (TEP-TDM) au Fluoromisonidazole marqué au fluor 18 ([18F]-FMISO) dans l’évaluation de la réponse au traitemen... | |||||||||||||
Medical condition: Glioblastome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003257-29 | Sponsor Protocol Number: NL1208 | Start Date*: 2013-02-06 | |||||||||||
Sponsor Name:Reckitt Benckiser Healthcare (UK) | |||||||||||||
Full Title: A randomised, double-blind, multi-centre, placebo controlled parallel group study to evaluate the efficacy and tolerability of a new Ibuprofen patch in patients with acute sports related traumatic ... | |||||||||||||
Medical condition: Acute sports-related traumatic blunt soft tissue injury/contusion to the upper or lower limbs | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003544-37 | Sponsor Protocol Number: ABUHB/01/0816/1 | Start Date*: 2016-11-30 | ||||||||||||||||||||||||||
Sponsor Name:Aneurin Bevan University Health Board | ||||||||||||||||||||||||||||
Full Title: Perineural Local Anaesthetic Catheter aftEr Major lowEr limb amputatioN Trial (PLACEMENT) | ||||||||||||||||||||||||||||
Medical condition: Analgesia for lower limb amputation for peripheral vascular disease (PVD) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-000415-32 | Sponsor Protocol Number: DAL-PK-02 | Start Date*: 2022-06-07 | |||||||||||
Sponsor Name:Allergan | |||||||||||||
Full Title: Pharmacokinetics of a Single-Dose of Dalbavancin in Preterm Neonates to Infants Ages 3 Months With Suspected or Confirmed Bacterial Infection | |||||||||||||
Medical condition: Bacterial Infection in hospitalized children | |||||||||||||
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Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000888-16 | Sponsor Protocol Number: 16-001 | Start Date*: 2018-05-17 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Bronchoscopic indocyanine green fluorescence imaging for the evaluation of anastomotic healing after lung transplantation | ||
Medical condition: Anastomotic healing after lung transplantation | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-001725-10 | Sponsor Protocol Number: 13-001 | Start Date*: 2014-01-24 |
Sponsor Name:Medizinische Universität Wien | ||
Full Title: Bronchoscopic indocyanine green fluorescence imaging for the evaluation of tracheal perfusion after surgery | ||
Medical condition: Tracheal stenosis secondary to malign and benign conditions | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002546-36 | Sponsor Protocol Number: CAPS2 | Start Date*: 2013-10-01 | |||||||||||
Sponsor Name:Medizinische Universität Wien, Universitätsklinik für Anästhesie, Allgemeine Intensivmedizin und Schmerztherapie | |||||||||||||
Full Title: Heat-, Cold-, and Mechanical Painthresholds under exposition of high dose topical Capsaicin | |||||||||||||
Medical condition: Pain | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
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