- Trials with a EudraCT protocol (409)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (189)
409 result(s) found for: Observational study.
Displaying page 3 of 21.
EudraCT Number: 2015-005185-34 | Sponsor Protocol Number: IPV29 | Start Date*: 2015-11-19 |
Sponsor Name:Sanofi Pasteur China | ||
Full Title: Safety study of IMOVAX Polio in selected cities in China, an observational post marketing study | ||
Medical condition: Poliomyelitis | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2015-005186-23 | Sponsor Protocol Number: IPV34 | Start Date*: 2015-11-19 |
Sponsor Name:Sanofi Pasteur China | ||
Full Title: Large scale safety study of IMOVAX Polio in selected cities in China, an observational post marketing study | ||
Medical condition: Poliomyelitis | ||
Disease: | ||
Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2009-012876-29 | Sponsor Protocol Number: 10762 | Start Date*: 2009-07-07 |
Sponsor Name:University Hospitals Leicester | ||
Full Title: A prospective study to assess emergence and transmissibility of drug resistance to neuraminidase inhibitor following treatment of children and adults with acute pandemic influenza | ||
Medical condition: Influenza | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-002470-40 | Sponsor Protocol Number: PROSORA | Start Date*: 2017-11-16 |
Sponsor Name:Erasmus MC Cancer Institute | ||
Full Title: Observational study of the effects of probenecid on the pharmacokinetics and pharmacodynamics of sorafenib (PROSORA-study) | ||
Medical condition: patients with unresectable hepatocellular cancer, advanced clear-cell renal cell carcinoma, locally recurrent or metastatic, progressive, differentiated thyroid carcinoma refractory to radioactive ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-001369-28 | Sponsor Protocol Number: 880 | Start Date*: 2014-10-30 | |||||||||||
Sponsor Name:Gateshead Health NHS Foundation Trust | |||||||||||||
Full Title: THYRoxine in Acute Myocardial Infarction (ThyrAMI) | |||||||||||||
Medical condition: Hypothyroidism and Acute Myocardial Infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005101-21 | Sponsor Protocol Number: OXI3001 | Start Date*: 2009-03-20 |
Sponsor Name:Mundipharma Research Limited | ||
Full Title: An open, multi-centre, non-comparative observational study to assess the safety and tolerability of Oxycodone hydrochloride injection 50 mg/mL as a subcutaneous infusion in subjects with severe can... | ||
Medical condition: Severe cancer pain | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2021-003686-36 | Sponsor Protocol Number: AR13001 | Start Date*: 2021-07-19 |
Sponsor Name:Finnish Defence Forces | ||
Full Title: Immune response to SARS-CoV-2 vaccines and its clinical significance in the Finnish Defence Forces | ||
Medical condition: Immune response induced by SARS-CoV-2 vaccination. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001825-28 | Sponsor Protocol Number: R119513 | Start Date*: 2019-09-24 | |||||||||||
Sponsor Name: The University of Manchester | |||||||||||||
Full Title: Mesoangioblast-mediated exon 51 skipping for genetic correction of dystrophin, based upon a single injection in individual skeletal muscles of five non ambulant patients affected by Duchenne Muscul... | |||||||||||||
Medical condition: Duchenne Muscular Dystrophy | |||||||||||||
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Population Age: Adolescents, Under 18 | Gender: Male | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004370-28 | Sponsor Protocol Number: 11-03/FusBet-C | Start Date*: 2012-06-25 | |||||||||||
Sponsor Name:Dermapharm AG | |||||||||||||
Full Title: Double-blind, randomized clinical trial to compare the efficacy and safety of fusidic acid 2% betamethasone 0,1% cream vs. Fucicort cream vs. vehicle for patients with bacterial infected eczemas. | |||||||||||||
Medical condition: Bacterial infected eczemas | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-001309-22 | Sponsor Protocol Number: 2593957 | Start Date*: 2021-03-29 | |||||||||||
Sponsor Name:IQVIA Commercial GmbH & Co. OHG | |||||||||||||
Full Title: Evaluation of immunological effects of the hedgehog inhibitors on basal cell carcinoma - An open label, prospective, observational biomarker study of the DeCOG. | |||||||||||||
Medical condition: Basal cell carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000177-31 | Sponsor Protocol Number: CAN-004AB | Start Date*: 2012-10-18 | |||||||||||
Sponsor Name:Prima BioMed Ltd | |||||||||||||
Full Title: CANVAS: A Randomized Trial of Cvac (Autologous Dendritic Cells Pulsed with Recombinant Human Fusion Protein [Mucin 1-Glutathione S Transferase] Coupled to Oxidized Polymannose) as Maintenance Treat... | |||||||||||||
Medical condition: Maintenance Treatment in [A] Patients with Epithelial Ovarian Cancer (EOC) in Complete Remission Following First-Line Chemotherapy and [B] Patients with EOC in Second Remission | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: LT (Prematurely Ended) BG (Prematurely Ended) DE (Prematurely Ended) BE (Completed) LV (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000722-19 | Sponsor Protocol Number: M12-919 | Start Date*: 2016-10-24 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Multicenter, Single-Arm Study of the Effects of Atrasentan on Spermatogenesis and Testicular Function | |||||||||||||
Medical condition: Diabetic Nephropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022682-98 | Sponsor Protocol Number: NL33774.000.10 | Start Date*: 2010-10-14 |
Sponsor Name:Julius Center for Health Sciences and Primary Care, UMC Utrecht | ||
Full Title: Monitoring of influenza-like symptoms among elderly, an observational study | ||
Medical condition: influenza-like illness (ILI) lower respiratory tract infection (LRTI) | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-003594-28 | Sponsor Protocol Number: BCCT2011 | Start Date*: 2013-11-07 | ||||||||||||||||
Sponsor Name:BioTissue Technologies GmbH | ||||||||||||||||||
Full Title: A Comparative Observational Prospective Randomized Open-Label Study on Efficacy of BioSeed®-C and chondrotissue® Treatment of Local Femoral Cartilage Defects in the Knee. | ||||||||||||||||||
Medical condition: focal femoral cartilage defects in the knee joint | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004179-11 | Sponsor Protocol Number: 2018-4898 | Start Date*: 2019-06-03 |
Sponsor Name:Radboudumc | ||
Full Title: Effectiveness of Somatostatin Analogues in Patients with hereditary hemorrhagic telangiectasia and symptomatic gastrointestinal bleeding, the SAIPAN-trial: a multicenter, randomized, open-label, pa... | ||
Medical condition: Hereditary hemorrhagic telangiectasia (HHT) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) DE (Ongoing) FR (Completed) IT (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002470-20 | Sponsor Protocol Number: SANNI-project:01 | Start Date*: 2017-04-11 |
Sponsor Name:Skåne University Hospital | ||
Full Title: Fentanyl and Clonidine for analgesia during hypothermia in term asphyxiated infants – a prospective pharmacokinetic/ pharmacodynamic/ pharmacogenetic observational study. Cohort 1 in The SANNI proj... | ||
Medical condition: Infants with induced hypothermic treatment after perinatal asphyxia | ||
Disease: | ||
Population Age: Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-000630-34 | Sponsor Protocol Number: MLN0002-3029 | Start Date*: 2022-12-09 |
Sponsor Name:Takeda Development Center Americas, Inc. | ||
Full Title: A Phase 3b Extension Study to Evaluate the Long-term Safety of Vedolizumab Intravenous in Pediatric Patients With Ulcerative Colitis or Crohn’s Disease | ||
Medical condition: Active Ulcerative Colitis (UC) or Crohn's disease (CD) | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: HU (Trial now transitioned) PL (Trial now transitioned) CZ (Prematurely Ended) ES (Prematurely Ended) SK (Prematurely Ended) GR (Trial now transitioned) BE (Trial now transitioned) LT (Completed) HR (Trial now transitioned) Outside EU/EEA | ||
Trial results: (No results available) |
EudraCT Number: 2005-002534-35 | Sponsor Protocol Number: 15022288 | Start Date*: 2005-09-14 |
Sponsor Name:Coombe Women's Hospital | ||
Full Title: Determination of plasma concentration of levobupivicaine following low concentration epidural infusion of levobupivicaine in pre-eclamptic and non pre-eclamptic nulliparous women. | ||
Medical condition: This clinical trial is an non-interventional observational clinical study, measuring the plasma levels of the levobupivicaine during labour with an epidural infusion. We will measure levels in pre-... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002455-97 | Sponsor Protocol Number: 13381 | Start Date*: 2016-10-19 | ||||||||||||||||
Sponsor Name:University of Southampton | ||||||||||||||||||
Full Title: Antibiotics for lower Respiratory Tract Infection in Children presenting in Primary Care | ||||||||||||||||||
Medical condition: Respiratory tract infections in children aged between 6 months and 12 years | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-003410-12 | Sponsor Protocol Number: RG_19-169 | Start Date*: 2020-12-16 |
Sponsor Name:University of Birmingham | ||
Full Title: Pregnancy ANtihypertensive Drugs: which Agent is best? | ||
Medical condition: Hypertension in pregnancy (chronic hypertension, gestational hypertension or pre-eclampsia) | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
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