- Trials with a EudraCT protocol (73)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
73 result(s) found for: Patient transport.
Displaying page 1 of 4.
EudraCT Number: 2011-005366-38 | Sponsor Protocol Number: 2011-112 | Start Date*: 2012-02-26 |
Sponsor Name:Ambulance Service, Stockholm City Council | ||
Full Title: Treatment of pain in Ambulance Services with Sufenta® nasally compared to Morfin® intravenously. | ||
Medical condition: Severe pain treated in ambulance service. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001103-17 | Sponsor Protocol Number: INSTI01 | Start Date*: 2021-01-11 |
Sponsor Name:Cliniques universitaires Saint-Luc | ||
Full Title: Gut microbiota, pharmacogenetics and Integrase Strand Transfer Inhibitors response | ||
Medical condition: HIV infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-000592-24 | Sponsor Protocol Number: PTH2008002 | Start Date*: 2008-08-11 | |||||||||||
Sponsor Name:Berufsgenossenschaftliche Unfallklinik | |||||||||||||
Full Title: A Randomized Open Clinical Study of Daily Subcutaneous Parathyroid Hormone (1-34) / Teriparatide Injection on the Consolidation of Regenerated Bone Formed after Distraction Osteogenesis. | |||||||||||||
Medical condition: Patients with tibial bone defects due to resection after osteomyelitis who are undergoing bone segment transport | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005536-17 | Sponsor Protocol Number: UX007G-CL301 | Start Date*: 2017-05-17 | |||||||||||
Sponsor Name:Ultragenyx Pharmaceutical Inc | |||||||||||||
Full Title: A Phase 3, randomized, double-blind, placebo-controlled, crossover study to assess the efficacy and safety of UX007 in the treatment of movement disorders associated with Glucose Transporter Type 1... | |||||||||||||
Medical condition: Glucose Transporter Type 1 deficiency syndrome | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) ES (Prematurely Ended) FR (Completed) GB (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017253-35 | Sponsor Protocol Number: PS1/001/09 | Start Date*: 2010-08-20 |
Sponsor Name:Oxford BioMedica (UK) Ltd | ||
Full Title: A multicentre, open-label extension study to determine the long term safety, tolerability and efficacy of ProSavin® in patients with bilateral, idiopathic Parkinson’s disease | ||
Medical condition: Patients with bilateral, idiopathic Parkinson's Disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005286-69 | Sponsor Protocol Number: 7502 | Start Date*: 2015-02-23 |
Sponsor Name:Kuopion yliopistollinen sairaala/Ensihoitokeskus | ||
Full Title: Intranasal fentanyl in pre-hospital analgesia | ||
Medical condition: Patients with trauma, musculoskeletal, stomach or back pain on numeric rating scale at least value 4 | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2010-019380-11 | Sponsor Protocol Number: 09/0278 | Start Date*: 2010-09-30 |
Sponsor Name: | ||
Full Title: Autologous cell therapy of fracture non-union – cell phenotype as a predictor of outcome | ||
Medical condition: delayed fracture union (fracture non-union) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005664-10 | Sponsor Protocol Number: BMP2/1 | Start Date*: 2015-09-30 |
Sponsor Name:UZ Leuven Orthopedic research | ||
Full Title: InductOs® (rhBMP-2; dibotermin alfa) vs. autologous bone grafting for the treatment of nonunion of the docking site in tibial bone transport | ||
Medical condition: fractured non-healing tibia | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-001988-36 | Sponsor Protocol Number: CCD-LMZYMAA1-08 | Start Date*: 2016-10-05 | |||||||||||
Sponsor Name:Chiesi Farmaceutici S.p.A. | |||||||||||||
Full Title: A 24-month Multicenter, Open-label Phase II Trial Investigating the Safety and Efficacy of Repeated velmanase alfa (recombinant human alpha-mannosidase) Treatment in Pediatric Patients below 6 year... | |||||||||||||
Medical condition: Alfa-mannosidosis | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) DE (Completed) AT (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001450-66 | Sponsor Protocol Number: 2007-001450-66 | Start Date*: 2007-09-26 |
Sponsor Name:Karolinska Institutet | ||
Full Title: Improved management of depression in primary health care – a randomized study of two structured programs with reference to the role of genetic predisposition | ||
Medical condition: To evaluate different treatment alternatives, including psychological intervention, in depressed patients recruited by screening in participating GP:s waiting-rooms (opportunistic screening). In o... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001459-35 | Sponsor Protocol Number: MC/PR/1400/007/11 | Start Date*: 2012-12-20 | |||||||||||
Sponsor Name:CHIESI | |||||||||||||
Full Title: MULTICENTRE, RANDOMISED, DOUBLE-BLIND, PARALLEL GROUP, PLACEBO-CONTROLLED STUDY ON THE THERAPEUTIC EFFICACY AND SAFETY OF BECLOMETHASONE DIPROPIONATE SUSPENSION FOR INHALATION 800 micrograms TWICE... | |||||||||||||
Medical condition: Acute rhinosinusitis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005843-24 | Sponsor Protocol Number: RIFA+UDCA | Start Date*: 2006-02-23 |
Sponsor Name:Hanns-Ulrich Marschall | ||
Full Title: Studie på effekten av rifampicin och ursodeoxycholsyra på gallipider och deras transport och avgiftning hos patienter med kolesterolgallstenar. | ||
Medical condition: Gallstone disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004126-56 | Sponsor Protocol Number: NUTH-2005-03523 | Start Date*: 2006-03-07 |
Sponsor Name:Newcastle upon Tyne Hospitals NHS Trust | ||
Full Title: Observational pharmacokinetic study of doxorubicin and cyclophosphamide in patients with early breast cancer. | ||
Medical condition: Early breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001972-19 | Sponsor Protocol Number: Feno Atorva | Start Date*: 2007-01-22 | |||||||||||
Sponsor Name:Hanns-Ulrich Marschall | |||||||||||||
Full Title: Study of atorvastatin and fenofibrate mediated effects on the metabolism and hepatic excretion of biliary compounds in gallstone patients. | |||||||||||||
Medical condition: Gallstone disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002187-26 | Sponsor Protocol Number: neostigmine2019 | Start Date*: 2019-08-28 |
Sponsor Name:KU Leuven - TARGID | ||
Full Title: A Prospective evaluation of the effect of a single dose of neostigmine in patients with patients with weak or absent esophageal peristalsis | ||
Medical condition: Patients with complaints of dysphagia and poor esophageal motility | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-003950-15 | Sponsor Protocol Number: rhLAMAN-10 | Start Date*: 2015-01-22 | |||||||||||
Sponsor Name:Zymenex A/S | |||||||||||||
Full Title: A single center, open label clinical trial investigating the long-term efficacy of rhLAMAN (recombinant human alpha-mannosidase or Lamazym) treatment in subjects with alpha-Mannosidosis who previo... | |||||||||||||
Medical condition: alpha-Mannosidosis | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-002239-29 | Sponsor Protocol Number: WI18274 | Start Date*: 2006-03-06 |
Sponsor Name:F. Hoffmann - La Roche AG | ||
Full Title: A phase II prospective, open label, randomized, active-controlled, parallel group, multi-center ‘proof of concept’ trial in adult patients with complicated skin and skin structure infections requir... | ||
Medical condition: Treatment of adult patients with complicated skin and skin structure infections requiring hospitalization. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: LT (Completed) EE (Completed) DE (Completed) LV (Completed) HU (Completed) GR (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-001452-11 | Sponsor Protocol Number: 201103 | Start Date*: 2011-06-07 |
Sponsor Name:Skånes Universitetssjukhus Lund | ||
Full Title: Supplemental Oxygen in Catherized Coronary Emergency Reperfusion | ||
Medical condition: Acute ST elevation myocardial infaction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000048-73 | Sponsor Protocol Number: AMT-101-201 | Start Date*: 2020-09-24 | |||||||||||
Sponsor Name:Applied Molecular Transport Inc. | |||||||||||||
Full Title: A Combined Phase 2/3 12-week, Randomized, Double-blind, Placebo-controlled Study Investigating the Efficacy of AMT-101 in Subjects with Chronic Antibiotic-resistant Pouchitis | |||||||||||||
Medical condition: Pouchitis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) HU (Completed) DE (Completed) NL (Completed) BE (Completed) IT (Completed) IE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000447-27 | Sponsor Protocol Number: USKH_VL1 | Start Date*: 2012-07-25 |
Sponsor Name:Universitätsklinikum Schleswig-Holstein, Campus Kiel | ||
Full Title: Open Label Study for the Functional Characterization of Drug Metabolism and Transport in patients before routine visceral surgery | ||
Medical condition: Pharmacokinetic trial in patients, with a good general condition before standard abdominal surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Temporarily Halted) | ||
Trial results: (No results available) |
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