- Trials with a EudraCT protocol (26,267)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (9,945)
26,267 result(s) found for: NA.
Displaying page 48 of 1,314.
| EudraCT Number: 2005-003148-79 | Sponsor Protocol Number: 08/05 | Start Date*: 2006-03-21 |
| Sponsor Name:Wirral Hospitals NHS Trust | ||
| Full Title: Role of antibiotic line locks in the prevention of tunnelled haemodialysis catheter infection: a double blind randomised controlled trial. | ||
| Medical condition: Tunnelled haemodialysis catheter related infection. These infections are common (approximately 2-7 infections per 1000 catheter days) in patients on haemodialysis; we aim to assess the efficacy of ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-002520-41 | Sponsor Protocol Number: Projektid: GA vs spinal-morfin anes | Start Date*: 2007-01-29 |
| Sponsor Name:Kvinnokliniken | ||
| Full Title: Generell anestesi versus Spinal-morfin anestesi vid hysterektomi En randomiserad prospektiv öppen studie | ||
| Medical condition: Benigna gynekologiska tillstånd som ger indikation för abdominell hysterektomi | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-000108-15 | Sponsor Protocol Number: KCL/SLAM-CT2005-01 | Start Date*: 2005-03-11 |
| Sponsor Name:Institute of Psychiatry, Kings College London & South London and Maudsley NHS Trust | ||
| Full Title: Pharmacokinetic and pharmacodynamic properties of oral, intramuscular and intravenous methadone in methadone maintenance patients | ||
| Medical condition: Opioid dependence | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Temporarily Halted) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-002237-20 | Sponsor Protocol Number: ATS K021 | Start Date*: 2006-08-21 |
| Sponsor Name:Takeda Pharma GmbH | ||
| Full Title: Pilot trial studying the Effects of Pioglitazone in Comparison to Placebo on Myocardial Function and Oxidative Stress in Patients with Type II Diabetes and Insulin Resistance undergoing elective PTCA | ||
| Medical condition: Type 2 diabetic patients treated with oral agents except PPAR gamma agonists and / or patients with insulin resistance measured by IRIS score > 50 with stable coronary artery disease and supposed e... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-005022-31 | Sponsor Protocol Number: AI424-172 | Start Date*: 2006-01-31 |
| Sponsor Name:Bristol-Myers Squibb International Corporation | ||
| Full Title: Effect of a High-Fat or a Light Meal Relative to Fasting Conditions on the Pharmacokinetics of Atazanavir when Administered with Ritonavir in Healthy Subjects | ||
| Medical condition: Healthy subjects | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-002192-32 | Sponsor Protocol Number: UKSH-A105 | Start Date*: 2006-07-28 |
| Sponsor Name:Univeristy Hospital Schleswig-Holstein | ||
| Full Title: Phase II Randomized, Parallel-Group Trial on PTK-ZK with or without DTIC in Patients with non-resectable Metastatic Malignant Melanoma | ||
| Medical condition: non-resectable metastatic malignant melanoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-006076-38 | Sponsor Protocol Number: RLBUHT3173 | Start Date*: 2007-04-26 |
| Sponsor Name:University of Liverpool [...] | ||
| Full Title: The Liverpool HIV TDM Registry: Studying influences upon plasma HIV drug exposure | ||
| Medical condition: Pharmacogenetic study of HIV+ patients receiving antiretroviral therapy. We wish to correlate drug concentration with host genetic patients receiving certain HIV drugs. No dosage modification wil... | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-002623-41 | Sponsor Protocol Number: endo 220604 | Start Date*: 2004-09-10 |
| Sponsor Name:Anders Nyboe Andersen, klinikchef, dr. med., Fertilitetsklinikken afsnit 4071, Rigshospitalet | ||
| Full Title: Anvendelse af aromatase-inhibitor (Arimidex) i kombination med GnRH agonist (Zoladex) som forbehandling til IVF hos patienter med ovariel endometriose | ||
| Medical condition: endometriosis ovarii | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-001133-15 | Sponsor Protocol Number: 19.4.208B | Start Date*: 2005-09-08 |
| Sponsor Name:NV Organon | ||
| Full Title: A multi-center, randomized, open-label, prospective bridging, parallel dosefinding trial comparing efficacy, safety and pharmacokinetics of 4 doses of Org 25969 and placebo administered at reappear... | ||
| Medical condition: Not applicable | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: SE (Completed) BE (Completed) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2007-001906-26 | Sponsor Protocol Number: 2007-22-INJ-17 | Start Date*: 2008-09-10 | |||||||||||
| Sponsor Name:HEXAL AG | |||||||||||||
| Full Title: Randomized, controlled, double-blind multicenter safety study to evaluate the safety and immunogenicity of subcutaneous EPO HEXAL vs. ERYPO® in the treatment of anemia associated with chronic renal... | |||||||||||||
| Medical condition: anemia associated with chronic renal insufficiency in predialysis patients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) SK (Completed) FR (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-000540-24 | Sponsor Protocol Number: CLAF237A2310 | Start Date*: 2004-12-15 |
| Sponsor Name:Novartis Pharma Services AG | ||
| Full Title: A multicenter, double-blind, randomized, active controlled study to compare the effect of long term treatment with LAF237 50 mg bid to gliclazide up to 320 mg daily in drug naïve patients with type... | ||
| Medical condition: Type II Diabetes | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) IE (Completed) GB (Completed) DE (Completed) IT (Completed) ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-000117-34 | Sponsor Protocol Number: Nordic VII | Start Date*: 2005-04-22 |
| Sponsor Name:The Nordic Colorectal Cancer Biomodulation Group | ||
| Full Title: Combination of 5-Fluorouracil/Folinate/Oxaliplatin (Eloxatin®) (FLOX regimen) with Concomitant or Concomitant and Maintenance Administration of Cetuximab (Erbitux®), in First-Line Treatment of Meta... | ||
| Medical condition: Patient with metastatic colorectal cancer. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) IS (Completed) FI (Completed) DK (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-000395-41 | Sponsor Protocol Number: ICORG 05-01 | Start Date*: 2005-05-27 |
| Sponsor Name:All Ireland co-operative Oncology Research Group | ||
| Full Title: Phase II Study to Assess the Safety, Efficacy, and Tolerability of Combination Therapy with Velcade (Bortezomib), Adriamycin, and Dexamethasone (PAD) as Therapy for Patients with relapsed or refra... | ||
| Medical condition: Relapsed or refractory Multiple Myeloma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (GB - no longer in EU/EEA) IE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2004-002629-36 | Sponsor Protocol Number: 0881A6-101764 | Start Date*: 2005-02-01 |
| Sponsor Name:Wyeth Pharmaceuticals, Global Medical Affairs Department | ||
| Full Title: A Randomized, Open Label Study to Evaluate the Safety and Efficacy of Etanercept in the Treatment of Subjects with Psoriasis | ||
| Medical condition: psoriasis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: HU (Completed) AT (Completed) SE (Completed) IE (Completed) DK (Completed) FI (Completed) CZ (Completed) DE (Completed) GB (Completed) IT (Completed) BE (Completed) ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-000538-19 | Sponsor Protocol Number: CLIN004-0009 | Start Date*: 2005-04-21 | |||||||||||
| Sponsor Name:DURECT Corporation | |||||||||||||
| Full Title: Protocol CLIN004−0009 (February 02, 2005): A Pharmacodynamic/Pharmacokinetic Study of SABER−Bupivacaine and/or Bupivacaine HCl Administered Intra−operatively During Open Inguinal Hernia Repair unde... | |||||||||||||
| Medical condition: Inguinal hernia repair | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-000677-21 | Sponsor Protocol Number: CMC-P004 | Start Date*: 2005-05-20 |
| Sponsor Name:CMC Contrast AB | ||
| Full Title: Evaluation of the diagnostic quality of CMC-001 (manganese chloride tetrahydrate) in liver MR-imaging in patients with liver metastases in comparison to Gadolinium BOPTA. A randomised cross-over Ph... | ||
| Medical condition: Liver metastases. CMC-001 is an orally administered contrast medium containing manganese (Mn) as the active imaging substance. Manganese is absorbed by the healthy parts of the liver and will thus ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-004396-35 | Sponsor Protocol Number: 06078SE-A | Start Date*: 2006-10-25 |
| Sponsor Name:Belfast City Hospital Trust | ||
| Full Title: Investigation of the anti-inflammatory effects of simvastatin in a model of acute lung injury after inhalation of lipopolysaccharide by healthy volunteers | ||
| Medical condition: Acute lung injury (ALI) | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2006-000368-10 | Sponsor Protocol Number: NEX-426-MEI-0040-I | Start Date*: 2006-08-10 |
| Sponsor Name:Tecnical University of Munich | ||
| Full Title: High-dose therapy with Esomeprazol in combination with Baclofen therapy for symptomatic therapy-resistant gastrooesophageal reflux disease. | ||
| Medical condition: Gastroesophageal reflux disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2005-001297-27 | Sponsor Protocol Number: BRN03 | Start Date*: 2005-06-08 |
| Sponsor Name:Neolab td | ||
| Full Title: Comparative Efficacy & Safety of Two Intranasal Fluticasone Propionate Formulations in Persistent Allergic Rhinitis | ||
| Medical condition: Persistent allergic rhinitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-001299-19 | Sponsor Protocol Number: GJNH-06-01 | Start Date*: 2006-05-12 |
| Sponsor Name:Golden Jubilee National Hospital | ||
| Full Title: Prospective randomised trial comparing intraoperative topical Quixil and intravenous tranexamic acid in reduction of blood loss following primary hip and knee joint replacement surgery | ||
| Medical condition: Elective total knee replacement and total hip replacement. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
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