- Trials with a EudraCT protocol (44,400)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18,700)
44,400 result(s) found.
Displaying page 2,075 of 2,220.
| EudraCT Number: 2022-001989-36 | Sponsor Protocol Number: SIGN | Start Date*: 2022-09-07 |
| Sponsor Name:Med. Univ. Wien, Klinik f. Innere Med I, Onkologie | ||
| Full Title: Selective serotonin reuptake inhibition in patients with advanced gastroesophageal cancer receiving immunochemotherapy: a prospective phase II trial | ||
| Medical condition: gastroesophageal cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2006-006971-19 | Sponsor Protocol Number: | Start Date*: Information not available in EudraCT | |||||||||||||||||||||
| Sponsor Name:Aker universitetssykehus | |||||||||||||||||||||||
| Full Title: Effect of Aggrenox® / Asasantin® Retard compared with Clopidogrel on Endothelial function as measured by Microalbuminuria, Inflammatory markers CRP, MCP-1, and MMP-9 in Patients with Type 2 Diabet... | |||||||||||||||||||||||
| Medical condition: Patients with Type 2 Diabetes Mellitus and a history of TIA or stroke. | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: NO (Completed) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2008-006253-41 | Sponsor Protocol Number: DC-004 | Start Date*: 2012-01-05 |
| Sponsor Name:The Norwegian Radium Hospital, Oslo University Hospital | ||
| Full Title: Phase I/II trial for vaccine therapy with hTERT-, survivin- and tumor cell derived mRNA + ex vivo T cell expansion and reinfusion in patients with metastatic malignant melanoma | ||
| Medical condition: Malignant melanoma stage IV M1c or better | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-001956-40 | Sponsor Protocol Number: PK_pregnancy | Start Date*: 2023-03-05 |
| Sponsor Name:Medical University Vienna | ||
| Full Title: Antibiotic pharmacokinetics in women with twin pregnancy | ||
| Medical condition: The target population are twin pregnancy women that will deliver through c-section and that are receiving one or more of the included antibiotics. | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: AT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-006802-40 | Sponsor Protocol Number: 1 | Start Date*: 2010-12-16 |
| Sponsor Name:Karolinska University Hospital | ||
| Full Title: A PHASE II STUDY WITH OXALIPLATIN + 5FU + CETUXIMAB AND RADIOTHERAPY FOR TREATMENT OF NON-RESECTABLE, LOCALLY ADVANCED BUT NOT METASTATIC CANCER OF OESOPHAGUS OR THE CARDIA REGION | ||
| Medical condition: Patients with histologically verified inoperable, locally advanced but non metastastic oesophageal ca or the ca of cardia region | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Prematurely Ended) DK (Completed) NO (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-003532-73 | Sponsor Protocol Number: ADVANCE-AD04-001 | Start Date*: 2023-05-02 | ||||||||||||||||
| Sponsor Name:ADvantage Therapeutics GmbH | ||||||||||||||||||
| Full Title: A Phase 2b, Multicenter, Randomized, Placebo-controlled, Double-blind Study to Assess the Safety and Efficacy of AD04 in Patients with Early Alzheimer’s Disease - ADVANCE | ||||||||||||||||||
| Medical condition: early Alzheimer’s disease | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SK (Prematurely Ended) DE (Completed) FR (Completed) AT (Trial now transitioned) BG (Completed) PL (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2008-006742-26 | Sponsor Protocol Number: NIS-GEU-DUM-2008/1 | Start Date*: 2009-01-08 |
| Sponsor Name:AstraZeneca AS | ||
| Full Title: Symptomatic versus Endoscopic approach for the Diagnosis and Initial treatment of Gastroesophageal Reflux Disease using GerdQ | ||
| Medical condition: Diagnosis and initial treatment of gastroesofageal reflux disease. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Completed) IT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-011112-37 | Sponsor Protocol Number: 2009-3 | Start Date*: 2009-08-04 |
| Sponsor Name:Dept. of Anaesthesia, Oslo University Hospital, Ullevål | ||
| Full Title: Dexmedetomidine versus midazolam til sedasjon av pediatriske intensivpasienter ved Oslo Universitetssykehus. | ||
| Medical condition: Paediatric patients requiring mecanical ventilation and sedation in PICU. | ||
| Disease: | ||
| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: NO (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-000733-14 | Sponsor Protocol Number: DAPA-HD | Start Date*: 2022-07-18 |
| Sponsor Name:Medical University of Vienna | ||
| Full Title: SGLT2 INHIBITION (DAPAGLIFLOZIN) IN DIABETIC AND NON-DIABETIC HEMODIALYSIS PATIENTS WITH AND WITHOUT RESIDUAL URINE VOLUME: A PROSPECTIVE RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLINDED PHASE II TRIAL | ||
| Medical condition: Cardiovascular Outcome | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-016924-30 | Sponsor Protocol Number: NorCAPITAL | Start Date*: Information not available in EudraCT |
| Sponsor Name:Division of Paediatrics, Rikshospitalet University Hospital | ||
| Full Title: NorCAPITAL The Norwegian Study of Chronic Fatigue Syndrome in Adolescents: Pathophysiology and Intervention Trial | ||
| Medical condition: Chronic fatigue syndrom/myalgic encephalomyelitis (CFS/ME) in adolescents | ||
| Disease: | ||
| Population Age: Adolescents, Under 18 | Gender: Male, Female | |
| Trial protocol: NO (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-019577-16 | Sponsor Protocol Number: EGF114299 | Start Date*: 2010-12-21 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A Phase III trial to compare the safety and efficacy of lapatinib plus trastuzumab plus an aromatase inhibitor (AI) versus trastuzumab plus an AI versus lapatinib plus an AI as first- or second-lin... | |||||||||||||
| Medical condition: HER2-positive metastatic breast cancer who have received prior trastuzumab and endocrine therapies | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) HU (Completed) IE (Prematurely Ended) PL (Completed) BE (Completed) BG (Prematurely Ended) NO (Prematurely Ended) GB (Completed) LT (Prematurely Ended) PT (Prematurely Ended) ES (Ongoing) GR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-020415-36 | Sponsor Protocol Number: SUS2010GOLA01 | Start Date*: 2010-07-15 |
| Sponsor Name:Stavanger University Hospital | ||
| Full Title: En åpen, randomisert cross over studie av fosfatbinder (sevelamer) eller aktivt vitamin D hos pasienter med kronisk nyresvikt i stadium 3b (eGFR 30-45 ml/min/1,73 m2) for evaluering av fibroblast l... | ||
| Medical condition: Chronic renal failure, stage 3B. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NO (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-020233-56 | Sponsor Protocol Number: DC-006 | Start Date*: 2011-03-24 |
| Sponsor Name:Oslo University Hospital | ||
| Full Title: PHASE I/II TRIAL OF VACCINE THERAPY IN RELAPSED AND PLATINUM RESISTANT EPITHELIAL OVARIAN CANCER PATIENTS USING AUTOLOGOUS DENDRITIC CELLS LOADED WITH AMPLIFIED OVARIAN CANCER STEM CELL mRNA, hTE... | ||
| Medical condition: Relapsed and platinum resistant epithelial ovarian carcinoma patients that have received one line of non-platinum chemotherapy in resistance disease setting. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: NO (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2010-023125-38 | Sponsor Protocol Number: NLG-LBC05 | Start Date*: 2011-01-21 | |||||||||||||||||||||
| Sponsor Name:Nordic Lymphoma Group | |||||||||||||||||||||||
| Full Title: Dose densified chemoimmunotherapy with early CNS prophylaxis in patients less than 65 years with high risk (aaIPI≥2) Diffuse Large B-Cell Lymphoma. | |||||||||||||||||||||||
| Medical condition: Diffuse large B-cell lymphoma (DLBCL) | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: SE (Temporarily Halted) FI (Completed) NO (Completed) DK (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2010-022949-17 | Sponsor Protocol Number: ET-D-009-10 | Start Date*: 2010-10-20 | |||||||||||
| Sponsor Name:IST. DI RICERCHE FARMACOLOG. M. NEGRI | |||||||||||||
| Full Title: Phase III international, randomized study of Trabectedin plus Pegylated Liposomal Doxorubicin (PLD) versus Carboplatin plus PLD in patients with ovarian cancer progressing within 6-12 months of las... | |||||||||||||
| Medical condition: Advanced ovarian cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: IT (Completed) GB (GB - no longer in EU/EEA) FI (Completed) BE (Completed) NL (Ongoing) DK (Completed) DE (Completed) ES (Completed) AT (Completed) NO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-023129-39 | Sponsor Protocol Number: MP4OX-10-TRA-205 | Start Date*: 2011-03-22 | ||||||||||||||||
| Sponsor Name:Sangart, Inc. | ||||||||||||||||||
| Full Title: Estudio multicéntrico, aleatorizado, en doble ciego y controlado, para evaluar la seguridad y la eficacia del tratamiento con MP4OX, añadido al tratamiento habitual, en pacientes con traumatismo se... | ||||||||||||||||||
| Medical condition: Pacientes con traumatismo severo y acidosis láctica por shock hemorrágico.//Severely injured trauma patients with lactic acidosis due to hemorrhagic shock. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: ES (Ongoing) AT (Completed) DE (Completed) GB (Completed) NO (Completed) IT (Ongoing) BE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2010-023740-32 | Sponsor Protocol Number: 2010-023740-32 | Start Date*: 2011-05-18 | |||||||||||
| Sponsor Name:Haukeland University Hospital [...] | |||||||||||||
| Full Title: Pharmacogenomics of Mood Stabilizer Response in Bipolar Disorder | |||||||||||||
| Medical condition: The goal of this work is to identify genes associated with good response of bipolar patients to two commonly used mood stabilizing agents, lithium and valproate. 1. All patients will be started on ... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NO (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-001639-21 | Sponsor Protocol Number: NMDSG10B | Start Date*: 2011-11-01 | |||||||||||
| Sponsor Name:NMDSG Nordics Myeloplastics Syndrom Study Group | |||||||||||||
| Full Title: A multicentre open randomized phase II study of the efficacy and safety of azacitidine alone or in combination with lenalidomide in high-risk myeloid disease (high-risk MDS and AML) with a karyotyp... | |||||||||||||
| Medical condition: Myelodysplastic syndrome and acute myeloid leukemia with a deletion of 5q | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) FI (Completed) NO (Completed) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001068-23 | Sponsor Protocol Number: ACO CT 2010-01 | Start Date*: 2011-07-26 | |||||||||||
| Sponsor Name:ACO Hud Nordic AB | |||||||||||||
| Full Title: Comparison of Moisturisers for the Prevention of Atopic Dermatitis Relapse– a Randomised, Double Blind Controlled Study (COMPADRE) | |||||||||||||
| Medical condition: Atopic dermatitis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FI (Completed) NO (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-003576-36 | Sponsor Protocol Number: ARD11586(MM-121-04-02-08) | Start Date*: 2012-04-20 | |||||||||||
| Sponsor Name:MERRIMACK PHARMACEUTICALS | |||||||||||||
| Full Title: A Phase II Randomized Open Label Study of MM-121 in combination with Paclitaxel versus Paclitaxel alone in patient with Platinum Resistant/Refractory Advanced Ovarian Cancers. | |||||||||||||
| Medical condition: Patient with Platinum Resistant/Refractory Advanced Ovarian Cancers. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: BE (Completed) CZ (Completed) FR (Ongoing) ES (Ongoing) IT (Completed) NO (Completed) DE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
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