- Trials with a EudraCT protocol (9,517)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
9,517 result(s) found for: e.
Displaying page 195 of 476.
| EudraCT Number: 2020-004202-60 | Sponsor Protocol Number: CER-001-SEP_AKI_01 | Start Date*: 2021-01-13 | |||||||||||
| Sponsor Name:CERENIS THERAPEUTICS | |||||||||||||
| Full Title: A RAndomized pilot study comparing short-term CER-001 infusions at different doses to prevent Sepsis-induced acute kidney injury | |||||||||||||
| Medical condition: Sepsis due to intra-abdominal cavity infection or urosepsis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004704-34 | Sponsor Protocol Number: RECIR | Start Date*: 2021-03-16 | |||||||||||
| Sponsor Name:FONDAZIONE POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI IRCCS UNIVERSITA' CATTOLICA DEL SACRO CUORE | |||||||||||||
| Full Title: Recovery from deep neuromuscular blockade using different sugammadex doses in elderly patients undergoing laparoscopic robot-assisted prostatectomy: a prospective, randomized, double-blind clinical... | |||||||||||||
| Medical condition: Deep neuromuscular block in patients undergoing RALP under general anaesthesia | |||||||||||||
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| Population Age: Elderly | Gender: Male | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2015-001434-16 | Sponsor Protocol Number: 3D_CHB/collacone | Start Date*: 2016-03-30 | |||||||||||
| Sponsor Name:Universitätsmedizin Greifswald, KöR | |||||||||||||
| Full Title: A method for measuring volume changes of the alveolar ridge during dental implantation using 3D scanning | |||||||||||||
| Medical condition: alveolar ridge atrophy | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-002101-25 | Sponsor Protocol Number: FDA02_AIM3 | Start Date*: 2020-09-14 |
| Sponsor Name:HEALTH – Institute for Biomedicine and Health Sciences, JOANNEUM RESEARCH Forschungsgesellschaft mbH | ||
| Full Title: A SINGLE CENTER, OPEN-LABEL, CLINICAL STUDY TO EVALUATE THE ABILITY OF DERMAL OPEN FLOW MICROPERFUSION (DOFM) FOR BIOEQUIVALENCE TESTING OF TOPICALLY APPLIED DICLOFENAC SODIUM PRODUCTS IN HEALTHY S... | ||
| Medical condition: Healthy Volunteers | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-001601-82 | Sponsor Protocol Number: MR311-3506(AMBU-001) | Start Date*: 2019-07-08 |
| Sponsor Name:Mundipharma Pharmaceuticals B.V. | ||
| Full Title: Open randomized clinical trial to compare pain relief between low-dose methoxyflurane and standard of care for the treatment of patients with trauma pain in emergency medical services in the Nether... | ||
| Medical condition: Patients with moderate trauma pain due to extremity injuries for whom the emergency medical services have been called. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-000463-40 | Sponsor Protocol Number: OCTO_049 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:University of Oxford | |||||||||||||
| Full Title: A Sequential Phase I study of MEK1/2 inhibitors PD-0325901 or Binimetinib combined with cMET inhibitor Crizotinib in RAS Mutant and RAS Wild Type(with aberrant c-MET) Colorectal Cancer | |||||||||||||
| Medical condition: Cancer. Solid tumours in the escalation phase and colorectal cancer in the expansion groups. | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) IE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-019815-40 | Sponsor Protocol Number: ML25359 | Start Date*: 2011-03-24 | |||||||||||
| Sponsor Name:Skåne University Hospital, Department of Oncology | |||||||||||||
| Full Title: Avastin and chemotherapy followed by a KRAS stratified randomization to maintenance treatment for first line treatment of metastatic colorectal cancer | |||||||||||||
| Medical condition: Patients with previously untreated metastatic colorectal carcinoma. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002835-32 | Sponsor Protocol Number: BP29392 | Start Date*: 2015-01-26 | |||||||||||
| Sponsor Name:Roche Farma, S.A. en nombre de F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: AN OPEN-LABEL, MULTICENTER, DOSE-ESCALATION PHASE IB STUDY TO INVESTIGATE THE SAFETY, PHARMACOKINETICS, PHARMACODYNAMICS, AND THERAPEUTIC ACTIVITY OF RO7009789 (CD40 AGONIST) IN COMBINATION WITH MP... | |||||||||||||
| Medical condition: Locally Advanced and/ or Metastatic Solid Tumors | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000838-64 | Sponsor Protocol Number: D6470C00003 | Start Date*: 2017-11-10 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A Phase 2a, Randomised, Double-blind, Parallel Study to Assess the Efficacy, Safety and Tolerability of AZD9567 compared to Prednisolone 20 mg in patients with active Rheumatoid Arthritis (RA) | |||||||||||||
| Medical condition: Rheumatoid Arthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Prematurely Ended) DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-001635-27 | Sponsor Protocol Number: AB20001 | Start Date*: 2020-05-04 | |||||||||||
| Sponsor Name:AB Science | |||||||||||||
| Full Title: A Randomized, Double-blind, Placebo-controlled Phase 2 Clinical Trial to Evaluate the Safety and Efficacy of Masitinib combined with Isoquercetin, and Best Supportive Care in Hospitalized Patients ... | |||||||||||||
| Medical condition: Hospitalized Moderate and Severe COVID-19 Patients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) ES (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2018-003693-27 | Sponsor Protocol Number: CHDR1854 | Start Date*: 2019-02-06 |
| Sponsor Name:Leiden University Medical Center | ||
| Full Title: Intraoperative near-infrared fluorescence imaging of endometriosis with OTL38: a pilot study | ||
| Medical condition: Endometriosis | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-001538-25 | Sponsor Protocol Number: AIO-HEP-0117 | Start Date*: 2018-03-12 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:AIO-Studien-gGmbH | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: A randomized phase II trial of durvalumab and tremelimumab with gemcitabine or gemcitabine and cisplatin compared to gemcitabine and cisplatin in treatment-naïve patients with cholangio- and gallbl... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: advanced, unresectable and/or metastatic cholangio- and gallbladder carcinoma | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2016-004527-23 | Sponsor Protocol Number: MM1636 | Start Date*: 2017-03-14 | |||||||||||
| Sponsor Name:Center for Cancer Immune Therapy | |||||||||||||
| Full Title: Combination therapy with Nivolumab and PD-L1/IDO peptide vaccine with Montanide to patients with metastatic malignant melanoma | |||||||||||||
| Medical condition: Metastatic malignant melanoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004978-22 | Sponsor Protocol Number: OPHT-300920 | Start Date*: 2021-01-21 |
| Sponsor Name:Medical University of Vienna, Department of Clinical Pharmacology | ||
| Full Title: Detection of acetylsalicylic acid and omega-3 fatty acids in Schirmers’ test strips using mass spectrometry and correlations with tear film and blood flow parameters in healthy adults: an open-labe... | ||
| Medical condition: Healthy subjects | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-005422-30 | Sponsor Protocol Number: AIO-KRK-0212 | Start Date*: 2014-01-09 | |||||||||||
| Sponsor Name:AIO Studien gGmbH | |||||||||||||
| Full Title: Randomized Phase II study for evaluation of efficacy and safety of maintenance treatment with 5-FU/FA plus panitumumab vs. 5-FU/FA alone after prior induction treatment with mFOLFOX6 plus panitumum... | |||||||||||||
| Medical condition: Metastatic colorectal cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-005010-19 | Sponsor Protocol Number: HCB/2019/1148 | Start Date*: 2020-08-21 |
| Sponsor Name:Hospital Clínic de Barcelona | ||
| Full Title: Ultrasound-guided Genicular Nerve Block an Analgesic Alternative to LIA for Total Knee Arthroplasty. Randomized clinical trial. | ||
| Medical condition: Total knee arthroplasty has become one of the most frequent surgical procedures in the world. Currently models employ high volume local infiltration analgesia (LIA) techniques. The genicular nerve ... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-000925-27 | Sponsor Protocol Number: ProF-001_Phase_IIb/III | Start Date*: 2019-08-27 | |||||||||||
| Sponsor Name:Profem GmbH | |||||||||||||
| Full Title: A phase IIb/III, parallel-arm, randomized, active-controlled, double-blind, double-dummy, study in patients with recurrent vulvovaginal candidiasis to compare the clinical efficacy, safety and tole... | |||||||||||||
| Medical condition: recurrent vulvovaginal candidiasis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: AT (Completed) SK (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2023-000764-58 | Sponsor Protocol Number: 219967 | Start Date*: 2023-10-03 |
| Sponsor Name:GlaxoSmithKline Biologicals SA | ||
| Full Title: A Phase 4, single-arm, open-label, multi-center study to assess the immune response and safety of the meningococcal Group B vaccine MenB+OMV NZ when administered to healthy infants from 2 months of... | ||
| Medical condition: Healthy volunteers (active immunization of infants against invasive meningococcal disease (IMD) due to N. meningitidis serogroup B infection). | ||
| Disease: | ||
| Population Age: Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2016-001452-22 | Sponsor Protocol Number: SJ-641 | Start Date*: 2018-08-29 | ||||||||||||||||
| Sponsor Name:Zealand University Hospital | ||||||||||||||||||
| Full Title: Treatment effect of colesevelam for bile acid diarrhoea | ||||||||||||||||||
| Medical condition: Bile acid diarrhoea | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2010-024328-53 | Sponsor Protocol Number: HULPOFT-2010-01 | Start Date*: 2012-05-14 |
| Sponsor Name:Fundación para la Investigación Biomédica del Hospital Universitario La Paz | ||
| Full Title: Phase IIa clinical trial to determine the feasibility and safety of using autologous expanded stem cell (ASC) from fat in the treatment of keratopathy associated with bilateral limbic insufficiency | ||
| Medical condition: Keratopathy associated with bilateral limbic insufficiency. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Completed) | ||
| Trial results: View results | ||
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