- Trials with a EudraCT protocol (44,393)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
44,393 result(s) found.
Displaying page 2,161 of 2,220.
| EudraCT Number: 2016-005186-31 | Sponsor Protocol Number: 01062017 | Start Date*: 2018-06-06 | ||||||||||||||||
| Sponsor Name:Department of Plastic Surgery, Breast and Burns Treatment | ||||||||||||||||||
| Full Title: Fat Grafting with Ex-Vivo Expanded Adipose-Derived Stem Cells for Breast Reconstruction Following Mastectomy | ||||||||||||||||||
| Medical condition: This study will include patients with genetic predisposition to development of breast cancer, who are offered prophylactic bilateral skin-sparring mastectomy. | ||||||||||||||||||
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| Population Age: Adults | Gender: Female | |||||||||||||||||
| Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2008-005048-17 | Sponsor Protocol Number: VRP080415 | Start Date*: 2009-01-27 | ||||||||||||||||
| Sponsor Name:Verona Pharma Plc | ||||||||||||||||||
| Full Title: A Combined Clinical Phase I/IIa Study of the Safety and Efficacy of Nebulised RPL554 in Healthy Subjects, Allergic Asthmatics, and Allergic Rhinitics | ||||||||||||||||||
| Medical condition: Allergic Asthma and Allergic Rhinitis | ||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2020-003631-21 | Sponsor Protocol Number: CLNA043A12203 | Start Date*: 2021-06-28 | |||||||||||
| Sponsor Name:Novartis Pharma AG | |||||||||||||
| Full Title: A randomized, four-arm, canakinumab placebo-controlled, participant, investigator and sponsor-blinded study investigating the safety, tolerability and efficacy of intra-articular canakinumab follow... | |||||||||||||
| Medical condition: osteoarthritis | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) CZ (Prematurely Ended) HU (Prematurely Ended) EE (Completed) LT (Completed) LV (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000998-68 | Sponsor Protocol Number: 1.0 | Start Date*: 2013-07-02 | ||||||||||||||||
| Sponsor Name:Medizinische Universität Wien, Abteilung für Anästhesie und Intensivmedizin | ||||||||||||||||||
| Full Title: Advanced antibiotic prophylaxis for optimal perioperative protection during coronary artery bypass grafting | ||||||||||||||||||
| Medical condition: antibiotic prophylaxis during cardiac surgery | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: AT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2011-001332-29 | Sponsor Protocol Number: IFX2.0 | Start Date*: 2013-12-02 | ||||||||||||||||
| Sponsor Name:Universitätsklinik für Innere Medizin III, Klinische Abteilung für Gastroenterologie und Hepatologie | ||||||||||||||||||
| Full Title: Pharmacokinetics of Infliximab | ||||||||||||||||||
| Medical condition: Inflammatory bowel disease (Ulcerative Colitis, Crohn's disease) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: AT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2014-000570-19 | Sponsor Protocol Number: TBE_obesity_1.1 | Start Date*: 2014-07-11 |
| Sponsor Name:Institute of Specific Prophylaxis and Tropical Medicine | ||
| Full Title: Applikation of FSME-IMMUN® in obese persons | ||
| Medical condition: Studies have shown that obesity has a direct effect on the immune system and leads to immunosuppression, which leads to a susceptibility to infection. The aim of this study is to clarify if a modif... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-003244-76 | Sponsor Protocol Number: Prot-HIPEC-Ovar-201201.7 | Start Date*: 2014-07-11 |
| Sponsor Name:Medical University of Vienna | ||
| Full Title: Feasibility of intraoperative hyperthermic intraperitoneal chemotherapy with carboplatin and paclitaxel in patients with advanced epithelial ovarian cancer – a combined phase I / II trial | ||
| Medical condition: Otherwise treatment-naive patients with epithelial ovarian cancer, FIGO III - IVa | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-002949-38 | Sponsor Protocol Number: CVL-751-PD-001 | Start Date*: 2020-02-06 |
| Sponsor Name:Cerevel Therapeutics, LLC | ||
| Full Title: A PHASE 3, DOUBLE-BLIND, RANDOMIZED, PLACEBO CONTROLLED, PARALLEL GROUP, 27 WEEK TRIAL TO EVALUATE THE EFFICACY, SAFETY, AND TOLERABILITY OF TWO FIXED DOSES OF TAVAPADON IN EARLY PARKINSON’S DISEAS... | ||
| Medical condition: Patients (18 to 60 years age) who have diagnosis of Parkinson's Disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: HU (Prematurely Ended) CZ (Completed) DE (Completed) FR (Completed) PL (Completed) ES (Ongoing) BG (Completed) IT (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2008-006411-20 | Sponsor Protocol Number: CHUBX 2008/20 | Start Date*: 2009-02-13 | |||||||||||
| Sponsor Name:CHU de Bordeaux | |||||||||||||
| Full Title: EVALUATION PRONOSTIQUE DE LA TOMOGRAPHIE PAR EMISSION DE POSITONS COUPLEE AU SCANNER (TEP-TDM) AU FLUOROMISONIDAZOLE MARQUE AU FLUOR 18 (18F-FMISO) DANS LES CANCERS EPIDERMOIDES DES VOIES AERODIGES... | |||||||||||||
| Medical condition: CANCERS EPIDERMOIDES DES VOIES AERODIGESTIVES SUPERIEURES | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-003483-32 | Sponsor Protocol Number: FILO | Start Date*: 2019-04-25 |
| Sponsor Name:FILO | ||
| Full Title: BLINAtumomab after R-CHOP debulking therapy for patients with Richter Transformation. | ||
| Medical condition: Richter transformation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2004-004723-35 | Sponsor Protocol Number: SEVO-DIP | Start Date*: 2005-01-27 | |||||||||||
| Sponsor Name:OSPEDALE S. RAFFAELE DI MILANO | |||||||||||||
| Full Title: PRECONDITIONING EFFECT OF INALATORY ANESTHETICS | |||||||||||||
| Medical condition: SEVOFLURANE USED AS ANESTETIC IN ORDER TO OBTAIN A MYOCARDIAL PROTECTION | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-004721-41 | Sponsor Protocol Number: CHUBX 2008/08 | Start Date*: 2008-10-07 | |||||||||||
| Sponsor Name:CHU de Bordeaux | |||||||||||||
| Full Title: Profil des populations leucocytaires chez les patients atteints de psoriasis répondeurs et non répondeurs au traitement par efaluzimab (anti-CD11A) : étude systémique et cutanée | |||||||||||||
| Medical condition: patients atteints de psoriasis modérés à sévère | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Ongoing) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005020-38 | Sponsor Protocol Number: KF7039-02 | Start Date*: 2022-07-12 | |||||||||||
| Sponsor Name:Grünenthal GmbH | |||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled, Phase III trial to evaluate the efficacy and safety of a single intra-articular injection of RTX-GRT7039 in adult subjects with pain associated with ... | |||||||||||||
| Medical condition: Moderate to severe pain associated with osteoarthritis of the knee | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) DK (Completed) PT (Completed) BG (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-004282-25 | Sponsor Protocol Number: CHUBX2014/10 | Start Date*: 2015-03-25 |
| Sponsor Name:CHU de Bordeaux | ||
| Full Title: Subcutaneous route and pharmacology of metoclopramide - SOPHA-Méto | ||
| Medical condition: Digestive disorder (Nausea and vomiting) in palliative care and oncology | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2017-000129-12 | Sponsor Protocol Number: PCYC-1143-CA | Start Date*: 2017-10-10 | |||||||||||
| Sponsor Name:Pharmacyclics LLC | |||||||||||||
| Full Title: Phase 3 Study of Ibrutinib in Combination with Venetoclax in Subjects with Mantle Cell Lymphoma | |||||||||||||
| Medical condition: Mantle Cell Lymphoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) DE (Completed) BE (Completed) HU (Completed) ES (Ongoing) NL (Completed) GR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-000348-24 | Sponsor Protocol Number: CVB2018-1 | Start Date*: 2018-06-11 | |||||||||||||||||||||||||||||||
| Sponsor Name:Department of Otorhinolaryngology, Head and Neck Surgery | |||||||||||||||||||||||||||||||||
| Full Title: Mesenchymal stem cells for radiation-induced hyposalivation and xerostomia in previous head and neck cancer patients (MESRIX-II) | |||||||||||||||||||||||||||||||||
| Medical condition: The trial will include participants with Xerostomia (International Classification of Diseases-10: DQ 838A) who have been treated with raditherapy for a head and neck cancer prevoiusly. | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2015-000377-12 | Sponsor Protocol Number: CHUBX2014/26 | Start Date*: 2017-09-18 | ||||||||||||||||
| Sponsor Name:CHU de Bordeaux | ||||||||||||||||||
| Full Title: MISOBOLD - Prostate cancer hypoxia using BOLD MRI and 18F-FMISO PET imaging | ||||||||||||||||||
| Medical condition: Prostate cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Ongoing) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2019-001205-25 | Sponsor Protocol Number: EP0085 | Start Date*: 2025-04-25 |
| Sponsor Name:UCB Biopharma SRL | ||
| Full Title: An Open-Label, Multicenter, Follow-up Study to Evaluate the Long-Term Safety and Efficacy of Brivaracetam Used as Adjunctive Treatment in Subjects >=16 Years of Age With Partial Seizures With or Wi... | ||
| Medical condition: Epilepsy (partial seizures with or without secondary generalization) | ||
| Disease: | ||
| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
| Trial protocol: Outside EU/EEA | ||
| Trial results: View results | ||
| EudraCT Number: 2020-001943-21 | Sponsor Protocol Number: IFG-08-2019 | Start Date*: 2021-05-14 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Institut für Frauengesundheit GmbH | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: NeoOn – Neoadjuvant treatment of Ontruzant® (SB3) in patients with HER2-positive early breast cancer: An open-label, multicenter, phase IV study | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Female patients with early HER2positive breast cancer, neoadjuvantly treated. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2016-003143-11 | Sponsor Protocol Number: CHUBX201620 | Start Date*: 2016-10-27 | |||||||||||
| Sponsor Name:CHU de Bordeaux | |||||||||||||
| Full Title: Effect of intra-venous ocytocine injection after fetal expulsion in management of third-stage of labor after second trimester medical pregnancy termination | |||||||||||||
| Medical condition: second trimester medical pregnancy termination | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
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