- Trials with a EudraCT protocol (6,332)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6,332 result(s) found for: 15 - 30.
Displaying page 93 of 317.
| EudraCT Number: 2019-004671-39 | Sponsor Protocol Number: 2019/318 | Start Date*: 2020-01-28 |
| Sponsor Name:Universitair Ziekenhuis Brussel (UZ Brussel) | ||
| Full Title: The effect of handheld-multimedia versus midazolam premedication on the level of perioperative anxiety in pediatric day-care. A randomized controlled trial. | ||
| Medical condition: Perioperative anxiety in children scheduled for an elective circumcision, dental care or tonsillectomy/adenoidectomy in day-care | ||
| Disease: | ||
| Population Age: Children, Under 18 | Gender: Male, Female | |
| Trial protocol: BE (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2024-000164-37 | Sponsor Protocol Number: LPS17250 | Start Date*: 2024-04-09 | |||||||||||
| Sponsor Name:Sanofi (China) Investment Co., Ltd, Shanhai Branch | |||||||||||||
| Full Title: Open-label exploratory study to evaluate the effect of dupilumab on skin barrier function in Chinese patients with moderate to severe atopic dermatitis | |||||||||||||
| Medical condition: Atopic Dermatitis | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-005299-36 | Sponsor Protocol Number: EXEVIR0101 | Start Date*: 2021-04-21 | |||||||||||
| Sponsor Name:ExeVir Bio BV | |||||||||||||
| Full Title: A 2-part Clinical Study Including a First-in-Human, Open-label, Single Ascending Dose Part (Phase 1) Followed by a Randomised, Double-blind, Placebo-controlled Part (Phase 2) to Evaluate the Effica... | |||||||||||||
| Medical condition: Subjects hospitalised for COVID 19 | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Prematurely Ended) PT (Prematurely Ended) IT (Prematurely Ended) RO (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002370-31 | Sponsor Protocol Number: IMA203-101 | Start Date*: 2020-03-10 | |||||||||||
| Sponsor Name:Immatics US InC | |||||||||||||
| Full Title: Phase 1/2 study evaluating genetically modified autologous T cells expressing a T-cell receptor recognizing a cancer/germline antigen as monotherapy or in combination with nivolumab in patients wi... | |||||||||||||
| Medical condition: Recurrent and / or refractory solid tumors | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-002197-78 | Sponsor Protocol Number: APHP200011 | Start Date*: 2021-08-19 |
| Sponsor Name:Assistance Publique - Hôpitaux de Paris | ||
| Full Title: Antimicrobial Stewardship For Ventilator Associated Pneumonia in Intensive Care Acronym: ASPIC | ||
| Medical condition: ventilator associated neumonia in intensive care | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-001015-23 | Sponsor Protocol Number: APHP180668 | Start Date*: 2020-05-13 |
| Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | ||
| Full Title: Double blind, multicentric, randomized, placebo-controlled trial, evaluating the efficacy of 24-month of bezafibrate in primary sclerosing cholangitis with persistent cholestasis despite ursodeoxyc... | ||
| Medical condition: Adult patients with primary sclerosing cholangitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-001976-39 | Sponsor Protocol Number: GORTEC-2018-02 | Start Date*: 2018-12-14 | |||||||||||
| Sponsor Name:GORTEC | |||||||||||||
| Full Title: A phase II trial of radiotherapy-durvalumab without prophylactic neck irradiation in squamous cell carcinoma of the head and neck | |||||||||||||
| Medical condition: Untreated Squamous cell carcinoma : Oral cavity, oropharynx, hypopharynx or larynx | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-001816-39 | Sponsor Protocol Number: SANTAL | Start Date*: 2016-07-15 | |||||||||||
| Sponsor Name:GORTEC | |||||||||||||
| Full Title: Phase III randomized trial comparating concomittant administration of radiotherapy with cisplatin versus radiotherapy only for treatment of sinuses tumors and salivary glands | |||||||||||||
| Medical condition: | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) BE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-000680-74 | Sponsor Protocol Number: IC/LV/ACZ/PCHC | Start Date*: 2021-08-26 | |||||||||||
| Sponsor Name:Fundació Hospital Universitari Vall d'Hebron - Institut de Recerca (VHIR) | |||||||||||||
| Full Title: Multicenter, randomized, double-blind, comparative clinical trial to assess the efficacy of Zinc Acexamate versus a placebo in improving the prognosis of patients with advanced chronic liver diseas... | |||||||||||||
| Medical condition: compensated advanced chronic liver disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-003477-36 | Sponsor Protocol Number: KKS-303 | Start Date*: 2023-06-27 | ||||||||||||||||
| Sponsor Name:Justus-Liebig University Giessen - KKS Marburg-Giessen | ||||||||||||||||||
| Full Title: Safety and immunogenicity of SHIngrix VAccination in patients suffering from Psoriasis or Psoriatic arthritis (SHIVAP) | ||||||||||||||||||
| Medical condition: Psoriasis vulgaris and/or psoriatric arthritis | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-002300-12 | Sponsor Protocol Number: EPOS_ZKSJ0134 | Start Date*: 2021-12-20 | |||||||||||
| Sponsor Name:Friedrich Schiller University | |||||||||||||
| Full Title: Epirubicin for the Treatment of Sepsis & Septic Shock | |||||||||||||
| Medical condition: Patients with sepsis or septic shock, currently hospitalized at the Intensive Care Unit (ICU) or Intermediate Care (IMC) regardless where the sepsis was first diagnosed. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-000470-36 | Sponsor Protocol Number: SEP361-301 | Start Date*: Information not available in EudraCT | ||||||||||||||||
| Sponsor Name:Sunovion Pharmaceuticals Inc. | ||||||||||||||||||
| Full Title: A Randomized, Double-blind, Parallel-group, Placebo-controlled, Fixed-dose, Multicenter Study to Evaluate the Efficacy and Safety of SEP-363856 in Acutely Psychotic Subjects with Schizophrenia | ||||||||||||||||||
| Medical condition: Schizophrenia | ||||||||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BG (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2018-000915-26 | Sponsor Protocol Number: 000295 | Start Date*: 2019-05-10 | |||||||||||
| Sponsor Name:Ferring Pharmaceuticals A/S | |||||||||||||
| Full Title: A randomised, double-blind, placebo-controlled, proof-of-mechanism phase 2 trial investigating the effect of quinagolide extended-release vaginal ring on reduction of lesions assessed by high-resol... | |||||||||||||
| Medical condition: Deep infiltrating endometriosis, endometrioma and/or adenomyosis. | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: DE (Completed) DK (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2020-004748-27 | Sponsor Protocol Number: EPIDAURUS-2020 | Start Date*: 2022-04-21 | |||||||||||
| Sponsor Name:LMU University Hospital Munich | |||||||||||||
| Full Title: Escalated single platelet inhibition for one month plus direct oral anticoagulation in patients with atrial fibrillation and acute coronary syndrome undergoing percutaneous coronary intervention | |||||||||||||
| Medical condition: Patients with atrial fibrillation and ST-segment elevation myocardial infarction (STEMI) or non-ST-segment elevation myocardial infarction (NSTEMI) (biomarker -positive acute coronary syndrome) und... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2013-003931-30 | Sponsor Protocol Number: CBS-EAM-10d | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Hôpital Universitaire Des Enfants Reine Fabiola | |||||||||||||
| Full Title: A prospective open-label study on efficacy and tolerability of colloidal bismuth sub-citrate as adjunctive therapy to a combination of esomeprazole, amoxicillin and metronidazole for 10 days for He... | |||||||||||||
| Medical condition: Helicobacter pylory infection | |||||||||||||
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| Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-004957-62 | Sponsor Protocol Number: ET20-093 | Start Date*: 2021-09-09 |
| Sponsor Name:Centre Léon Bérard | ||
| Full Title: Immunotherapy in MSI/dMMR Tumors in perioperative setting | ||
| Medical condition: MSI/dMMR tumors or EBV+ gastric cancer | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FR (Trial now transitioned) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-000317-14 | Sponsor Protocol Number: RAD-GRIN-101 | Start Date*: 2022-11-28 | |||||||||||
| Sponsor Name:GRIN Therapeutics, Inc. | |||||||||||||
| Full Title: A Multicenter Study to Assess the Safety, Tolerability, Pharmacokinetics, and Effect on Seizures and Behavioral Symptoms of Multiple Individually Titrated Doses of Radiprodil in Children with GRIN-... | |||||||||||||
| Medical condition: gain of function (GoF) variants in the GRIN2B gene | |||||||||||||
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| Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) NL (Trial now transitioned) DE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-000559-28 | Sponsor Protocol Number: OCTO-062 | Start Date*: 2017-01-25 | |||||||||||
| Sponsor Name:University of Oxford | |||||||||||||
| Full Title: Randomised phase II Trial of olaparib, chemotherapy or olaparib and cediranib in patients with platinum–resistant ovarian cancer | |||||||||||||
| Medical condition: BRCA mutated platinum-resistant ovarian cancer | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-012324-83 | Sponsor Protocol Number: UZB-BN-09-001 | Start Date*: 2009-07-04 | |||||||||||
| Sponsor Name:Prof Bart Neyns | |||||||||||||
| Full Title: CeCil: A randomized, non-comparative phase II clinical trial of the effect of radiation therapy plus Temozolomide combined with Cilengitide or Cetuximab on the 1-year overall survival of patients w... | |||||||||||||
| Medical condition: Subjects with newly diagnosed glioblastoma, who have met all eligibility criteria for the CENTRIC study (EMD 121974-011 study, EudraCT 2007-004344-78) with the exception of NOT having a tumor with ... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-000741-13 | Sponsor Protocol Number: ISG-ARTICLE | Start Date*: 2021-05-14 |
| Sponsor Name:ITALIAN SARCOMA GROUP | ||
| Full Title: A Randomized & Observational phase II trial assessing the activity of TrabectedIn vs gemCitabine in patients with metastatic or locally advanced LEiomyosarcoma pretreated with conventional chemothe... | ||
| Medical condition: metastatic or locally advanced Leiomyosarcoma pretreated with conventional chemotherapy | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: IT (Trial now transitioned) | ||
| Trial results: (No results available) | ||
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