- Trials with a EudraCT protocol (44,395)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
44,395 result(s) found.
Displaying page 1,663 of 2,220.
| EudraCT Number: 2019-000794-23 | Sponsor Protocol Number: 49RC19_0034 | Start Date*: 2019-07-26 | |||||||||||||||||||||
| Sponsor Name:CHU ANGERS | |||||||||||||||||||||||
| Full Title: AntiCoagulants et COGnition (essai ACCOG) : Essai contrôlé randomisé en simple aveugle comparant les effets neurocognitifs du rivaroxaban par rapport à un antagoniste de la vitamine K | |||||||||||||||||||||||
| Medical condition: fibrillation atriale non valvulaire | |||||||||||||||||||||||
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| Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: FR (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||
| EudraCT Number: 2020-001387-28 | Sponsor Protocol Number: NL73559.091.20 | Start Date*: 2020-06-22 | ||||||||||||||||
| Sponsor Name:Radboud University Medical Center | ||||||||||||||||||
| Full Title: 18F-PSMA-1007 PET to detect primary prostate cancer: a comparative study with mpMRI and correlation to histopathology. | ||||||||||||||||||
| Medical condition: 75 patients with the suspicion on PCa (elevated PSA and/or abnormal digital rectal exam) will receive a PSMA-PET following mpMRI. 25 patients with PIRADS 1-2 (probably benign disease), 25 patients ... | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||
| Trial protocol: NL (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-005347-79 | Sponsor Protocol Number: UMCN-AKF-21.07 | Start Date*: 2022-03-31 | ||||||||||||||||
| Sponsor Name:Radboud University Medical Center | ||||||||||||||||||
| Full Title: The influence of having bariatric surgery on the pharmacokinetics, safety and efficacy of the novel non-nucleoside reverse transcriptase inhibitor doravirine (LABRADOR) | ||||||||||||||||||
| Medical condition: HIV plus bariatric surgery | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2021-001802-30 | Sponsor Protocol Number: TMP-3001-2020-30 | Start Date*: 2021-10-28 |
| Sponsor Name:Fraunhofer Institut für Translationale Medizin und Pharmakologie (ITMP) | ||
| Full Title: Efficacy of belimumab to improve subclinical cardiovascular abnormalities using imaging endpoints with cardiac magnetic resonance in patients with systemic lupus erythematosus (BeCarma) | ||
| Medical condition: Efficacy of belimumab to improve subclinical cardiovascular abnormalities using imaging endpoints with cardiac magnetic resonance in patients with systemic lupus erythematosus | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-002507-18 | Sponsor Protocol Number: CSET2019/2955 | Start Date*: 2020-04-10 | ||||||||||||||||
| Sponsor Name:Gustave Roussy | ||||||||||||||||||
| Full Title: Efficacy and feasibility of pasireotide to reduce clinically relevant digestive leakage after complete cytoreductive surgery (CRS) plus Hyperthermic Intra-Peritoneal Chemotherapy (HIPEC) for perito... | ||||||||||||||||||
| Medical condition: Primary and secondary peritoneal malignancies | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2014-004501-32 | Sponsor Protocol Number: NL51240.018.14 | Start Date*: 2014-12-11 |
| Sponsor Name:Academic Medical Center | ||
| Full Title: Infusion VErsus STimulation, a cost-effectiveness analysis of the treatment in advanced Parkinson's disease comparing Continuous Intrajejunal Levodopa Infusion to the traditional standard treetment... | ||
| Medical condition: Patients with advanced PD who's motor symptoms — severe response fluctuations, dyskinesias, painful dystonia and / or bradykinesia — cannot be controlled despite optimal oral pharmacological therapy. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-002269-14 | Sponsor Protocol Number: NL80263.018.21 | Start Date*: 2022-08-11 |
| Sponsor Name:AMC, Cardiovascular Sciences | ||
| Full Title: Dotatate to locate coronary plaques at high-risk of myocardial infarction | ||
| Medical condition: Inflammatory atherosclerosis of the coronary arteries. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2019-000702-30 | Sponsor Protocol Number: 18.021 | Start Date*: 2019-10-30 | |||||||||||
| Sponsor Name:Odense University Hospital | |||||||||||||
| Full Title: Fibromyalgia and Naltrexone: The FINAL study | |||||||||||||
| Medical condition: Fibromyalgia | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-001917-35 | Sponsor Protocol Number: NOX66-005 | Start Date*: 2021-10-25 |
| Sponsor Name:Noxopharm Limited | ||
| Full Title: A Phase 1b/2a Multicenter Study of NOX66 and External Beam Radiotherapy in Patients with Metastatic Castration-resistant Prostate Cancer and Other Solid Tumors | ||
| Medical condition: Metastatic Castration-resistant Prostate Cancer and Other Solid Tumors | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: HU (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2019-000842-36 | Sponsor Protocol Number: Version128May2019 | Start Date*: 2020-04-07 | |||||||||||
| Sponsor Name:The Clatterbridge Cancer Centre NHS Foundation Trust | |||||||||||||
| Full Title: A Polatuzumab Vedotin Containing Chemo-Immunotherapeutic Regimen in Patients with Diffuse Large B-Cell Lymphoma Unsuitable for Full Dose R-CHOP Therapy | |||||||||||||
| Medical condition: Diffuse large B-cell lymphoma in patients with co-morbidities who cannot tolerate full dose R-CHOP. | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-002154-70 | Sponsor Protocol Number: CP40559 | Start Date*: 2019-10-24 | ||||||||||||||||||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||||||||||||
| Full Title: A MULTICENTER, SINGLE-ARM, OPEN-LABEL STUDY TO ASSESS THE SAFETY, PHARMACOKINETICS, AND EFFICACY OF BALOXAVIR MARBOXIL IN OTHERWISE HEALTHY PEDIATRIC PATIENTS FROM BIRTH TO LESS THAN 1 YEAR WITH IN... | ||||||||||||||||||||||||||||
| Medical condition: Influenza | ||||||||||||||||||||||||||||
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| Population Age: Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: PL (Completed) ES (Ongoing) FI (Completed) BG (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2020-003309-79 | Sponsor Protocol Number: MK-8591-024 | Start Date*: 2021-04-30 | |||||||||||
| Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Active-Controlled, Double-Blind Clinical Study to Evaluate the Efficacy and Safety of Oral Islatravir Once-Monthly as Preexposure Prophylaxis in Cisgender Men and Transgender... | |||||||||||||
| Medical condition: HIV Preexposure prophylaxis | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) Outside EU/EEA | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-000382-32 | Sponsor Protocol Number: REP0121 | Start Date*: 2021-08-16 | |||||||||||
| Sponsor Name:Dompé farmaceutici s.p.a. | |||||||||||||
| Full Title: A multicenter, randomized, double-blind, placebo-controlled phase 2 study to assess the efficacy and safety of oral reparixin in cancer related fatigue in patients with locally advanced or metastat... | |||||||||||||
| Medical condition: Cancer related fatigue in patients with locally advanced or metastatic breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-000307-26 | Sponsor Protocol Number: CeTMAd-VIH-2014 | Start Date*: 2016-06-09 | |||||||||||
| Sponsor Name:Iniciativa Andaluza en Terapias Avanzadas-Fundación Pública Andaluza Progreso y Salud | |||||||||||||
| Full Title: Clinical trial Phase I/II, test of concept, double blind, randomized, controlled with placebo, to evalue the safety and efficiency of the treatment with expanded adult mesenchymal stem cells from a... | |||||||||||||
| Medical condition: Infection for HIV with controlled viral load and immunological discordant response | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-001984-21 | Sponsor Protocol Number: 3/013/13 | Start Date*: 2013-09-11 | |||||||||||
| Sponsor Name:University of Aberdeen & NHS Grampian | |||||||||||||
| Full Title: PRE-EMPT: Preventing Recurrence of Endometriosis by Means of long acting Protestogen Therapy | |||||||||||||
| Medical condition: Endometriosis | |||||||||||||
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| Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2016-002638-54 | Sponsor Protocol Number: ALN-AS1-002 | Start Date*: 2017-12-20 | |||||||||||
| Sponsor Name:Alnylam Pharmaceuticals, Inc. | |||||||||||||
| Full Title: A Multicenter, Open-label Extension Study to Evaluate the Long-term Safety and Clinical Activity of Subcutaneously Administered ALN-AS1 in Patients with Acute Intermittent Porphyria who have Comple... | |||||||||||||
| Medical condition: Acute Intermittent Porphyria (AIP) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: SE (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2021-005596-39 | Sponsor Protocol Number: MPELONG | Start Date*: 2022-09-07 |
| Sponsor Name:MAPS Europe B.V. | ||
| Full Title: Long-Term Safety and Persistence of Effectiveness of Manualized MDMA Assisted Therapy for the Treatment of Posttraumatic Stress Disorder | ||
| Medical condition: post-traumatic stress disorder (PTSD) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2017-004037-93 | Sponsor Protocol Number: TRACE | Start Date*: 2018-01-17 |
| Sponsor Name:Afdeling for Rygkirurgi, Led- og Bindevævssygdomme ; Rigshospitalet - Glostrup | ||
| Full Title: TReat-to-tArget (T2T) with seCukinumab in axial spondyloarthritis. IdEntification of MRI and biochemical biomarkers for disease activity, treatment response and structural damage progression (the T... | ||
| Medical condition: Axial spondyloarthritis and ankylosing spondylitis | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DK (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2021-004600-17 | Sponsor Protocol Number: T21 | Start Date*: Information not available in EudraCT | |||||||||||
| Sponsor Name:Royal College of Surgeons in Ireland | |||||||||||||
| Full Title: The use of Sildenafil in Neonates with Down Syndrome to Reduce Pulmonary Vascular Resistance. | |||||||||||||
| Medical condition: to assess the impact of oral sildenafil administration on echocardiography measurements of pulmonary vascular resistance in neonates with Down Syndrome without Congenital Heart Disease. | |||||||||||||
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| Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-005544-79 | Sponsor Protocol Number: Beau_Resp_05_001 | Start Date*: 2006-03-24 |
| Sponsor Name:The Clinical Research Centre, RCSI Education and Research Centre | ||
| Full Title: Adalimumab (Humira) as add-on therapy in the treatment of patients with severe persistent therapy resistant asthma | ||
| Medical condition: Severe Asthma | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: IE (Prematurely Ended) | ||
| Trial results: View results | ||
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