- Trials with a EudraCT protocol (124)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
124 result(s) found for: Work-up.
Displaying page 1 of 7.
EudraCT Number: 2012-003789-41 | Sponsor Protocol Number: Her2.5 | Start Date*: 2014-05-15 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: HER2-PET as a diagnostic tool in breast cancer patients with a clinical dilemma | ||
Medical condition: Metastatic breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Temporarily Halted) | ||
Trial results: View results |
EudraCT Number: 2018-004153-24 | Sponsor Protocol Number: NL62838.029.18 | Start Date*: 2019-07-30 |
Sponsor Name:Amsterdam UMC - location Vrije Universiteit Amsterdam | ||
Full Title: Tubal flushing with oil-based contrast during HSG in subfertile women: Is early flushing effective and cost-effective as compared to delayed flushing? | ||
Medical condition: The research population consists of infertile women aged between 18 and 39 years of age, who have a spontaneous menstrual cycle and with a perceived low risk for tubal pathology, undergoing fertili... | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-001031-72 | Sponsor Protocol Number: HP-POST-COVID | Start Date*: 2021-04-08 | |||||||||||
Sponsor Name:Aarhus University, The MR Research Center | |||||||||||||
Full Title: Metabolic MRI with hyperpolarized pyruvate in long-term COVID19 patients | |||||||||||||
Medical condition: Long-term COVID19 symptoms | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-003496-11 | Sponsor Protocol Number: EN3348-303 | Start Date*: 2012-02-08 | |||||||||||
Sponsor Name:Endo Pharmaceuticals Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Active-Controlled, Open-Label, Multicenter Study to Evaluate the Efficacy and Safety of EN3348 (MCC) as Compared with Mitomycin C in the Intravesical Treatment of Subjects wi... | |||||||||||||
Medical condition: BCG Recurrent or Refractory Non-Muscle Invasive Bladder Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Prematurely Ended) GB (Prematurely Ended) DE (Prematurely Ended) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002773-21 | Sponsor Protocol Number: 89Zr-TLX250-003 | Start Date*: 2019-04-10 |
Sponsor Name:TELIX International Pty Ltd | ||
Full Title: A confirmatory, prospective, open-label, multi-centre phase 3 study to evaluate diagnostic performance of 89Zirconium-labelled girentuximab(89Zr-TLX250) to non-invasively detect clear cell renal ce... | ||
Medical condition: Patients with an indeterminate renal mass (IRM) detected on contrast-enhanced abdominal MR imaging or equivalent standard of care imaging, clinically suspicious for renal cell carcinoma and schedul... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) GB (GB - no longer in EU/EEA) BE (Completed) ES (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2019-002968-27 | Sponsor Protocol Number: INTERMEDIATE-01 | Start Date*: 2020-02-18 | |||||||||||
Sponsor Name:Centre François Baclesse | |||||||||||||
Full Title: Multicentric phase III trial comparing two strategies in intermediate-risk differentiated thyroid cancer patients: Systematic radioiodine administration (3.7 GBq I131 after rhTSH) versus decision o... | |||||||||||||
Medical condition: Differentiated thyroid cancer - subgroup of patients with intermediate risk of postoperative residual disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000986-20 | Sponsor Protocol Number: 040 - 380 212 60 | Start Date*: 2005-12-14 |
Sponsor Name:Technical University of Munich [...] | ||
Full Title: The CORE Study (Chemotherapy or Endocrine Treatment first?) | ||
Medical condition: Patients with advanced breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-000910-39 | Sponsor Protocol Number: BRTR1 | Start Date*: 2018-12-13 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA UDINE | ||||||||||||||||||
Full Title: Efficacy of tranexamic acid in reducing post-operative bleeding in oncologic-reconstructive breast surgery | ||||||||||||||||||
Medical condition: Post-operative hematoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000074-51 | Sponsor Protocol Number: GBG 39 | Start Date*: 2005-05-03 |
Sponsor Name:GBG Forschungs GmbH | ||
Full Title: A multicenter phase II study to determine the efficacy of capecitabine as first line monochemotherapy in patients with HER2 negative, medium-risk, metastatic breast cancer | ||
Medical condition: patients with HER2 negative metastatic breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-001505-93 | Sponsor Protocol Number: P11-11 | Start Date*: 2013-12-19 | |||||||||||
Sponsor Name:Bioprojet Pharma | |||||||||||||
Full Title: A MULTI-CENTRE, SINGLE DOSE TRIAL TO EVALUATE PHARMACOKINETICS OF PITOLISANT (BF2.649) IN CHILDREN FROM 6 TO LESS THAN 18 YEARS WITH NARCOLEPSY | |||||||||||||
Medical condition: Narcolepsy | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006335-26 | Sponsor Protocol Number: Xe-long-COVID | Start Date*: 2022-03-04 | |||||||||||
Sponsor Name:Aarhus University | |||||||||||||
Full Title: Hyperpolarized xenon lung MRI in long-term COVID19 | |||||||||||||
Medical condition: Long COVID19 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000924-14 | Sponsor Protocol Number: S52549 | Start Date*: 2011-05-23 |
Sponsor Name:KU Leuven LRD | ||
Full Title: Development and validation of a sputum biomarker mRNA panel for the diagnostic work-up of asthma | ||
Medical condition: asthma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-003040-20 | Sponsor Protocol Number: MX39795 | Start Date*: 2018-06-20 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A phase II, randomized, active-controlled, multi-center study comparing the efficacy and safety of targeted therapy or cancer immunotherapy guided by genomic profiling versus platinum-based chemoth... | |||||||||||||
Medical condition: Cancer of Unknown Primary Site | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) AT (Completed) EE (Completed) IE (Completed) DE (Completed) CZ (Completed) FI (Completed) LV (Completed) HU (Completed) PL (Completed) FR (Completed) ES (Ongoing) BG (Completed) PT (Completed) HR (Completed) NO (Completed) NL (Completed) DK (Completed) CY (Prematurely Ended) IT (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000703-42 | Sponsor Protocol Number: ML 18742 | Start Date*: 2006-05-17 | |||||||||||
Sponsor Name:ROCHE | |||||||||||||
Full Title: A phase III randomized trial of trastuzumab continuation vs discontinuation in combination with 2nd-line chemotherapy after progression on a 1st-line trastuzumab-chemotherapy combination for HER2 ... | |||||||||||||
Medical condition: Metastatic breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003835-18 | Sponsor Protocol Number: GE-135-004 | Start Date*: 2009-04-21 |
Sponsor Name:GE Healthcare Ltd | ||
Full Title: A phase 2, open-label test-retest study to assess the reproducibility of quantitative measurements of 18F uptake by solid tumours using PET imaging following intravenous administration of AH111585 ... | ||
Medical condition: Adult subjects with solid primary or metastatic tumours 2 cm or more in diameter. Malignancies may include but are not limited to non-small cell lung cancer (NSCLC), renal cell carcinoma (RCC), gl... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-008382-35 | Sponsor Protocol Number: AIFA - FARM07YPBW | Start Date*: 2010-04-08 | |||||||||||
Sponsor Name:Azienda Ospedaliera di Perugia | |||||||||||||
Full Title: Open , multicenter, randomized trial comparing two therapeutic approaches for the treatment of invasive fungal infections in neutropenic onco-hematologic patients.Empiric vs. ``presumptive`` (pree... | |||||||||||||
Medical condition: opportunistic fungal infections in neutropenic onco-hematologic patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022730-91 | Sponsor Protocol Number: BR1-130 | Start Date*: 2011-10-14 | |||||||||||
Sponsor Name:Bracco Imaging S.p.A. | |||||||||||||
Full Title: Characterization of focal liver lesions with Sonovue(R)-enhanced ultrasound imaging: a phase III, intrapatient comparative study versus unenhanced ultrasound imaging using histology or combined ... | |||||||||||||
Medical condition: At least one focal liver lesion requiring further work-up for complete characterization. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-009356-20 | Sponsor Protocol Number: I-48-52030-223 | Start Date*: 2009-06-25 | |||||||||||
Sponsor Name:IPSEN NV | |||||||||||||
Full Title: A PHASE II/III, MULTI-CENTRE, PROSPECTIVE, EXPLORATORY, OPEN LABEL STUDY TO ASSESS THE EFFICACY AND SAFETY OF LANREOTIDE AUTOGEL 120 MG IN THE SYMPTOMATIC TREATMENT OF PATIENTS WITH REFRACTORY DIAR... | |||||||||||||
Medical condition: Refractory diarrhea | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000551-41 | Sponsor Protocol Number: IMPACT_Breast_6.3 | Start Date*: 2014-03-18 |
Sponsor Name:University Medical Center Groningen | ||
Full Title: Towards patient tailored cancer treatment supported by molecular imaging IMPACT: IMaging PAtients for Cancer drug selecTion – Metastatic Breast Cancer | ||
Medical condition: Metastatic Breast Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-002717-35 | Sponsor Protocol Number: P170920J | Start Date*: 2018-12-13 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HÔPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Non inferiority multicenter phase III randomized trial comparing preoperative chemotherapy only to chemoradiotherapy for locally advanced resectable rectal cancer (intergroup FRENCH-GRECCAR- PRODIGE) | |||||||||||||
Medical condition: Adults ≥ 18 years with middle or low locally advanced resectable rectal carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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