- Trials with a EudraCT protocol (175)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
175 result(s) found for: Perfusion CT.
Displaying page 1 of 9.
EudraCT Number: 2019-001843-37 | Sponsor Protocol Number: 52649 | Start Date*: 2019-08-06 | ||||||||||||||||||||||||||
Sponsor Name:Radboud University Medical Center | ||||||||||||||||||||||||||||
Full Title: Imaging of tumour microenvironment in patients with oropharyngeal head and neck squamous cell carcinoma using RGD PET/CT imaging. | ||||||||||||||||||||||||||||
Medical condition: The aim of this study is to assess differences in tumour microenvironment between HPV positive and HPV negative oropharyngeal head and neck squamous cell carcinoma using [68Ga]Ga-RGD2 PET/CT and p... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002609-31 | Sponsor Protocol Number: ISO-44-013 | Start Date*: 2012-01-27 | |||||||||||
Sponsor Name:Guerbet | |||||||||||||
Full Title: Diagnostic contribution of XENETIX® CT PERFUSION in pre-therapeutical assessment of hepatocellular carcinoma. | |||||||||||||
Medical condition: Subjects diagnosed for HCC and planned for surgery (tumorectomy, sectionectomy, segmentectomy, lobectomy or transplantation). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002858-29 | Sponsor Protocol Number: IOM/BRA/037 (incl. Amendment #2) | Start Date*: 2006-10-27 | |||||||||||
Sponsor Name:Bracco Imaging Deutschland GmbH | |||||||||||||
Full Title: A DOUBLE-BLIND INTER-INDIVIDUAL COMPARISON OF IOMEPROL 300 AND IOMEPROL 400 IN THE ASSESSMENT OF PERFUSION CT OF ADVANCED RENAL CARCINOMA | |||||||||||||
Medical condition: Indication for Computed tomography (Computerized tomography (CT MeDRA 9.0 LLT 10062404)) and Metastatic renal carcinoma (MeDRA 9.0 LLT 10050076) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001049-42 | Sponsor Protocol Number: | Start Date*: 2012-07-05 |
Sponsor Name:Department of Oncology, Rigshospitalet | ||
Full Title: MRI-perfusion and FLT- and FET-PET during bevacizumab monotherapy for patients with recurrent Glioblastoma Multiforme | ||
Medical condition: Recurrent Glioblastoma multiforme | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-002557-29 | Sponsor Protocol Number: SK_DMDPA-03 | Start Date*: 2021-10-25 | |||||||||||
Sponsor Name:Synektik Spółka Akcyjna | |||||||||||||
Full Title: A Phase III Study of [11C]-DMDPA Tracer for Positron Emission Tomography PET-CT Myocardial Perfusion Imaging (MPI). | |||||||||||||
Medical condition: Known or suspected acute coronary syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001869-32 | Sponsor Protocol Number: 24042019 | Start Date*: 2020-01-29 |
Sponsor Name:Radboudumc | ||
Full Title: Nano-MRI to visualize pancreatic inflammation in individuals with recent-onset type 1 diabetes | ||
Medical condition: Type 1 Diabetes | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-005451-20 | Sponsor Protocol Number: MMI_2020_35 | Start Date*: 2021-06-03 |
Sponsor Name:Fondation A. de Rothschild Hospital | ||
Full Title: REperfusion with P2Y12 inhibitors in addition to mEchanical thRombectomy for perFUsion imaging selected acute Stroke patiEnts : a multicentric randomized controlled trial | ||
Medical condition: patients with a clinical diagnosis of AIS consecutive to LVO between 0 and 24 hours of symptom onset and selected by perfusion imaging | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002833-20 | Sponsor Protocol Number: EP-TSC-663 | Start Date*: 2012-08-20 | ||||||||||||||||
Sponsor Name:Oxford University Hospitals NHS Trust | ||||||||||||||||||
Full Title: Prospective study of 18F-RGD PET-CT in assessment of response to antiangiogenic treatment in patients with renal cancer and comparison with perfusion CT | ||||||||||||||||||
Medical condition: Primary and metastatic cancer. The active substance is a diagnostic agent that identifies angiogenesis associated with tumour growth. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-000564-29 | Sponsor Protocol Number: SUGBG-013001 | Start Date*: 2013-04-25 |
Sponsor Name:Sahlgrenska University Hospital | ||
Full Title: The Scandinavian Randomized Controlled Trial of Isolated Hepatic Perfusion for Uveal Melanoma Liver Metastases | ||
Medical condition: Uveal melanoma liver metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2022-002720-12 | Sponsor Protocol Number: GDX-44-016 | Start Date*: 2023-03-20 | |||||||||||
Sponsor Name:Guerbet | |||||||||||||
Full Title: Performance of Elucirem® (gadopiclenol) in Dynamic Susceptibility Contrast Magnetic Resonance Imaging (DSC-MRI) perfusion of brain gliomas | |||||||||||||
Medical condition: Naive or recurrent primary glial tumor | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004299-24 | Sponsor Protocol Number: 1.0 | Start Date*: 2017-11-02 |
Sponsor Name:Erasmus MC Kanker Instituut | ||
Full Title: Adjuvant hepatic arterial infusion pump chemotherapy after resection of colorectal liver metastases in patients with a low clinical risk score - a feasibility study | ||
Medical condition: Patients with resectable colorectal liver metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-001696-21 | Sponsor Protocol Number: 1.0 | Start Date*: 2018-08-16 |
Sponsor Name:Erasmus MC Kanker Instituut | ||
Full Title: Adjuvant hepatic arterial infusion pump chemotherapy after resection of colorectal liver metastases in patients with a low clinical risk score - a randomized controlled trial | ||
Medical condition: Patients with resectable colorectal liver metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2008-008652-16 | Sponsor Protocol Number: BR1-129 | Start Date*: 2009-10-01 | |||||||||||
Sponsor Name:BRACCO IMAGING | |||||||||||||
Full Title: QUANTITATIVE EVALUATION OF SONOVUE ENHANCED ULTRASONOGRAPHY FOR EARLY IDENTIFICATION OF SUBJECTS WITH HEPATOCELLULAR CARCINOMA REFRACTORY TO SORAFENIB THERAPY : A PHASE II EXPLORATIVE, INTRA-PATIEN... | |||||||||||||
Medical condition: HCC epatocellular carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023120-24 | Sponsor Protocol Number: Nitro1 | Start Date*: 2011-10-18 | |||||||||||
Sponsor Name:MAASTRO clinic | |||||||||||||
Full Title: Nitroglycerin's effect on perfusion and hypoxia in human non small cell lung cancer: proof of principle, a phase II trial | |||||||||||||
Medical condition: non small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002657-36 | Sponsor Protocol Number: HMRI2012101/1 | Start Date*: 2015-11-13 | |||||||||||
Sponsor Name:University of Newcastle | |||||||||||||
Full Title: Tenecteplase versus Alteplase for Stroke Thrombolysis Evaluation (TASTE) Trial | |||||||||||||
Medical condition: Acute Ischaemic Stroke | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) SE (Prematurely Ended) FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003697-27 | Sponsor Protocol Number: CS2/713 | Start Date*: 2020-05-04 | |||||||||||
Sponsor Name:AOU CITTA' DELLA SALUTE E DELLA SCIENZA DI TORINO | |||||||||||||
Full Title: Effect of inhalatory sedation on cerebral perfusion in subarchnoid hemorrhage | |||||||||||||
Medical condition: Patients with non traumatic subarachnoid hemorrhage (WFNS = 3 -5) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004837-34 | Sponsor Protocol Number: STH17245 | Start Date*: 2014-08-20 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: Lung HeXeRT: Advanced proton, hyperpolarised 3helium and 129xenon magnetic resonance imaging for lung cancer radiotherapy planning and evaluation | |||||||||||||
Medical condition: Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002373-35 | Sponsor Protocol Number: T153/2016 | Start Date*: 2016-07-04 |
Sponsor Name: | ||
Full Title: The Effects of Dietary Peptides on Human Brown Adipose Tissue | ||
Medical condition: Healthy volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-005469-22 | Sponsor Protocol Number: TEMPO-2 | Start Date*: 2016-09-09 |
Sponsor Name:University of Calgary | ||
Full Title: Multi-Centre, prosepective randomised open label, blinded-endpoint (PROBE) controlled trial of thrombolysis with low dose Tenecteplase (TNK-tPA) versus standard of care in the prevention of disabil... | ||
Medical condition: To demonstrate the efficacy of using TNK-tPA (tenecteplase), a thrombolytic agent that is relatively novel to the treatment ischemic stroke but well-established in the treatment of myocardial inf... | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) IE (Prematurely Ended) ES (Completed) FI (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-004325-25 | Sponsor Protocol Number: MS325-19 | Start Date*: 2007-01-04 |
Sponsor Name:Administration management, Ludwig-Maximilians-University of Munich | ||
Full Title: Comprehensive whole-body 3T MRA of Patients with Low or Moderate Clinical Probability for Pulmonary Embolism using an Intravascular MR Contrast Agent Vasovist® | ||
Medical condition: Patients with low or moderate clinical probability for pulmonary embolism and positive or negative CTA for pulmonary embolism after CT and sonographic examination for deep venous thrombosis. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
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