- Trials with a EudraCT protocol (48)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
48 result(s) found for: Echography.
Displaying page 1 of 3.
EudraCT Number: 2020-000749-15 | Sponsor Protocol Number: NL73142.068.20 | Start Date*: 2020-08-26 |
Sponsor Name:Academisch ziekenhuis Maastricht | ||
Full Title: Resolution Enhancement by a Supplemental Open-Label Venoactive drug for Eight weeks in Deep Vein Thrombosis | ||
Medical condition: Post-thrombotic syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005950-57 | Sponsor Protocol Number: 2005-07 | Start Date*: 2007-03-23 |
Sponsor Name:French Society of Cardiology | ||
Full Title: Assessment of Endothelial VAsomotricity after treatment by Nicotinic Acid in Patients presenting a recent Acute Coronary Syndrome | ||
Medical condition: acute coronary syndrome under 7 days | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005289-31 | Sponsor Protocol Number: LF-PB/14/05 | Start Date*: 2015-08-04 | |||||||||||
Sponsor Name:CHEMI S.P.A. | |||||||||||||
Full Title: A multicentre, double blind, randomized placebo controlled trial to assess the effect of LF-PB on seroma formation in women with breast cancer undergoing Axillary Lymph Node Dissection | |||||||||||||
Medical condition: Woman with Breast Cancer Undergoing Axillary Lymph Node Dissection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004787-62 | Sponsor Protocol Number: DUS | Start Date*: 2014-11-26 | |||||||||||
Sponsor Name:SOD Anestesia e Terapia Intensiva, DAI Oncologia, AOU Careggi, Firenze | |||||||||||||
Full Title: Evaluation of muscle function recovery after deep neuromuscular blockade by acceleromyography of the adductor pollicis or diaphragmatic echography: comparison between sugammadex and neostigmine | |||||||||||||
Medical condition: Muscle function recovery post neuromuscoular blockade | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003739-40 | Sponsor Protocol Number: 59153 | Start Date*: 2017-03-06 |
Sponsor Name:AMC Amsterdam | ||
Full Title: The effect of Iberogast on heartburn in patients with dyspepsia | ||
Medical condition: Dyspepsia (according to the Rome III criteria) with heartburn. Upper gastro-intestinal causes of the complaints excluded via gastroscopy | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-004125-24 | Sponsor Protocol Number: NL6979 | Start Date*: 2020-07-02 |
Sponsor Name:UMCG | ||
Full Title: Reduced Anticoagulation Targets in Extracorporeal life support | ||
Medical condition: Heart or lungfailure treated with ECMO | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005886-19 | Sponsor Protocol Number: HGKKRWPHD2 | Start Date*: 2012-07-31 | ||||||||||||||||||||||||||
Sponsor Name:Gastroenterology MIDT | ||||||||||||||||||||||||||||
Full Title: Correlation between intestinal blOod flow assessed by magNetic resonance imaging and ulTRASound Techniques (CONTRAST) | ||||||||||||||||||||||||||||
Medical condition: Crohns Disease with active disease | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-004942-12 | Sponsor Protocol Number: Protokol_MFCN_10102020 | Start Date*: 2020-11-19 | |||||||||||||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||||||||||||
Full Title: Selective ultrasound-guided nerve block of the medial femoral cutaneous nerve in healthy volunteers | |||||||||||||||||||||||
Medical condition: Pain around the surgical incisions after total knee arthroplasty (TKA). The area anesthetized by new nerve block techniques anesthetizing the medial femoral cutaneous nerve are investigated in heal... | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-005919-24 | Sponsor Protocol Number: C/399/2002 | Start Date*: 2006-07-19 |
Sponsor Name:Dr. Falk Pharma Portugal | ||
Full Title: Randomized, multicenter, double blind, placebo controlled trial, for the evaluation of the efficacy and tolerability of ursodeoxycholic acid on the dissolution of cholesterol gallstones (<15mm) aft... | ||
Medical condition: Randomized multicenter double blind, placebo controlled trial, for the evaluation of the efficacy and tolerability of UDCA on the dissolution of cholesterol gallstones (<15mm) after 18 months of th... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-005579-10 | Sponsor Protocol Number: A-93-52030-325 | Start Date*: 2016-02-26 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:IPSEN S.P.A. | |||||||||||||||||||||||||||||||||||||||||||
Full Title: EFFICACY AND SAFETY OF LANREOTIDE ATG 120 MG IN COMBINATION WITH TEMOZOLOMIDE IN SUBJECTS WITH PROGRESSIVE WELL DIFFERENTIATED THORACIC NEUROENDOCRINE TUMORS | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: progressive well differentiated thoracic neuroendocrine tumors | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-005426-18 | Sponsor Protocol Number: DECONGEST_v1.0 | Start Date*: 2022-03-02 | |||||||||||
Sponsor Name:UZ Brussel | |||||||||||||
Full Title: Diuretic Treatment in Acute Heart Failure with Volume Overload Guided by Serial Spot Urine Sodium Assessment | |||||||||||||
Medical condition: Acute Heart Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001576-30 | Sponsor Protocol Number: 15783408 | Start Date*: 2016-11-07 | |||||||||||
Sponsor Name:CHU TOULOUSE | |||||||||||||
Full Title: Interest of Intra-nodal injection of gentamicin for the treatment of suppurated cat scratch disease’s lymphadenitis: a randomized controlled study. "BIGG" : Bartonellosis and intra-nodal injection... | |||||||||||||
Medical condition: Bartonellosis | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003763-11 | Sponsor Protocol Number: CACZ885D2208 | Start Date*: 2016-06-15 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A 12-week, open-label, parallel-cohort study to evaluate the efficacy, safety and tolerability of canakinumab in pediatric IVIG-naïve or refractory patients with active Kawasaki disease | |||||||||||||
Medical condition: Active Kawasaki disease | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) BE (Completed) DE (Prematurely Ended) NL (Prematurely Ended) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004019-36 | Sponsor Protocol Number: Protocol 2-55-52030-729 | Start Date*: 2008-12-01 | |||||||||||
Sponsor Name:IPSEN Research and Development, BEAUFOUR IPSEN PHARMA | |||||||||||||
Full Title: Open label extension study of lanreotide Autogel 120 mg in patients with non functioning entero-pancreatic endocrine tumour. | |||||||||||||
Medical condition: Non functioning entero-pancreatic tumour | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) CZ (Completed) SK (Completed) BE (Completed) ES (Completed) PL (Completed) GB (Completed) SE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007727-41 | Sponsor Protocol Number: DTS-201CLI002 | Start Date*: 2008-04-29 | |||||||||||
Sponsor Name:Diatos S.A. | |||||||||||||
Full Title: An open-label, one arm, multi-centre Phase II trial evaluating the efficacy and safety of DTS-201 as a second-line chemotherapy in patients with hormone refractory prostate cancer | |||||||||||||
Medical condition: Hormone refractory prostate cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: FR (Ongoing) BE (Completed) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005844-26 | Sponsor Protocol Number: Cistcert | Start Date*: 2008-06-16 |
Sponsor Name:Antwerp University Hospital | ||
Full Title: Multicentre, prospective, randomized, open-label, controlled study in de novo kidney transplant recipients to evaluate the impact of cyclosporine or steroid withdrawal at 3 months on graft function... | ||
Medical condition: Preservation of renal function after kidney transplantation in a 5-year, multicentre, prospective, randomized, open-label, controlled study Patients will be randomized within 24 hours prior to tra... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003978-10 | Sponsor Protocol Number: INT/ISS 1 | Start Date*: 2006-10-31 | |||||||||||
Sponsor Name:ISTITUTO SUPERIORE DI SANITA' | |||||||||||||
Full Title: Pilot Study with fixed dose of Cisplatinum in combination with esomeprazole (dose-ranging) as salvage treatment in patients with pre-treated advanced/methastatic melanoma | |||||||||||||
Medical condition: Patient with metastatic melanoma (stage IV) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004160-38 | Sponsor Protocol Number: 93-8122-001 | Start Date*: 2015-04-01 |
Sponsor Name:KABI PHARMACIA S.A. | ||
Full Title: A 2 Year Multicenter Study of Genotropin Treatment of Short Prepubertal Children with Intra-Uterine Growth Retardation | ||
Medical condition: Growth Disorders, Intrauterine Growth Retardation | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2011-005846-36 | Sponsor Protocol Number: HGKKRWPHD | Start Date*: 2012-07-31 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Gastroenterology MIDT | ||||||||||||||||||||||||||||||||||||||
Full Title: Safe evaluation of obstructive crohns disease using bloodflow Time-intensity curves and Elastography correlated to Neutrocytes and collagen counts and biomechanical properties Obtained in Stenotic ... | ||||||||||||||||||||||||||||||||||||||
Medical condition: Crohns Disease undergoing elective surgery for intestinal stenosis. | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005487-13 | Sponsor Protocol Number: PLQ-002 | Start Date*: 2008-12-30 | |||||||||||
Sponsor Name:LEO Pharma A/S | |||||||||||||
Full Title: A plaque test comparing 4 steroids with Daivobet® ointment and a vehicle control for the treatment of psoriasis vulgaris | |||||||||||||
Medical condition: Psoriasis vulgaris lesions located on the arms, legs or trunk. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
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