- Trials with a EudraCT protocol (13)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
13 result(s) found for: Calculus.
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EudraCT Number: 2012-001924-37 | Sponsor Protocol Number: HJU1 | Start Date*: 2013-11-05 | |||||||||||
Sponsor Name:Fredericia Hospital | |||||||||||||
Full Title: Relaxation of the ureter during ureterorenoscopy | |||||||||||||
Medical condition: Elevated pressure in the upper urinary tract during ureterorenoscopy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001519-10 | Sponsor Protocol Number: ALN-GO1-008 | Start Date*: 2022-04-25 | |||||||||||
Sponsor Name:Alnylam Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy, Safety, Pharmacodynamics, and Pharmacokinetics of Lumasiran in Patients with Recurrent Calcium Oxalate Kidney Stone Di... | |||||||||||||
Medical condition: Recurrent calcium oxalate kidney stone disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004475-13 | Sponsor Protocol Number: 13.031 | Start Date*: 2014-03-05 | |||||||||||
Sponsor Name:Fredericia Hospital | |||||||||||||
Full Title: Pharmacological relaxation of the ureter when using access sheaths during ureterorenoscopy | |||||||||||||
Medical condition: Resistance in the ureter when inserting a ureteral access sheath during ureterorenoscopy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003962-24 | Sponsor Protocol Number: VEN1 | Start Date*: 2008-10-15 | |||||||||||
Sponsor Name:Fredericia hospital | |||||||||||||
Full Title: visceral pain originating from the upper urinary tract - a randomised controlled trial on the effect of morphine and oxycodone in patients undergoing percutaneus nephrolithotomy (PCNL) | |||||||||||||
Medical condition: kidney stone | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001364-30 | Sponsor Protocol Number: BBH-TQL-LC | Start Date*: 2013-07-22 | |||||||||||
Sponsor Name:Bispebjerg Hospital | |||||||||||||
Full Title: Ultrasoundguided transmuscular quadrates lumborum block after elective laparoscopic cholecystectomy. A prospective, randomised clinical trial. | |||||||||||||
Medical condition: Postoperative pain following laparoscopic cholecystectomy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005135-15 | Sponsor Protocol Number: 8101 colloidAug08 | Start Date*: 2009-01-12 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University of Nottingham | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Do 100 kiloDaltons matter? A prospective randomised double-blind study on the blood volume expanding effects of two different colloids in patients undergoing laparoscopic cholecystectomy | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients undergoing laparoscopic cholecystectomy | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-004013-25 | Sponsor Protocol Number: IMBE-01/2015 | Start Date*: 2016-09-20 | |||||||||||
Sponsor Name:Institute of Molecular Medicine and Biomedical Research- I.M.B.E. | |||||||||||||
Full Title: Mirabegron in the management of lower urinary tract symptoms (LUTS) related to double-J (JJ) ureteral stents. | |||||||||||||
Medical condition: Insertion of a JJ stent, prior to extracorporal shock wave lithotripsy (ESWL) and post ureterolithotripsy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003328-35 | Sponsor Protocol Number: CHD062-13 | Start Date*: 2014-03-13 | |||||||||||
Sponsor Name:Centre Hospitalier Départemental Vendée | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002629-95 | Sponsor Protocol Number: 170188 | Start Date*: 2022-08-02 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Department of vascular surgery, Lillebaelt Hospital | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Cefuroxime and Piperacillin Concentrations in the Biliary System | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Infection in the biliary system such as cholecystitis and cholangitis both as acute infections and post-operative infections. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002068-42 | Sponsor Protocol Number: B14CS | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Advicenne | |||||||||||||
Full Title: Open label, multicentre study, evaluating the safety, tolerability, efficacy, compliance and the acceptability of alkalising treatments at long-term in patients with cystinuria | |||||||||||||
Medical condition: Cystinuria | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003027-15 | Sponsor Protocol Number: EFFI2021/01 | Start Date*: 2023-03-20 | |||||||||||
Sponsor Name:ITALFARMACO S.P.A. | |||||||||||||
Full Title: A multicentre, prospective, open-label, non-comparative study to evaluate menstrual bleeding typology, tolerability, and compliance during a monophasic hormonal contraceptive treatment with norgest... | |||||||||||||
Medical condition: Combined Oral Contraceptives (COC) | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002067-18 | Sponsor Protocol Number: B12CS-B13CS | Start Date*: 2018-12-11 | |||||||||||
Sponsor Name:Advicenne | |||||||||||||
Full Title: A multicentre, randomised, controlled versus placebo, double-blinded, 4 parallel arms, dose-ranging main study, to evaluate the efficacy, safety and tolerability and acceptability of repeated doses... | |||||||||||||
Medical condition: Cystinuria | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014862-25 | Sponsor Protocol Number: a004c | Start Date*: 2010-01-22 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Helsinki University Central Hospital | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Dexmedetomidine vs placebo in ERCP sedation | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: ERCP(Endoscopic retrograde cholangiopancreatography) | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: FI (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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