- Trials with a EudraCT protocol (93)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (7)
93 result(s) found for: Calcium Channel.
Displaying page 1 of 5.
EudraCT Number: 2010-019469-26 | Sponsor Protocol Number: pRGF/016/09 | Start Date*: 2010-07-29 |
Sponsor Name:University of Aberdeen [...] | ||
Full Title: Use of drug therapy in the management of symptomatic ureteric stones in hospitalised adults: a multicentre placebo controlled randomised trial of a calcium channel blocker(nifedipine)and an alpha b... | ||
Medical condition: Use of drug therapy in the management of symptomatic ureteric stones in hospitalised adults: multicentre placebo controlled randomised trial of a calcium channel blocker(nifedipine) and an alpha bl... | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001761-11 | Sponsor Protocol Number: 300488 | Start Date*: 2015-08-31 | ||||||||||||||||
Sponsor Name:The Department of Cardiothoracic and Vascular Surgery, Aarhus University Hospital | ||||||||||||||||||
Full Title: Lymphatic dysfunction as a cause of calcium channel blocker oedema in post-menopausal women | ||||||||||||||||||
Medical condition: Calcium channel antagonist induced peripheral edema in post-menopausal women. We hypothesize that this condition is partly due to impaired lymphatic function in these patients. | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-001998-25 | Sponsor Protocol Number: BLO K025 | Start Date*: 2006-09-29 | |||||||||||
Sponsor Name:Takeda Pharma GmbH | |||||||||||||
Full Title: Double-blind, randomised trial to investigate the antihypertensive and metabolic effects of candesartan in insulin-resistant obese patients with a hypertension not adequately controlled by previous... | |||||||||||||
Medical condition: Insulin-resistant obese patients with a hypertension not adequately controlled by previous beta-blocker or calcium channel blocker | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002622-75 | Sponsor Protocol Number: 2013 | Start Date*: 2013-05-21 | ||||||||||||||||
Sponsor Name:Vibeke Hjortdal | ||||||||||||||||||
Full Title: Lymphatic dysfunction as a cause of calcium channel blocker oedema | ||||||||||||||||||
Medical condition: Fluid accumulation in the leg associated with calcium channel blocker therapy. | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000605-12 | Sponsor Protocol Number: notapplicable1 | Start Date*: 2014-06-13 |
Sponsor Name: | ||
Full Title: Thiazide diuretics versus calcium channel blockers for the treatment of calcineurin inhibitor-induced hypertension in patients with psoriasis or eczema: a single-center randomized cross-over trial. | ||
Medical condition: Hypertension, induced by the use of a Calcineurin Inhibitor (CNI) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004704-35 | Sponsor Protocol Number: NL39417.078.12 | Start Date*: 2012-11-22 |
Sponsor Name: | ||
Full Title: Thiazide diuretics versus calcium channel blockers for the treatment of tacrolimus-induced hypertension in dermatology patients: a single-center randomized cross-over trial. | ||
Medical condition: Hypertension, induced by the use of a Calcineurin Inhibitor (CNI) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003143-23 | Sponsor Protocol Number: MVH1 | Start Date*: 2007-02-12 |
Sponsor Name:St Radboud UMC | ||
Full Title: To study the cardiovasculair effects of vasodilatation by nifedipine (Adalat gastrointestinal therapeutic system) with or without plasma volume expansion with Voluven (colloid) in women with preecl... | ||
Medical condition: preeclampsia | ||
Disease: | ||
Population Age: | Gender: Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2006-003998-27 | Sponsor Protocol Number: RD-5103-003-06 | Start Date*: 2007-03-15 |
Sponsor Name:Derby Hospitals NHS Foundation Trust | ||
Full Title: Cardiovascular and functional consquences of chronic kidney disease in older people | ||
Medical condition: Chronic Kidney Disease Hypertension Falls | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-023938-23 | Sponsor Protocol Number: Antrorect/02/09 | Start Date*: 2011-01-12 | |||||||||||
Sponsor Name:BRACCO | |||||||||||||
Full Title: Effect of Mesalazine plus nifedipine suppositoires (Antrorect) in functional ano-rectal pain disorders: a pilot randomized double-blind placebo-controlled study. | |||||||||||||
Medical condition: Functional ano-rectal pain disorders | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005432-32 | Sponsor Protocol Number: 08.0113 | Start Date*: 2009-06-02 | |||||||||||
Sponsor Name:St. George's University of London (SGUL) | |||||||||||||
Full Title: Effects of an Angiotensin Receptor Antagonist Candesartan versus a calcium channel blocker Amlodipine on Microvascular Rarefaction, Endothelial Dysfunction and Microalbuminuria in Essential Hyperte... | |||||||||||||
Medical condition: Essential hypertension | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002010-35 | Sponsor Protocol Number: TinnEx | Start Date*: 2006-12-14 |
Sponsor Name:Prof. Herta Flor, Head of the Institute of Clinical and Cognitive Neuroscience | ||
Full Title: An Extinction Training in Tinnitus | ||
Medical condition: The effect of pregabalin on the success to reduce the interference by tinnitus by an extinction training is tested in chronic tinnitus sufferers. | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-001250-91 | Sponsor Protocol Number: GV-002.001 | Start Date*: 2005-10-04 |
Sponsor Name:GenVec, Inc. | ||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study Evaluating the Efficacy of BIOBYPASS® (ADGVVEGF121.10NH) Delivered by NOGA-Guided/MYOSTAR Catheter in "No Option" Patients with Cla... | ||
Medical condition: Moderate to severe angina pectoris due to advanced coronary artery disease (CAD). | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) AT (Completed) DE (Completed) GB (Completed) BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004192-37 | Sponsor Protocol Number: CRO1749 | Start Date*: 2012-04-24 | |||||||||||
Sponsor Name:Joint Research Compliance Office, Imperial College | |||||||||||||
Full Title: Hellenic Anglo Research into Morning Or Night antihypertensive drug deliverY trial. | |||||||||||||
Medical condition: Hypertension | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-000407-16 | Sponsor Protocol Number: 2197944/202 | Start Date*: 2013-07-24 | |||||||||||
Sponsor Name:Convergence Pharmaceuticals Ltd | |||||||||||||
Full Title: A randomised three week double-blind crossover study to compare the efficacy and safety of CNV2197944 75 mg tid versus placebo in the treatment of neuropathic pain in patients with diabetic periphe... | |||||||||||||
Medical condition: Neuropathic pain associated with diabetic peripheral neuropathy | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) BG (Completed) PL (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2010-019009-40 | Sponsor Protocol Number: A7331010 | Start Date*: 2010-07-08 | |||||||||||
Sponsor Name:Pfizer, S.A. | |||||||||||||
Full Title: Estudio clínico de Fase 2A, multicéntrico aleatorizado, doble ciego, controlado con placebo y con un fármaco activo, de diseño cruzado con dos cohortes y dos dosis, para la evaluación de la eficaci... | |||||||||||||
Medical condition: Tratamiento del vasospasmo en el fenómeno de Raynaud primario y secundario. | |||||||||||||
|
|||||||||||||
Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) SE (Completed) CZ (Completed) DE (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006981-40 | Sponsor Protocol Number: hypertension2006-006981-40 | Start Date*: 2007-05-03 | |||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust jointly with University of Cambridge | |||||||||||||
Full Title: Does the underlying haemodynamic abnormality determine response to antihypertensive therapy in patients with hypertension? | |||||||||||||
Medical condition: Essential hypertension | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) EE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005887-14 | Sponsor Protocol Number: B1321003 | Start Date*: 2010-01-12 | |||||||||||
Sponsor Name:Pfizer Ltd. | |||||||||||||
Full Title: A PHASE 3, MULTI-CENTER, RANDOMIZED, DOUBLE-BLIND, EFFICACY AND SAFETY STUDY OF MONOTHERAPY SITAXSENTAN SODIUM VERSUS COMBINATION THERAPY WITH SITAXSENTAN SODIUM AND SILDENAFIL CITRATE IN SUBJECTS ... | |||||||||||||
Medical condition: Pulmonary Arterial Hypertension | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) SK (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002809-48 | Sponsor Protocol Number: CRO782 | Start Date*: 2013-04-17 | |||||||||||
Sponsor Name:Imperial College London and Imperial College Healthcare NHS Trust | |||||||||||||
Full Title: Investigation of the safety and feasibility of AAV1/SERCA2a gene transfer in patients with chronic heart failure and a left ventricular assist device | |||||||||||||
Medical condition: Advanced heart failure | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001584-77 | Sponsor Protocol Number: MEIN/10/Ran-PCI/005 | Start Date*: 2012-10-08 | |||||||||||
Sponsor Name:Menarini International Operations Luxembourg S.A. | |||||||||||||
Full Title: Effect of Ranolazine in ischemic patients with indication of staged interventional therapy | |||||||||||||
Medical condition: Stable Angina Pectoris | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023979-25 | Sponsor Protocol Number: 2010/353 | Start Date*: 2011-01-03 | ||||||||||||||||
Sponsor Name:Department of Nephrology | ||||||||||||||||||
Full Title: Role of renal and systemic vascular resistance for progression of chronic kidney disease | ||||||||||||||||||
Medical condition: We want to investigate whether increased vasodilitation ( angiotensin converting enzyme inhibitor and calcium channel blocker) compared to standard treatment ( beta-blocker and angiotensin convert... | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
Subscribe to this Search
To subscribe to the RSS feed for this search click here . This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here . This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
Query did not match any studies.