- Trials with a EudraCT protocol (55)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
55 result(s) found for: Starch.
Displaying page 1 of 3.
EudraCT Number: 2011-004906-12 | Sponsor Protocol Number: ASK-3-2011 | Start Date*: 2011-11-07 | |||||||||||
Sponsor Name:Erling Bjerregaard Pedersen, Medicinsk forskningsafsnit, Regionshospitalet Holstebro | |||||||||||||
Full Title: Effect of hydroxyethyl starch on renal handling of sodium and water, vasoactive hormones,biomarkers and the circulatory system in patients undergoing hip replacement surgery | |||||||||||||
Medical condition: Patients undergoing hip replacement in spinal anesthesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000729-24 | Sponsor Protocol Number: 1821 | Start Date*: 2007-05-15 |
Sponsor Name:University Hospital Linköping | ||
Full Title: Coagulation effect of four common plasma volume expanders | ||
Medical condition: Fluid/Plasma substitution during total hip replacement | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004273-88 | Sponsor Protocol Number: ASK-1-2011 | Start Date*: 2011-09-21 | |||||||||||
Sponsor Name:Erling Bjerregaard Pedersen, Medicinsk forskningsafsnit, Regionshospitalet Holstebro | |||||||||||||
Full Title: Effect of hydroxyethyl starch on renal handling of sodium and water, vasoactive hormones,biomarkers and the circulatory system in patients undergoing laparoscopic nephrectomy | |||||||||||||
Medical condition: Patients undergoing laparoscopic nefrectomy in generel anesthesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005920-16 | Sponsor Protocol Number: CHUB-930105 | Start Date*: 2012-02-06 |
Sponsor Name:Association Hospitalière CHU Brugmann | ||
Full Title: Prospective, controled, randomized, double blind monocentric study evaluating the efficacy of the basic component of colloids (corn versus potato) on perioperative blood losses in elective cardiac ... | ||
Medical condition: Elective cardiac surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-003321-99 | Sponsor Protocol Number: ANES002 | Start Date*: 2012-03-02 |
Sponsor Name:UZ Brussels | ||
Full Title: Comparison of Volulyte® versus Tetraspan® in patients undergoing cardiopulmonary bypass. | ||
Medical condition: coagulation status, colloid oncotic pressure (COP) and ion- and acid-base balance. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-018343-34 | Sponsor Protocol Number: 09P07 | Start Date*: 2011-10-25 | |||||||||||
Sponsor Name:Ludwigs Maximilians University | |||||||||||||
Full Title: Comparison of 6% Hydroxyethyl Starch and 5% Albumin for Volume Replacement Therapy in Patients Undergoing Cystectomy (CHART study) | |||||||||||||
Medical condition: Comparison of 6% Hydroxyethyl Starch and 5% Albumin for Volume Replacement Therapy in Patients Undergoing Cystectomy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003445-17 | Sponsor Protocol Number: BBG001 | Start Date*: 2009-05-12 |
Sponsor Name:Queen Mary, University of London | ||
Full Title: The probiotic Bifidobacterium breve strain BBG-01 admistered early to preterm infants to prevent infection, necrotising enterocolitis and death. | ||
Medical condition: Necrotising enterocolitis in the preterm baby Late-onset (>72h of age) blood stream infection in the preterm baby Death of preterm babies before discharge from hospital | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-005040-85 | Sponsor Protocol Number: HaHes | Start Date*: 2006-03-17 |
Sponsor Name:Department of Anesthesia, Div. of Cardiothoracic and Vascular Anesthesia, Medical University Vienna | ||
Full Title: Comparison of Albumin 5%, Hydroxyethyl Starch 130/0.4 (6%) and Ringer Lactate for volume replacement during cardiac surgery | ||
Medical condition: Intensive care patients after cardiac surgery requiring volume therapy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-000156-42 | Sponsor Protocol Number: NL35250.008.10 | Start Date*: 2011-04-19 |
Sponsor Name:Amphia Hospital | ||
Full Title: Effect of the plasma substitutes Gelofusine and Hydroxyethyl Starch 130/0.4 combined with lactated ringer's solution on the coagulation system | ||
Medical condition: A standard component of the priming which is used in extra corporal circulation is the synthetic colloïd Gelofusine (Braun, Melsung AG, Germany). Because of logistical reasons and cost saving the q... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-002096-16 | Sponsor Protocol Number: 01/04 | Start Date*: 2005-05-23 |
Sponsor Name:Universitätskinderklinik Innsbruck | ||
Full Title: Effect of plasma volume expansion with hydroxy-ethyl-starch (HES) 130/0.4 or crystalloids on interstitial fluid accumulation and blood pressure in newborn infants with arterial hypotension | ||
Medical condition: Arterial hypotension | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2011-004274-28 | Sponsor Protocol Number: ASK-2-2011 | Start Date*: 2011-09-21 | |||||||||||
Sponsor Name:Erling Bjerregaard Pedersen, Medicinsk forskningsafsnit, Regionshospitalet Holstebro | |||||||||||||
Full Title: Effect of hydroxyethyl starch on renal handling of sodium and water, vasoactive hormones,biomarkers and the circulatory system in patients undergoing radical prostatectomy | |||||||||||||
Medical condition: Patients undergoing radical prostatectomy in generel anesthesia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001610-14 | Sponsor Protocol Number: 01072004 | Start Date*: 2005-03-21 |
Sponsor Name:Univ. hospital, Dpt. of anaesthesia | ||
Full Title: Effects of colloids on hemostasis in paediatric anaesthesia | ||
Medical condition: The aim of the study is to measure the effects of intraoperatively infused hydroxy-ethyl-starch and gelatin-solution on the coagulation system (fibrinpolymerisation and thrombingeneration) of infan... | ||
Disease: | ||
Population Age: Newborns, Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-001282-13 | Sponsor Protocol Number: AGO/2015/004 | Start Date*: 2015-06-30 |
Sponsor Name:Ghent University Hospital | ||
Full Title: Evaluation of acute normovolemic hemodilution on coagulation during liver surgery. | ||
Medical condition: coagulation during liver surgery Acute normowolemic hemodilution | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-011007-23 | Sponsor Protocol Number: CSBR759A2305 | Start Date*: 2009-07-21 | |||||||||||
Sponsor Name:NOVARTIS FARMA | |||||||||||||
Full Title: A facilitated access open-label, non-randomized, multicenter, long-term safety and efficacy study in Chronic Kidney Disease patients treated with SBR759 who have completed previous SBR759 studies | |||||||||||||
Medical condition: Hyperphosphataemia in patients with Chronic Kidney Disease (CKD) on haemodialysis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) GB (Prematurely Ended) SE (Prematurely Ended) FI (Prematurely Ended) FR (Prematurely Ended) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006097-15 | Sponsor Protocol Number: CSBR759A2304 | Start Date*: 2009-05-27 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: A double-blind, randomized, placebo-controlled multi-center trial to compare the phosphate lowering efficacy of different doses of SBR759 to placebo | ||||||||||||||||||
Medical condition: hyperphosphataemia in chronic kidney disease patients on renal replacement therapy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: LT (Prematurely Ended) BE (Completed) IT (Prematurely Ended) CZ (Prematurely Ended) HU (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-002176-27 | Sponsor Protocol Number: HC-G-H-1505 | Start Date*: 2017-08-30 | |||||||||||
Sponsor Name:Fresenius Kabi Deutschland GmbH | |||||||||||||
Full Title: Pragmatic, prospective, randomized, controlled, double-blind, multicentre, multinational study on the safety and efficacy of a 6% Hydroxyethyl starch (HES) solution versus an electrolyte solution ... | |||||||||||||
Medical condition: Hypovolaemia due to acute blood loss in trauma surgery | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) CZ (Completed) NL (Completed) ES (Restarted) FR (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-004541-34 | Sponsor Protocol Number: 21092005 | Start Date*: 2006-02-14 |
Sponsor Name:South Manchester University Healthcare Trust | ||
Full Title: The Effect of Enteral Administration of Synbiotics Upon Infection Rates in Major Burns | ||
Medical condition: Major burn injuries: Thermal related trauma with burn injury involving significant proportions of the total body surface area, as defined by age: Adults (>=17 years old): >= 15% body surface area ... | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2007-000390-31 | Sponsor Protocol Number: HyperHAES-PÄD-CARDIO-02 | Start Date*: 2007-10-30 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: Application of hypertonic hyperoncotic solutions for improvement of cardiac output after open heart surgery in children - monocentric, randomised, placebo controlled, double-blind clinical trial (p... | |||||||||||||
Medical condition: Children after open-heart surgery for congenital cardiac disease | |||||||||||||
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Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014774-18 | Sponsor Protocol Number: 09063 | Start Date*: 2009-10-29 |
Sponsor Name:University of Nottingham | ||
Full Title: The effects of balanced and unbalanced crystalloids and colloids on serum biochemistry and visceral blood flow: A two-phase, double-blind, randomised cross-over study | ||
Medical condition: This is a healthy volunteer study investigating the effect of balanced and unbalanced fluid infusions on serum electrolytes, osmolality and acid/base balance. In addition we are examining the role ... | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-009893-28 | Sponsor Protocol Number: 16012009 | Start Date*: 2009-04-15 | |||||||||||
Sponsor Name:HUCH, ATEK, TÖÖLÖN SAIRAALA, NEUROKIRURGIAN KLINIKKA | |||||||||||||
Full Title: Tavoite-ohjattu nestehoito vatsa-asennon neurokirurgisen potilaan anestesiassa | |||||||||||||
Medical condition: Kaula- ja lannerangan leikkauspotilaat. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: View results |
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