- Trials with a EudraCT protocol (33)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
33 result(s) found for: Malnutrition.
Displaying page 1 of 2.
EudraCT Number: 2017-000530-54 | Sponsor Protocol Number: VS56151/17000277 | Start Date*: 2018-01-16 | |||||||||||||||||||||
Sponsor Name:University of Copenhagen | |||||||||||||||||||||||
Full Title: The effect of cannibinols in patients with pancreatic cancer in the palliative state | |||||||||||||||||||||||
Medical condition: Pancreatic cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000330-50 | Sponsor Protocol Number: EC07/90285 | Start Date*: 2008-10-27 | |||||||||||
Sponsor Name:Organisation name was not entered | |||||||||||||
Full Title: EFECTO DE SUPLEMENTACIÓN NUTRICIONAL ENRIQUECIDA CON ÁCIDOS GRASOS OMEGA-3 EN EL ESTRÉS OXIDATIVO Y METABOLISMO LIPÍDICO DE PACIENTES CON PROCESOS ONCOLÓGICOS DEL ÁREA OTORRINOLARINGOLÓGICA (ORL) ... | |||||||||||||
Medical condition: Determinar las modificaciones inducidas por la suplementación especifica de ácidos grasos omega3 en el estrés oxidativo y estado inflamatorio en pacientes oncológicos sometidos a tratamiento radiot... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002318-15 | Sponsor Protocol Number: 010921 | Start Date*: 2021-09-15 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Copenhagen University Hospital, Amager and Hvidovre, Department of Clinical Research | ||||||||||||||||||||||||||||||||||||||
Full Title: A pharmacological trial with Sativex® and gentamicin for optimized pharmacological treatment of older patients with a focus on appetite stimulation and renal risk drugs | ||||||||||||||||||||||||||||||||||||||
Medical condition: | ||||||||||||||||||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003899-13 | Sponsor Protocol Number: NL65803.078.18 | Start Date*: 2018-12-20 |
Sponsor Name: | ||
Full Title: The effect of IntraDialytic Parenteral Nutrition on nutritional status and quality of life in hemodialysis patients | ||
Medical condition: Malnutrition / Sarcopenia (loss of muscle mass) in hemodialyse patients. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-004150-17 | Sponsor Protocol Number: 341-15 | Start Date*: 2015-12-11 |
Sponsor Name:Västra Götalandsregionen | ||
Full Title: The Effect of Satiety Gut Hormone Modulation on Appetitive Drive After Upper Gastrointestinal Surgery | ||
Medical condition: Weight loss and malnutrition after curative surgery for upper gastrointestinal cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-006153-31 | Sponsor Protocol Number: CSC/P01/07/Mu.F | Start Date*: 2008-04-23 | |||||||||||
Sponsor Name:Baxter R and D Europe SCRL | |||||||||||||
Full Title: Safety and efficacy of subcutaneous (SC) administration of Clinimix N9G15E in elderly patients at risk for malnutrition, at a dose of 1 liter infused over 12 hours for 7 to 10 consecutive days. A p... | |||||||||||||
Medical condition: The population studied will be the elderly population at risk for malnutrition without any predefined pathology at hospital geriatrician wards. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001778-40 | Sponsor Protocol Number: VITAMINA_D | Start Date*: 2017-10-11 |
Sponsor Name:Leonor Cuadra Llopart | ||
Full Title: A Prospective Randomized Trial Comparing the Effect of 2 vitamin D supplementation regimens in elderly people after hip fracture surgery | ||
Medical condition: Hip fracture and vitamin D deficiency | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-000439-27 | Sponsor Protocol Number: CL0600-005 | Start Date*: 2007-10-29 |
Sponsor Name:NPS Allelix Corporation | ||
Full Title: A Study of the Safety and Efficacy of Teduglutide in Subjects with Parenteral Nutrition-Dependant Short Bowel Syndrome Who Completed Protocol CL0600-004 | ||
Medical condition: Short Bowel Syndrome (SBS) refers to the clinical situation whereby a significant reduction in the absorptive capacity of the intestine results from inadequate anatomical or functional length of re... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-002000-31 | Sponsor Protocol Number: FSJD-ISON-2016 | Start Date*: 2016-09-21 |
Sponsor Name:FUNDACIÓ SANT JOAN DE DÉU | ||
Full Title: Open clinical trial phase IIa to study the isoniazid suspension absoption of 10mg/ml for the tuberculosis infection treatment in patients under the age of 6 | ||
Medical condition: tuberculosis infection in patients under the age of 6 | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004080-70 | Sponsor Protocol Number: | Start Date*: 2011-11-17 |
Sponsor Name:Med. Univ. Wien, Universitätsklinik für Anästhesie, Allgemeine Intensivmedizin und Schmerztherapie | ||
Full Title: Preoperative parenteral thiamine supplementation in patients undergoing heart surgery – a pilot study | ||
Medical condition: The objective of this study is to determine the prevalence of thiamine deficiency (TD) in patients with heart surgery, to examine the association between thiamine levels and lactic acidosis and to ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003703-19 | Sponsor Protocol Number: 18-002 | Start Date*: 2020-04-20 |
Sponsor Name:RWTH Aachen University represented by the Rector himself, represented by the Dean of the Medical Faculty | ||
Full Title: The Effect of Higher Protein Dosing in Critically Ill Patients: A Multicenter Randomized Trial | ||
Medical condition: Nutritionally high-risk critically ill mechanically ventilated patients. In this sub-study, eligible and enrolled patients randomized to the high protein dose group will achieve its protein goals b... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2017-004406-18 | Sponsor Protocol Number: INRCA-2017-01 | Start Date*: 2019-02-14 | |||||||||||
Sponsor Name:IRCC INRCA | |||||||||||||
Full Title: Geriatric outcomes among older Type 2 diabetic patients treated with DPP4 inhibitors or glinides: focus on pro-inflammatory and oxidative stress markers (GOOD-WP1) | |||||||||||||
Medical condition: TYPE 2 DIABETES | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001941-25 | Sponsor Protocol Number: 2014-002 | Start Date*: 2014-12-16 | |||||||||||||||||||||
Sponsor Name:Rigshospitalet 2121 | |||||||||||||||||||||||
Full Title: Pilot Study with Treatment of Short Bowel Syndrome Patients with dipeptidyl-peptidase 4 inhibitor, Sitagliptin (Januvia®) | |||||||||||||||||||||||
Medical condition: Short Bowel Syndrome with intestinal failure (SBS IF) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-000700-26 | Sponsor Protocol Number: 178-CL-203 | Start Date*: 2015-09-23 | ||||||||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | ||||||||||||||||||
Full Title: A multicentre, open-label, single dose, phase 1 study to evaluate the pharmacokinetics, safety and tolerability of mirabegron oral suspension in pediatric subjects from 3 to less than 12 years of a... | ||||||||||||||||||
Medical condition: -neurogenic detrusor overactivity (NDO) -overactive bladder (OAB) | ||||||||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003138-18 | Sponsor Protocol Number: UCC-Strider | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:University College Cork | |||||||||||||
Full Title: STRIDER Ireland: A Randomised Controlled Trial of Sildenafil Therapy In Dismal Prognosis Early‐Onset Intrauterine Growth Restriction | |||||||||||||
Medical condition: Severe early - onset Intrauterine Growth Restriction (IUGR), (also referred to as Fetal growth restriction) diagnosed between 22+0 and 29+6 gestational age. IUGR is defined as an estimated fetal we... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003125-21 | Sponsor Protocol Number: P170915J | Start Date*: 2020-03-23 |
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | ||
Full Title: EFFECT OF INTRAVENOUS IRON SUPPLEMENTATION ON CELIAC DISEASE REMISSION IN PATIENTS WITH IRON DEFICIENCY AND INTESTINAL VILLOUS ATROPHY: A RANDOMIZED TRIAL | ||
Medical condition: Celiac patients with iron deficiency and intestinal villous atrophy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-006179-20 | Sponsor Protocol Number: INSULINE | Start Date*: 2013-01-04 |
Sponsor Name:Endocrinology and Nutrition Unit. Hospital Universitari Bellvitge. | ||
Full Title: Comparative randomized clinical trial between insulin analogues and human insulin in hospitalized patients treated with enteral nutrition and who present hyperglycemia. INSULINE study. | ||
Medical condition: Pacients receiving enteral nutrition and who present hyperglycemia. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001739-21 | Sponsor Protocol Number: FiDoAp | Start Date*: 2012-03-26 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LO STUDIO E LA CURA DEI TUMORI - FONDAZIONE "G. PASCALE" | |||||||||||||
Full Title: A study of Sativex for pain Relief and appetite stimulation in Patients with advanced malignancy. Phase II | |||||||||||||
Medical condition: advanced malignant cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-000340-15 | Sponsor Protocol Number: 178-CL-202 | Start Date*: 2014-07-11 | ||||||||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | ||||||||||||||||||
Full Title: A multicentre, open-label, single ascending dose Phase 1 study to evaluate the pharmacokinetics, safety and tolerability of mirabegron OCAS tablets in pediatric subjects from 5 to less than 18 year... | ||||||||||||||||||
Medical condition: -neurogenic detrusor overactivity (NDO) -overactive bladder (OAB) | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) BE (Completed) NO (Completed) DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-000438-35 | Sponsor Protocol Number: CL 0600-004 | Start Date*: 2004-09-30 |
Sponsor Name:NPS Allelix Corporation | ||
Full Title: A study of the Efficacy and Safety of Teduglutide in subjects with Parenteral Nutritional Dependant Short Bowel Syndrome | ||
Medical condition: Short Bowel Syndrome (SBS) refers to the clinical situation whereby a significant reduction in the absorptive capacity of the intestine results from inadequate anatomical or functional length of re... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
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