- Trials with a EudraCT protocol (18)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
18 result(s) found for: Medical bag.
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EudraCT Number: 2021-000058-24 | Sponsor Protocol Number: Connect&Go | Start Date*: Information not available in EudraCT |
Sponsor Name:Erasmus MC Cancer Institute | ||
Full Title: Administration of immune checkpoint inhibitors through an elastomeric pump. A patient preference study and cost analysis. | ||
Medical condition: Solid tumors for which nivolumab or pembrolizumab monotherapy is an EMA approved indication. This includes (but is not limited to) melanoma, renal-cell cancer, NSCLC and head and neck cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-001656-18 | Sponsor Protocol Number: INOCOV-19 | Start Date*: 2020-05-19 |
Sponsor Name:Oslo University Hospital | ||
Full Title: Inhaled Nitric Oxide As A Bridge To Mechanical Ventilation In Patients With Suspected Covid-19 Respiratory Failure | ||
Medical condition: Severe respiratory failure in patients with confirmed, suspected or probable Covid- 19 disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2009-016801-40 | Sponsor Protocol Number: IP-001-09 | Start Date*: 2016-01-26 | |||||||||||
Sponsor Name:IPERBOREAL PHARMA | |||||||||||||
Full Title: Efficacy and Safety assessments of a peritoneal dialysis solution containing Glucose, Xylitol and L-Carnitine compared to standard PD solutions in Continuous Ambulatory Peritoneal Dialysis (CAPD) | |||||||||||||
Medical condition: Patients with ESRD treated by CAPD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005298-23 | Sponsor Protocol Number: IP-002-05 | Start Date*: 2007-03-12 | |||||||||||
Sponsor Name:IPERBOREAL PHARMA | |||||||||||||
Full Title: Efficiency of L-Carnitine-containing Peritoneal Dialysis Solutions for diurnal exchanges in CAPD Patients with ESRD on Glucose and Lipid Metabolisms. Randomized, Parallel Study Compared versus a St... | |||||||||||||
Medical condition: Patients affected by End stage renal disease ESRD treated with Continuous Ambulatory Peritoneal Dialysis CAPD . | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005300-13 | Sponsor Protocol Number: IP-003-05 | Start Date*: 2007-05-29 | |||||||||||
Sponsor Name:IPERBOREAL PHARMA | |||||||||||||
Full Title: Efficiency of L-Carnitine-containing Peritoneal Dialysis Solutions for diurnal exchanges in diabetes type 2 CAPD patients with ESRD on glucose metabolism. Randomized, parallel study compared versus... | |||||||||||||
Medical condition: Patients affected by End Stage Renal Disease (ESRD) treated with Continuous Ambulatory Peritoneal Dialysis (CAPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002210-46 | Sponsor Protocol Number: LiSA | Start Date*: 2016-07-28 |
Sponsor Name:University Medical Centre RadboudUMC | ||
Full Title: Study: Reduces intravenous lidocaine the need for alfentanyl during colonoscopy under Procedural Sedation and Analgesia? | ||
Medical condition: patients with IBD, between 18 and 65 years, which are scheduled for a colonoscopy with PSA. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-023311-34 | Sponsor Protocol Number: CPA 368-10 | Start Date*: 2011-02-04 | |||||||||||
Sponsor Name:AOP Orphan Pharmaceuticals AG | |||||||||||||
Full Title: A prospective, randomized, double blinded, crossover, two-treatment, two-sequence, short term pharmacokinetic, pharmacodynamic and tolerability, single centre study to compare AOP200704 vs. Esmolol... | |||||||||||||
Medical condition: healthy male and female volunteers, intended for the treatment of dobutamine-induced tachycardia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-005144-14 | Sponsor Protocol Number: 01-CARDIONIDO | Start Date*: 2018-04-12 |
Sponsor Name:Dr. Forteza Gil | ||
Full Title: Comparative study of two types of cardioplegia during cardiac surgery in the adult patient | ||
Medical condition: Cardiac surgery | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005761-11 | Sponsor Protocol Number: AG0501CR | Start Date*: 2006-05-25 |
Sponsor Name:Australasian Gastro−Intestinal Trials Group | ||
Full Title: The MAX study: A randomised phase II/III study to evaluate the role of Mitomycin C, Avastin and Xeloda in patients with untreated metastatic colorectal cancer | ||
Medical condition: Previously untreated metastatic colorectal cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005365-35 | Sponsor Protocol Number: 1449 | Start Date*: 2008-07-20 | |||||||||||
Sponsor Name:Fresenius Medical Care Deutschland GmbH | |||||||||||||
Full Title: Multicentric, parallel, controlled, randomized, single blind clinical evaluation of a new low sodium peritoneal dialysis solution on patients with hypertension treated with continous ambulatory or... | |||||||||||||
Medical condition: Subjects with renal failure treated with peritoneal dialysis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) FR (Completed) DK (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004236-38 | Sponsor Protocol Number: 12250 | Start Date*: 2017-01-24 |
Sponsor Name:University of Oxford | ||
Full Title: OPtimising Treatment for MIld Systolic hypertension in the Elderly: a randomised controlled trial | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2011-006041-14 | Sponsor Protocol Number: FINA-007 | Start Date*: 2012-10-26 |
Sponsor Name:MerLion Pharmaceuticals GmbH | ||
Full Title: A Multi-Dose, Double-Blind, Double-Dummy, Active Control, Randomized Clinical (Phase II) Study of Two Dosing Regimens of Finafloxacin for the Treatment of cUTI and/or Acute Pyelonephritis Requiring... | ||
Medical condition: Complicated Urinary Tract Infection and/or Acute Polyonephritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: PL (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-003237-25 | Sponsor Protocol Number: POPPIV4.022.07.16 | Start Date*: 2015-08-21 |
Sponsor Name:University of Oxford | ||
Full Title: A blinded randomised placebo-controlled trial investigating the efficacy of morphine analgesia for procedural pain in infants | ||
Medical condition: Screening for Retinopathy of Prematurity is an essential yet painful routine test that is performed multiple times in infants who are born prematurely. Premature infants also regularly require heel... | ||
Disease: | ||
Population Age: Preterm newborn infants, Newborns, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-002384-42 | Sponsor Protocol Number: MRINZ/15/A1 | Start Date*: 2016-10-06 | |||||||||||
Sponsor Name:Medical Research Institute of New Zealand | |||||||||||||
Full Title: Randomised Controlled Trial of the efficacy and safety of an ICS/LABA reliever therapy regimen in asthma. | |||||||||||||
Medical condition: Asthma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004183-21 | Sponsor Protocol Number: IP-001-18 | Start Date*: 2022-08-19 | |||||||||||
Sponsor Name:Iperboreal Pharma Srl | |||||||||||||
Full Title: A Study to Evaluate the EffIcacy and Safety of XyloCore, a Glucose Sparing Experimental Solution, for Peritoneal Dialysis | |||||||||||||
Medical condition: End-Stage Renal Disease (ESRD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) IT (Trial now transitioned) DK (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005863-29 | Sponsor Protocol Number: HelmetHeparin | Start Date*: 2021-07-15 | |||||||||||||||||||||
Sponsor Name:ASST FATEBENEFRATELLI SACCO | |||||||||||||||||||||||
Full Title: Nebulised heparin in COVID-19-related ARDS patients undergoing non-invasive ventilation with helmet cPAP: a prospective, randomised, double blind, placebo-controlled, multicentre study | |||||||||||||||||||||||
Medical condition: COVID-19-related Acute Respiratory Distress Syndrome (ARDS) patients undergoing non-invasive ventilation with helmet continuous positive airway pressure (cPAP) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-004946-41 | Sponsor Protocol Number: SP-PP18 | Start Date*: 2019-09-12 |
Sponsor Name:Dr. Virgilio P. Carnielli, | ||
Full Title: Personalized versus standard parenteral nutrition for preterm infants with a birth weight greater than 1250 grams: a phase IV randomized clinical trial | ||
Medical condition: Growth of preterm infants with a birth weight greater than 1250g on parenteral nutrition. | ||
Disease: | ||
Population Age: Preterm newborn infants, Under 18 | Gender: Male, Female | |
Trial protocol: ES (Ongoing) IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001394-29 | Sponsor Protocol Number: 31998 | Start Date*: 2007-12-28 | |||||||||||
Sponsor Name:Baxter Healthcare Corporation | |||||||||||||
Full Title: Multi-center, prospective trial to demonstrate Improved Metabolic control of PPEN vs DDDD in DIAbetic CAPD patients -The IMPENDIA Trial | |||||||||||||
Medical condition: End stage renal disease patients with Diabetes Type I and II on Continuous Ambulatory Peritoneal Dialysis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) PT (Prematurely Ended) AT (Completed) IT (Prematurely Ended) CZ (Completed) ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
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