All clinical trials on the European Union Clinical Trials Register (EUCTR) must report their results in the registry within a year of completion. This site tracks who's doing this and who isn't. Learn more »
These trials completed more than 12 months ago and should have reported results. Some have, some have not.
These trials are not yet due to report results: some are ongoing, some completed within the past 12 months.
These trials have problematic data on the registry. Details why »
| Status | Trial ID | Title | Completion date | Category |
|---|---|---|---|---|
| Reported results | 2004-001805-90 | Efficacy and security of glutamine dipeptide (Dipeptiven®) - Supplemented parenteral nutrition in critic patients. Double blind, randomized, multicenter study. | 2007-05-25 | due-trials |
| Reported results | 2004-002108-14 | Multizentrische Studie mit einer Niedrig-Natrium Peritonealdialyse-Lösung bei hypertensiven od. antihypertensiv behandelten CAPD Patienten auf balance Lösung | 2006-05-15 | due-trials |
| Completed, but no date, and reported results | 2004-002724-17 | Efficacy of Neodolpasse™ in the treatment of postoperative pain: Morphine sparing effect during the first 24 hours postoperatively after unilateral total hip arthroplasty. | bad-data | |
| Reported results | 2005-002425-31 | A double-blind, randomised study comparing the safety and tolerance of SMOFlipid 20% and Intralipid 20% in long-term treatment with parenteral nutrition | 2008-10-24 | due-trials |
| Reported results | 2006-002589-20 | Evaluación del acetato de calcio / carbonato de magnesio (OsvaRen®) en comparación con el sevelamer (Renagel®) en pacientes sometidos a hemodiálisis | 2009-03-25 | due-trials |
| Reported results | 2006-004350-25 | Crystalloids or colloids in patients with severe sepsis: effects on hemodynamics and tolerability of enteral nutrition | 2010-05-27 | due-trials |
| Reported results | 2007-005365-35 | Multicenter, parallel, controlled, randimized, single-blind clinical evaluation of new low sodium peritoneal dialysis solution on patients with hypertension treated with continuous ambulatory or autom... | 2014-10-28 | due-trials |
| Reported results | 2007-006065-32 | Evaluation of the efficacy of 6% hydroxyethyl starch (HES, 130/0.4) in normal saline compared to Ringer’s lactate solution for the prevention of hypotension during spinal anaesthesia for caesarean sec... | 2009-12-17 | due-trials |
| Reported results | 2008-000429-20 | A randomised, double-blind study evaluating the safety, tolerability, and amino acid plasma levels of Neoven compared to Vaminolact in infants after surgical interventions. | 2009-12-18 | due-trials |
| Reported results | 2008-006749-18 | Efficacy and safety of 6 % hydroxyethyl starch 130/0.4 (Voluven®) vs. 5% HSA in volume replacement therapy during elective open-heart surgery in paediatric patients | 2010-08-05 | due-trials |
| Reported results | 2009-009427-11 | Efecto de la solución de diálisis peritoneal balance sobre la membrana peritoneal de pacientes tratados con diálisis peritoneal automatizada (DPA) (The effect of balance peritoneal dialysis solution o... | 2012-12-27 | due-trials |
| Reported results Terminated | 2009-012602-39 | A randomised, double-blind study evaluating the safety, tolerability, protein accretion, amino acid plasma levels and long-term outcome of Neoven compared to Vaminolact(R) in premature very low birth ... | 2011-03-15 | due-trials |
| Reported results | 2009-012603-26 | A randomised, double-blind study evaluating the safety, tolerability and clinical outcome of Neoven compared to Vaminolact in premature ELBW infants | 2011-03-18 | due-trials |
| Reported results Terminated | 2009-012604-92 | A randomised, double-blind study of the safety and efficacy of Neoven compared to Vaminolact in infants and children requiring long-term parenteral nutrition | 2011-03-18 | due-trials |
| Reported results | 2011-005734-18 | Prospective randomised controlled open-label explorative multi-centre pilot trial of Volulyte®-supplemented versus Albumin-supplemented fluid resuscitation for major burns | 2013-09-13 | due-trials |
| Reported results | 2012-004178-24 | Study to investigate the therapeutic equivalence of OsvaRen® tablets and OsvaRen® granules | 2015-04-30 | due-trials |
| Reported results | 2012-005701-43 | Therapeutic Equivalence Study of Propofol Using Target-Controlled Infusion of Propofol 2% (20 mg/mL) MCT Fresenius Compared with Diprivan® 20 mg/mL (AstraZeneca) in Patients Undergoing Elective Surger... | 2014-02-13 | due-trials |
| Listed as ongoing, but also has a completion date and reported results | 2016-002162-30 | Prospective, randomized, controlled, double-blind, multicentre, multinational study on the safety and efficacy of 6% Hydroxyethyl starch (HES) solution versus an electrolyte solution in patients unde... | 2022-07-06 | bad-data |
| Listed as ongoing, but also has a completion date and reported results | 2016-002176-27 | 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 in ... | 2022-06-25 | bad-data |
| Not reported Terminated | 2017-001559-30 | Efficacy of long-term parenteral nutrition with SmofKabiven® E concomitant to chemo- and/or immunotherapy: A prospective, randomised, controlled, open, multicentre, two-stage, adaptive clinical trial ... | 2019-04-05 | due-trials |
| Reported results Terminated | 2017-001972-46 | Reaching Protein Target with SmofKabiven extra Nitrogen Versus Olimel N9E: A Prospective, Randomised, Active-controlled, Patient-blinded, Multicentre Clinical Trial During the Early Phase of Acute Cri... | 2020-09-07 | due-trials |
| Reported results | 2017-003555-35 | A Multicentre, Randomised, Open-label, Parallel-Group Pilot Study to Evaluate the Efficacy of Patiromer in Optimising Mineralocorticoid Receptor Antagonist Therapy in Heart Failure Subjects with Hyper... | 2019-10-31 | due-trials |
| Reported results | 2018-002359-14 | Blood Glucose Response After Oral Intake of Lactulose (Laevolac®) in Mildly Constipated Patients with Diabetes Mellitus Type 2 | 2019-03-05 | due-trials |
| Reported results | 2019-004369-42 | A Randomized, Double-Blind, Multiple-Dose, Parallel-Group, Two-Arm Study to Evaluate the Efficacy, Safety and Immunogenicity of MSB11456 Compared to European Union approved RoActemra® in Patients with... | 2022-06-06 | due-trials |
| Completed, report not yet due | 2020-004422-31 | A Double-blind, Randomized, Multicenter, Multiple-dose, 2-arm, Parallel-group Study to Evaluate Efficacy, Pharmacodynamics, Safety, and Immunogenicity of FKS518 - Proposed Biosimilar to Denosumab with... | 2023-08-07 | not-yet-due |