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 | 2005-001938-32 | EFFICACY, SAFETY, AND QUALITY OF LIFE OF A LONG-TERM HOME PARENTERAL NUTRITION REGIMEN WITH EITHER LIPIDEM® OR LIPOFUNDIN® MCT A MONO-CENTER, RANDOMIZED, DOUBLE BLIND STUDY | 2014-01-15 | due-trials |
| Completed, but no date | 2005-003350-99 | METABOLIC EFFECT OF RINGERFUNCIN B. BRAUN IN HEALTHY VOLUNTEERS AND COMPARISON WITH IONIC SOLUTION PLASMA-LYTE BAXTER | bad-data | |
| Not reported Terminated | 2005-003542-33 | Estudio prospectivo, multicéntrico, aleatorizado, comparativo, doble ciego, para evaluar dos emulsiones lipídicas diferentes en la nutrición parenteral total del enfermo crítico y su influencia en la ... | 2011-09-13 | due-trials |
| Reported results Terminated | 2006-001879-38 | Prospective, controlled, single-blind, bicentric, randomized study on the safety of HES 130/0.42 combined with a balanced electrolyte solution vs. 5% Albumin combined with an unbalanced electrolyte so... | 2010-08-25 | due-trials |
| Reported results | 2007-003571-39 | Prospective, monocentric, controlled, randomized, double-blind study to compare two different propofol emulsions regarding tolerability and injection pain during the induction of anesthesia in adults | 2008-09-24 | due-trials |
| Reported results | 2008-004175-22 | PROSPECTIVE, CONTROLLED, DOUBLE-BLIND, RANDOMIZED MULTICENTRIC STUDY ON THE EFFICACY AND SAFETY OF A TARGET CONTROLLED PLASMA VOLUME REPLACEMENT THERAPY WITH A HYPER-ONCOTIC BALANCED HES 130/0.42 SO... | 2013-07-11 | due-trials |
| Reported results Terminated | 2010-018524-58 | Prospective controlled double-blind phase III bicentre study on the efficacy and safety of a balanced gelatine solution in combination with a balanced electrolyte solution versus a standard gelatine s... | 2013-01-18 | due-trials |
| Not reported Terminated | 2011-003397-82 | Prospective, randomized, controlled, double-blind, parallel-group, mono-centre, explorative Phase IV trial on the efficacy and safety of a fish oil containing lipid emulsion versus a standard soybean ... | 2015-05-27 | due-trials |
| Not reported | 2015-000057-20 | PROSPECTIVE, RANDOMIZED, CONTROLLED, DOUBLE-BLIND, MULTI-CENTRIC, INTERNATIONAL, STUDY ON THE EFFICACY AND SAFETY OF AN EARLY TARGET CONTROLLED PLASMA VOLUME REPLACEMENT THERAPY WITH A BALANCED GELATI... | 2021-12-13 | due-trials |
| Listed as ongoing, but also has a completion date and reported results | 2015-000849-23 | A RANDOMIZED, CONTROLLED, DOUBLE-BLIND, MULTICENTER CLINICAL TRIAL ON HOME PARENTERAL NUTRITION USING AN OMEGA-3 FATTY ACID ENRICHED MCT/LCT LIPID EMULSION | 2022-07-19 | bad-data |
| 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 |