- Trials with a EudraCT protocol (4)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
4 result(s) found for: Extravascular space.
Displaying page 1 of 1.
| EudraCT Number: 2008-000069-41 | Sponsor Protocol Number: THCHOG-2008-01 | Start Date*: 2008-04-09 |
| Sponsor Name:Erasmus MC | ||
| Full Title: Regulation of colloid osmotic pressure during cardiopulmonary bypass in infants: prospective randomised trial | ||
| Medical condition: Regulation of COP during CPB in infants | ||
| Disease: | ||
| Population Age: Preterm newborn infants, Newborns, Infants and toddlers, Under 18 | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| 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: 2006-001414-33 | Sponsor Protocol Number: RGHT 000275 | Start Date*: 2006-08-01 |
| Sponsor Name:The Royal Group Hospitals Trust | ||
| Full Title: The effect of hydroxyl-methyl coenzyme A reductase inhibition (statins) in patients with acute lung injury(ALI) and the acute respiratory distress syndrome(ARDS) | ||
| Medical condition: Acute Lung Injury (ALI) and the Acute Respiratory Distress Syndrome (ARDS) | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2014-003408-65 | Sponsor Protocol Number: | Start Date*: 2016-08-26 | ||||||||||||||||
| Sponsor Name:University of Edinburgh [...] | ||||||||||||||||||
| Full Title: Ulipristal acetate versus conventional management of heavy menstrual bleeding (HMB; including uterine fibroids): a randomised controlled trial and exploration of mechanism of action (UCON trial) | ||||||||||||||||||
| Medical condition: Heavy menstrual bleeding | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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Query did not match any studies.