WHO ICTRP trial
Crystalloids or colloids in patients with severe sepsis: effects on hemodynamics…
EUCTR2006-004350-25-FR · EU Clinical Trials Register · Not Recruiting
Key facts
| Trial ID | EUCTR2006-004350-25-FR |
|---|---|
| Public title | Crystalloids or colloids in patients with severe sepsis: effects on hemodynamics and tolerability of enteral nutrition - CRYSTMAS protocol (CRYSTalloids Morbidity Associated with severe Sepsis) |
| Scientific title | Crystalloids or colloids in patients with severe sepsis: effects on hemodynamics and tolerability of enteral nutrition - CRYSTMAS protocol (CRYSTalloids Morbidity Associated with severe Sepsis) |
| Primary sponsor | Fresenius Kabi Deutschland GmbH |
| Registry | EU Clinical Trials Register |
| Recruitment status | Not Recruiting |
| Study type | Interventional clinical trial of medicinal product |
| Phase | Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): no Therapeutic confirmatory - (Phase III): yes Therapeutic use (Phase IV): no |
| Countries | France;Germany |
| Conditions | Severe sepsis MedDRA version: 8.1 Level: LLT Classification code 10040070 Term: Septic shock |
| Interventions | Trade Name: Voluven Pharmaceutical Form: Solution for infusion Concentration unit: g/l gram(s)/litre Concentration type: equal Concentration number: 60- Trade Name: Chlorure de sodium 0,9% Fresenius Pharmaceutical Form: Solution for… |
| Registration date | Dec 29, 2006 |
| Target size | 180 |
| Secondary IDs | 06-HE06-01 |
| Registry page | clinicaltrialsregister.eu |
At a glance
- Yes Results available
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About WHO ICTRP trial registrations
The WHO ICTRP combines trial registrations from primary registries worldwide into a single searchable index. Contact and ethics-committee details are not shown here.
Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: