WHO ICTRP trial
Relation dose-effet du propofol: comparaison en double aveugle des différentes…
EUCTR2009-012898-36-FR · EU Clinical Trials Register · Authorised
Key facts
| Trial ID | EUCTR2009-012898-36-FR |
|---|---|
| Public title | Relation dose-effet du propofol : comparaison en double aveugle des différentes - Les Propofols |
| Scientific title | Relation dose-effet du propofol : comparaison en double aveugle des différentes - Les Propofols |
| Primary sponsor | Hopital Foch |
| Registry | EU Clinical Trials Register |
| Recruitment status | Authorised |
| Study type | Interventional clinical trial of medicinal product |
| Countries | France |
| Conditions | general anesthesia MedDRA version: 9.1 Level: LLT Classification code 10002323 Term: Anesthesia general |
| Interventions | Trade Name: Propofol Frésenius 10 mg/ml Product Name: Propofol Pharmaceutical Form: Intravenous infusion Trade Name: Propofol-Lipuro Product Name: Propofol Pharmaceutical Form: Intravenous infusion Trade Name: Diprivan 10 mg/ml Product… |
| Registration date | Jul 17, 2009 |
| Target size | 210 |
| Secondary IDs | 2009/22 |
| Registry page | clinicaltrialsregister.eu |
At a glance
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About WHO ICTRP trial registrations
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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date: