WHO ICTRP trial

Behandling ved intraventrikulær blødning: Et pilotstudie af virkningen med…

EUCTR2008-008215-25-DK · EU Clinical Trials Register · Not Recruiting

Key facts

Trial ID EUCTR2008-008215-25-DK
Public title Behandling ved intraventrikulær blødning: Et pilotstudie af virkningen med tidlig intraventrikulær actilysebehandling.
Scientific title Behandling ved intraventrikulær blødning: Et pilotstudie af virkningen med tidlig intraventrikulær actilysebehandling.
Primary sponsor Walter Fischer
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): yes Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): no
Countries Denmark
Conditions 1. Subarachnoidal blødning (SAH) med intraventrikulær blødning(IVH) 2. Spontan intraventrikulær blødning (IVH) uden påvist blodkarmisdannelse (AVM) 3. Randomiserede kontroller med SAH og IVH 4. Randomiserede kontroller med IVH uden påvist…
Interventions Trade Name: Actilyse Product Name: Actilyse Product Code: B01AD02 Pharmaceutical Form: Injection* INN or Proposed INN: Alteplase Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 10- Pharmaceutical form of…
Registration date Jan 26, 2009
Target size 80
Secondary IDs H-A-2008-109
Registry page clinicaltrialsregister.eu

At a glance

  • No 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:

Browse all WHO ICTRP trial registrations