WHO ICTRP trial

Oral Versus Intravenous Dexamethasone in Community-acquired pneumonia study

NL-OMON36192 · Overview of Medical Research in the Netherlands (NL-OMON) · Not Recruiting

Key facts

Trial ID NL-OMON36192
Public title Oral Versus Intravenous Dexamethasone in Community-acquired pneumonia study
Scientific title Oral Versus Intravenous Dexamethasone in Community-acquired pneumonia study - OVID study
Primary sponsor Sint Antonius Ziekenhuis
Registry Overview of Medical Research in the Netherlands (NL-OMON)
Recruitment status Not Recruiting
Study type Interventional
Phase 4
Countries Netherlands
Conditions lower respiratory tract infection Pneumonia;10024970;lower respiratory tract infection;Pneumonia
Interventions Subjects will be assigned to 6 mg dexamethasone starting dose administered PO, followed by 3 times 6 mg dexamethasone PO once daily or 5,26 mg dexamethasonedisodiumphosphate (= 4 mg dexamethasone) starting dose administered IV, followed by…
Registration date Jun 30, 2011
Target size 30
Secondary IDs 2011-002346-12;NL36999.100.11;volgt na goedkeuring
Registry page onderzoekmetmensen.nl

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