DOM- A comparative study with pre-emptive parenteral oxycodone, morphine and dexamethasone in the treatment of postoperative pain in paediatric patients 4 to 12 years of age.

Status

Not yet recruiting

Phases

Unknown

Study type

Interventional

Source

EU CTR

Registry ID

EUCTR2008-003705-13-FI

Enrollment

100

Registered

2010-01-25

Start date

2010-01-25

Completion date

Unknown

Last updated

2012-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

paediartic asa 1-2 patients admitted for tonsillectomy MedDRA version: 9.1 Level: LLT Classification code 10044006 Term: Tonsillectomy

Interventions

Trade Name: Oxynorm (oxycodone) or other generic product chosen to the hospital Pharmaceutical Form: Solution for injection INN or Proposed INN: OXYCODONE HYDROCHLORIDE CAS Number: 124903 Pharmaceutic

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Are the trial subjects under 18? yes Number of subjects for this age range: F.1.2 Adults (18-64 years) F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Main Objective: ;Secondary Objective: ;Primary end point(s):	—

Countries

Finland

Outcome results

None listed

Source: EU CTR (via WHO ICTRP) · Data processed: Feb 4, 2026