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Leikkauksen jälkeisen kivun voimakkuus propofoli- tai sevofluraanianestesian jälkeen.

Leikkauksen jälkeisen kivun voimakkuus propofoli- tai sevofluraanianestesian jälkeen.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
EU CTR
Registry ID
EUCTR2008-001125-34-FI
Enrollment
Unknown
Registered
2008-03-28
Start date
2008-05-08
Completion date
Unknown
Last updated
2013-05-27

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

Conditions

Potilaat tulevat tähystyksessä tehtävään kohdunpoistoleikkaukseen. MedDRA version: 9.1 Level: LLT Classification code 10021151 Term: Hysterectomy

Interventions

Trade Name: Propofol-Lipuro Pharmaceutical Form: INN or Proposed INN: Propofolum Trade Name: Sevorane 100% Pharmaceutical Form: INN or Proposed INN: Sevofluranum

Sponsors

Arvi Yli-Hankala
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime 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