EUCTR2005-002110-38-SEActive, not recruitingNot Applicable
RCT of oral paracetamol for procedural anxiety, distress and pain in children with cancer - RCT oral paracetamol pedonc
Dept of ped hem/onc0 sites50 target enrollmentStarted: May 19, 2005Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Active, not recruiting
- Sponsor
- Enrollment
- 50
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional clinical trial of medicinal product
Eligibility Criteria
- Sex
- All
Inclusion Criteria
- •50 patienter som ska få nål i intravenös port på den barnonkologiska avdelningen eller mottagningen; vid Akademiska barnsjukhuset i Uppsala, vid Barnkliniken Universitetssjukhuset Linköping eller vid Astrid Lindgrens barnsjukhus i Stockholm ska inkluderas konsekutivt.
- •Are the trial subjects under 18? yes
- •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) no
- •F.1.3.1 Number of subjects for this age range
Exclusion Criteria
- •Exklusionskriterier: ålder =1 samt =20 år, barn med påtaglig smärta (> VAS 5 av annan orsak än nålsättning), barn som är känt stickrädda och som behöver sedering sedan tidigare (det skulle i dessa fall vara oetiskt att randomisera), feber >39º, uttalat illamående, uttalad leverpåverkan (> 10 ggr normalvärdet av transaminaser), interaktion (se bilaga FASS) med pågående behandling samt överkänslighet mot ingående aktiv substans.
Investigators
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