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Clinical Trials/EUCTR2010-018450-12-SE
EUCTR2010-018450-12-SE
Active, not recruiting
Not Applicable

Optimising pain control after caesarean section - an evaluation if oxycodone can replace morphine and low potency opioids postoperatively. - Cesarean section and pain control

Agneta Blanck Olerup0 sites80 target enrollmentJune 24, 2010
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ConditionsPain management after elective cesarean section.MedDRA version: 12.1Level: LLTClassification code 10036276Term: Postoperative analgesia
DrugsOxyContin 10 mgOxyContin 20 mgOxyNorm 5 mgOxyNorm 10 mg/ml

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain management after elective cesarean section.
Sponsor
Agneta Blanck Olerup
Enrollment
80
Status
Active, not recruiting
Last Updated
13 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 24, 2010
End Date
TBD
Last Updated
13 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Female

Investigators

Sponsor
Agneta Blanck Olerup

Eligibility Criteria

Inclusion Criteria

  • •Women undergoing elective cesarean section at the Karolinska University Hospital.
  • •Women who intend to breast feed.
  • •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

  • •Women with previous chronic pain, mental illness requiring medication, drug abuse or difficulties to communicate, severe pregnancy complications, premature delivery, medical disease that can be suspected to influence the wellbeing of the newborn baby, intolerance to opiates or other drugs used in the present study or participation in another clinical trial during the last month.

Outcomes

Primary Outcomes

Not specified

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