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Clinical Trials/EUCTR2008-001052-48-IE
EUCTR2008-001052-48-IE
Active, Not Recruiting
N/A

A Comparison of the Post-operative analgesic effects of Propofol anaesthesia with Sevoflurane anaesthesia

Coombe Women and Infants University Hospital0 sites80 target enrollmentMarch 3, 2008
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ConditionsAcute post-operative painMedDRA version: 9.1Level: LLTClassification code 10066714Term: Acute painMedDRA version: 9.1Level: LLTClassification code 10036286Term: Post-operative pain
DrugsDiprivanSevorane

Overview

Phase
N/A
Intervention
Not specified
Conditions
Acute post-operative pain
Sponsor
Coombe Women and Infants University Hospital
Enrollment
80
Status
Active, Not Recruiting
Last Updated
14 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 3, 2008
End Date
TBD
Last Updated
14 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Female

Investigators

Sponsor
Coombe Women and Infants University Hospital

Eligibility Criteria

Inclusion Criteria

  • •American Society of Anesthesiologist classification I and II patients; aged over 18 years undergoing laparoscopic day case surgery.
  • •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

  • •Chronic pain states; known allergies or contraindications to the study medications; lack of informed consent; currently pregnant; currently breast feeding

Outcomes

Primary Outcomes

Not specified

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