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Clinical Trials/EUCTR2009-011038-82-AT
EUCTR2009-011038-82-AT
Active, not recruiting
Phase 1

Postoperative pain after anesthesia: propofol vs. sevoflurane

Medizinsche Universität Wien, Univ.Klinik f. Anästhesie u. Allgem. Intensivmedizin0 sites90 target enrollmentJune 8, 2010
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Conditionspostoperativ pain
DrugsDiprivan PFS 1 % (500 mg/50 ml)-FertigspritzeSevorane-Inhalationsnarkotikum

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
postoperativ pain
Sponsor
Medizinsche Universität Wien, Univ.Klinik f. Anästhesie u. Allgem. Intensivmedizin
Enrollment
90
Status
Active, not recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
June 8, 2010
End Date
March 13, 2014
Last Updated
4 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Medizinsche Universität Wien, Univ.Klinik f. Anästhesie u. Allgem. Intensivmedizin

Eligibility Criteria

Inclusion Criteria

  • •patients having a stripping operation for varicosis veins
  • •weight \<100 ,BMI \< 35
  • •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

  • •patient´s with chronic pain

Outcomes

Primary Outcomes

Not specified

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