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Sevoflurane, Propofol, Postoperative Pain

NCT01437462 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 168

Last updated 2013-04-10

No results posted yet for this study

Summary

The impact of anaesthetic method (intravenous vs. inhalational) has been proposed, but not proven in a large-scale study. The researchers aim to provide an investigation that has sufficient power to clarify the potential effect of anaesthetic method on postoperative need of opioids. Sevoflurane and propofol will be compared.

Conditions

  • Healthy Adults
  • Gynecological Disease

Interventions

DRUG

Sevoflurane

Sevoflurane inhalation anesthesia, sufficient amount to maintain adequate general anesthesia for surgery

DRUG

Propofol

Propofol intravenous anesthesia, sufficient amount to maintain adequate anesthesia during surgery

Sponsors & Collaborators

  • Tampere University Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
69 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-10-31
Primary Completion
2013-03-31
Completion
2013-03-31

Countries

  • Finland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01437462 on ClinicalTrials.gov