MedTrace Logo

Analgesia and Antihyperalgesia of Tramadol and Acetaminophen Per Oral After Caesarean Section

NCT00873743 · Status: SUSPENDED · Type: OBSERVATIONAL · Enrollment: 120

Last updated 2009-04-02

No results posted yet for this study

Summary

The aim of this study is to evaluate quality of patient-controlled peroral analgesia after cesarian section using the combination of tramadol and acetaminophen. Research hypothesis is that the combination reduces pain at leg rising more than tramadol alone.

Conditions

  • Pain
  • Cesarean Section

Sponsors & Collaborators

  • University Hospital Schleswig-Holstein

    collaborator OTHER

  • Medical University of Vienna

    lead OTHER

Principal Investigators

  • Stephan Kettner, MD, Prof · Department of Anesthesiology, General Intensive Care and Pain Control, Medical University Vienna

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2008-10-31
Primary Completion
2009-05-31
Completion
2009-10-31

Countries

  • Austria

Study Locations

More Related Trials

Entities

Diseases

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 NCT00873743 on ClinicalTrials.gov