Status:
SUSPENDED
Analgesia and Antihyperalgesia of Tramadol and Acetaminophen Per Oral After Caesarean Section
Lead Sponsor:
Medical University of Vienna
Collaborating Sponsors:
University Hospital Schleswig-Holstein
Conditions:
Pain
Cesarean Section
Eligibility:
FEMALE
18-45 years
Brief 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 combina...
Detailed Description
Caesarean section rate is growing in western countries (from 9% by 1980, to 12% by 1990 up to 22-24% in 2002)1. Pain after Caesarean section involves 2 components, somatic pain from the wound and vis...
Eligibility Criteria
Inclusion
- 18 and 45 years
- ASA-Status 1-2
- BMI 19-29, that are scheduled for planned caesarean section and have given written informed consent
Exclusion
- Allergies or hypersensitivities to evaluated drugs
- History of pain syndrome
- Substance abuse
- Preeclampsia or eclampsia
- Deviation from standardised surgical procedure
- Treatment with magnesium sulfate
- Renal or hepatic impairment and deviations from the standardized anaesthetic treatment
Key Trial Info
Start Date :
October 1 2008
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
October 1 2009
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT00873743
Start Date
October 1 2008
End Date
October 1 2009
Last Update
April 2 2009
Active Locations (1)
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1
Medical University Vienna
Vienna, Vienna, Austria, 1080