Postoperative Analgesie and Antihyperalgesia of Tramadol and Acetaminophen peroral after Caesarean Section - Tramalstudie
- Conditions
- Pain after Cesarean Section in spinal anesthesia
- Registration Number
- EUCTR2007-005231-28-AT
- Lead Sponsor
- Med. Univ. Wien, Universitätsklinik für Anästhesie, allgemeine Intensivmedizin und Schmerzmedizin
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Recruiting
- Sex
- Female
- Target Recruitment
- 120
Inclusion Criteria
Female patients between 18 and 45 years, ASA-Status 1-2, BMI 19-29, that are scheduled for planned caesarean section and have given written informed consent, will be included
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) no
F.1.3.1 Number of subjects for this age range
Exclusion Criteria
Exclusion criteria are known 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.
Study & Design
- Study Type
- Interventional clinical trial of medicinal product
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method