Status:
COMPLETED
Study to Evaluate Anxiety Sensitivity and Somatic Symptoms as Risk Factors for PONV
Lead Sponsor:
Johannes Gutenberg University Mainz
Conditions:
Postoperative Nausea and Vomiting
Eligibility:
FEMALE
18-75 years
Brief Summary
This prospective observational study aims to evaluate the influence of somatic symptom load and anxiety sensitivity as risk factors for the occurrence of postoperative nausea and vomiting (PONV). Phys...
Eligibility Criteria
Inclusion
- female patients 18-75 years
- non-smokers
- must be able to give written informed consent
- planned surgical intervention requiring hospitalisation
- not included in another clinical trial
Exclusion
- emergency intervention
- total intravenous anesthesia (TIVA) with propofol
- disability to give written informed consent
- physical or psychic disorders requiring permanent psycho-social care
- no German language skills
Key Trial Info
Start Date :
October 1 2012
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
October 1 2013
Estimated Enrollment :
160 Patients enrolled
Trial Details
Trial ID
NCT01875120
Start Date
October 1 2012
End Date
October 1 2013
Last Update
November 11 2013
Active Locations (1)
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1
Johannes Gutenberg University Medical Center, Department of Anesthesiology
Mainz, Rhineland-Palatinate, Germany, 55131