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Clinical Trial Summary

Patient due for elective, ambulatory gynaecological laparoscopy will be screened peri-operatively for known and potential risk factors of postoperative pain and nausea/vomiting. The actual incidence and severity of pain and nausea/vomiting will be recorded during th 0-24 hr intervall after end of surgery, as well as the doses of all drugs, given for either prophylaxis or treatment


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05050708
Study type Observational
Source Oslo University Hospital
Contact
Status Recruiting
Phase
Start date August 24, 2021
Completion date July 25, 2022

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