Riskfactors of Post-operative Pain and Nausea After Ambulatory Gynaecological Laparocopy.
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- STATUS
- Recruiting
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- participants needed
- 300
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- sponsor
- Oslo University Hospital
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
Details
Condition | Pain, Postoperative pain, Post-Operative Nausea and Vomiting, Post-Surgical Pain, Vomiting, Pain (Pediatric), Postoperative Nausea |
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Age | 18years - 100years |
Treatment | Patient Interview |
Clinical Study Identifier | NCT05050708 |
Sponsor | Oslo University Hospital |
Last Modified on | 21 September 2021 |
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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