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Riskfactors of Post-operative Pain and Nausea After Ambulatory Gynaecological Laparocopy.

NCT05050708 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2021-09-20

No results posted yet for this study

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

Conditions

  • Postoperative Pain
  • Postoperative Nausea

Interventions

OTHER

Patient interview

Patient will be interviewed pre-operatively and at 24 hrs post-opartively

Sponsors & Collaborators

  • Oslo University Hospital

    lead OTHER

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-08-24
Primary Completion
2022-06-25
Completion
2022-07-25

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05050708 on ClinicalTrials.gov