Trials / Unknown
UnknownNCT05050708
Riskfactors of Post-operative Pain and Nausea After Ambulatory Gynaecological Laparocopy.
Risikofaktorer for Postoperativ Smerte og Kvalme Etter Dagkirurgisk Gynekologisk Laparoskopi
- Status
- Unknown
- Phase
- —
- Study type
- Observational
- Enrollment
- 300 (estimated)
- Sponsor
- Oslo University Hospital · Academic / Other
- Sex
- Female
- Age
- 18 Years
- Healthy volunteers
- Not accepted
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
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Patient interview | Patient will be interviewed pre-operatively and at 24 hrs post-opartively |
Timeline
- Start date
- 2021-08-24
- Primary completion
- 2022-06-25
- Completion
- 2022-07-25
- First posted
- 2021-09-20
- Last updated
- 2021-09-20
Locations
1 site across 1 country: Norway
Source: ClinicalTrials.gov record NCT05050708. Inclusion in this directory is not an endorsement.