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

Risikofaktorer for Postoperativ Smerte og Kvalme Etter Dagkirurgisk Gynekologisk Laparoskopi

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05050708
Enrollment
300
Registered
2021-09-20
Start date
2021-08-24
Completion date
2022-07-25
Last updated
2021-09-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postoperative Nausea, Postoperative Pain

Brief 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

Interventions

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

Sponsors

Oslo University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Elective adult patients due for planned ambulatory gynaecological laparoscopy * Must be able to speak and write in Norwegian language

Exclusion criteria

* Patients who, for some reason, is transferred to non-ambulatory (same day discharge) care. * Patients who, for some reason, have a change in surgical procedure from laparoscopy

Design outcomes

Primary

MeasureTime frameDescription
postoperative pain0-24 hoursNumerical Ratings Score (NRS) Scale 0-10, 10 is worst
postoperative nausea0-24 hoursyes/no, Numerical Rating Score (NRS), Scale 0-10, 10 is worst

Secondary

MeasureTime frameDescription
Post-op fatigue0-24 hrsChristensen score, 0-10, 10 is maximal fatigue
Post-op function0-24hrEveryday function
Peri-operative nausea risk scorepreop, 0-24 hours post-operativelyApfel score, 0-4 (4 is maximal risk).Based on a number of registrations, such as: smoking status, postoperative opioid effects, smoking status, travel sickness, previous nause or vomiting after surgery/anaesthesia
Post-op anti-emetic drug consumption0-24hrtype and dose of ante-emetic medication
Post-op analgesia consumption0-24hrnumber of opioid equivalents consumed
Peri-operative pain risk scorepreop, 0-24 hoursBased on a number of registrations, such as: age, sosio-economic status, pre-op pain, pre-op use of opioids, pre-op anxiety or depression, pre-op catastrophizing, pre-op expectations, type of surgery, type of anaesthesia, lenght/ivasive ness of surgery, peri-op drug consumtion

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026