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

University of Oslo (UIO) logo

University of Oslo (UIO)

Status

Unknown

Conditions

Postoperative Pain
Postoperative Nausea

Treatments

Other: Patient interview

Study type

Observational

Funder types

Other

Identifiers

NCT05050708
Gyn.smerte.op.risiko.21

Details and patient eligibility

About

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

Enrollment

300 estimated patients

Sex

Female

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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