Viewing Study NCT05050708



Ignite Creation Date: 2024-05-06 @ 4:40 PM
Last Modification Date: 2024-10-26 @ 2:13 PM
Study NCT ID: NCT05050708
Status: UNKNOWN
Last Update Posted: 2021-09-20
First Post: 2021-08-23

Brief Title: Riskfactors of Post-operative Pain and Nausea After Ambulatory Gynaecological Laparocopy
Sponsor: Oslo University Hospital
Organization: Oslo University Hospital

Study Overview

Official Title: Risikofaktorer for Postoperativ Smerte og Kvalme Etter Dagkirurgisk Gynekologisk Laparoskopi
Status: UNKNOWN
Status Verified Date: 2021-09
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Patient due for elective ambulatory gynaecological laparoscopy will be screened peri-operatively for known and potential risk factors of postoperative pain and nauseavomiting

The actual incidence and severity of pain and nauseavomiting 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None